Cleaning Information
Correct reprocessing is fundamental in guarding against infection. To make liquid-based reprocessing more convenient, most BK Medical transducers come with a special watertight plug lid to allow the entire transducer (including the cable and plug) to be fully submerged.
BK Medical equipment is designed to be durable but as devices are complex, care is needed when handling them.
BK Medical continuously validates and evaluates different reprocessing agents and methods.
To download the care and cleaning guide with reprocessing posters, select your language
Care and Cleaning Methods for Transducers
Follow local regulations for minimum reprocessing. Check table 4 on page 29 of the Care and Cleaning Guide.
Follow product manufacturer’s instructions and do not exceed transducer specified limits. See Care and Cleaning Guide for more information.
Click the transducer to read the information.
I13C3f (9076) Advanced Laparoscopic Transducer
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
N20P6 (9007) Minimally Invasive Transducer
N20P6 (9007) Minimally Invasive Transducer d Footnote: d) Transducer has not been licensed by Health Canada.
Print Cleaning MethodsEfficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Rob12C4 (9096) Robotic Transducer
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
I12C5 (9034) Mini-T Intraoperative Transducer
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
5P1e (9087) Phased Array Transducer
5P1e (9087) Phased Array Transducer b Footnote: b) Transducer connector is not immersible.
Print Cleaning MethodsEfficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
X18L5s (9009) Hockey Stick Transducer
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
14L3e (9086) Linear Transducer
14L3e (9086) Linear Transducer b Footnote: b) Transducer connector is not immersible.
Print Cleaning MethodsEfficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
E11C3b (9008) High-resolution biplane Transducer
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
3D X14L4 (9038) Endocavity Transducer
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
E13C2 (9029) High-res. Broad Bandwidth, Endfire Transducer
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
18L5s (9081) Small High-Frequency Linear Transducer
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
T7P2m (9027) TEE Transducer
- submersible
- not submersible, wiping only
- not submersible, wiping only
Validated Methods
3E-Zyme
CIVCO UltrOx HLD
Revital-Ox Resert XL HDL
Material Compatible Methods
Mild pH neutral detergent
Mild pH neutral detergent wipe
Mild pH neutral detergent wipe
Aniosyme DD1
Clinell Sporicidal wipes
Tristel Trio Wipes System
Cidex ADS, OPA and Nu-Cidex
Ethanol (EtOH) 70% wipes
Ethanol 70% wipes
Cidezyme / Enzol
Isopropyl alcohol (IPA) 70% wipes
IPA 70% wipes
Empower
Mikrozid® PAA wipes
Gigasept AF, Gigasept FF (Neu) and Gigasept PAA concentrate
Sani-Cloth AF3 wipes
Korsolex extra
Tristel Trio Wipes System
Metricide, Metricide 28, Metricide OPA Plus and Metricide Plus 30
Metrizyme
Neodisher MediClean forte/ Neodisher Septo 3000
Perasafe
Prolystica 2x conc.
Revital-Ox Resert XL HDL
Sekusept Aktiv
Steranios 2%, 2% N.G., 2% E.C.S
TD100 & TD5
Tristel Trio Wipe System
Wavicide 01
Warning: Extra care must be taken when cleaning this transducer, as there is no automatic cleaning system that can reprocess the entire transducer.
5C1e (9085) Curved Array Transducer
5C1e (9085) Curved Array Transducer b Footnote: b) Transducer connector is not immersible.
Print Cleaning MethodsEfficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicates that BK Medical has evaluated the device’s material compatibility with the reprocessing method when reprocessed according to the product/system IFU. Efficacy is not covered by this statement.
Efficacy validated by BK
Material Compatible a Footnote: a) “Material compatible” indicate