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E13C2 (9029) High-res. Broad Bandwidth, Endfire Transducer

bk3000E13C2 (9029) High-res. Broad Bandwidth, Endfire Transducer

9029/ View Product Page

Applicable Documents:

Print Table

Cleaning Agent

Compatibility

Compatibility Type

Comments

Cleaning d Footnote:
d) STERIS SYSTEM 1, SYSTEM 1 PLUS, and SYSTEM 1 Express have not been market cleared by the FDA.

3E-Zyme (Manual Cleaning)

Yes

Validated

—

3E-Zyme (Automated use)

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Bodedex forte

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

CIDEZYME XTRA Multi-Enzymatic Detergent/ CIDEZYME GL Enzymatic Detergent

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Gigazyme

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Intercept Wipes/Intercept Detergent

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Korsolex Endo-Cleaner 0,5%

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

MATRIX Biofilm Remover

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Neodisher MediClean Forte

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

pH neutral (pH 6-8), non-corrosive cleaning products intended for medical devices

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Prolystica 2x concentration. Enzymatic

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Revital-Ox Bedside Complete/2X Concentrate Enzymatic Detergent/Enzymatic Detergents

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Sekusept MultiEnzyme P

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Suma Med Enzyme

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Disinfection d Footnote:
d) STERIS SYSTEM 1, SYSTEM 1 PLUS, and SYSTEM 1 Express have not been market cleared by the FDA.

Medivators Advantage Plus Intercept (detergent), Rapicide PA Disinfectant flush: 70% isopropyl alcohol

Yes

Validated

Automated disinfection

Korsolex Basic (Manual Disinfection)

Yes

Validated

—

Tristel Fuse for Instruments (Tristel Fuse for Stella)

Yes

Validated

Manual Disinfection

Revital-Ox Resert/Resert XL HLD

Yes

Validated

Manual Disinfection

Ethanol 70% (wiping)

Yes

Validated

Manual Disinfection

Accel Prevention (wipes, ready-to-use liquid, concentrate)

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Adaspor Single Shot

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Antigermix S1

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Astra VR (with approved disinfectant)

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Bomix Plus

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Cavi Wipes/CaviCide

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Cidex OPA

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Cleanisept Wipes Forte

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Gigasept FF

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Glutaraldehyde 2% – 3.4%

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Incidin OxyFoam/Incidin OxyWipe S

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Isopropanol 70% (wiping)

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Korsolex Basic (Automated use)

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Korsolex Endo Disinfectant 1%/Korsolex Extra

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Meliseptol Foam

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Meliseptol Wipes Sensitive

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Metricide OPA Plus

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Mikrobac Tissues

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Mikrozoid AF Liquid

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Neodisher Endo Sept GA

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Neodisher Endo SEPT PAC/Neodisher Septo PAC

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Neodisher Septo DN

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Nu-Cidex

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

OPAL

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Rapicide/Rapicide OPA/28

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Rely+On Perasafe

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Revital-Ox Resert / Resert XL HLD (Automated use)

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Sani Cloth Plus Wipes/Sani Cloth Super Wipes

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Sekusept Aktiv

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Steranios 2%, 2% N.G., 2% E.C.S

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Thermosept PAA

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Tristel Duo for Ultrasound/Tristel Trio Wipe System

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

Trophon EPR / Trophon 2

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

Fit transducer completely above line mark.

Sterilization

STERIS System 1, 1E, 1 Plus and 1 Express c Footnote:
c) Follow product manufacturer's instructions and do not exceed transducer-specified limits. See Care and Cleaning Guide for more information. , d Footnote:
d) STERIS SYSTEM 1, SYSTEM 1 PLUS, and SYSTEM 1 Express have not been market cleared by the FDA.

Yes

Validated

—

STERIS V-Pro 1 Plus, V-Pro 60Non lumen cycle c Footnote:
c) Follow product manufacturer's instructions and do not exceed transducer-specified limits. See Care and Cleaning Guide for more information.

Yes

Validated

—

STERIS V-Pro maXNon lumen cycle or Flexible cycle c Footnote:
c) Follow product manufacturer's instructions and do not exceed transducer-specified limits. See Care and Cleaning Guide for more information.

Yes

Validated

—

Sterrad NX & 100NXStandard cycle c Footnote:
c) Follow product manufacturer's instructions and do not exceed transducer-specified limits. See Care and Cleaning Guide for more information.

Yes

Validated

—

Sterrad 100 NX Express Cycle

Yes

Validated

—

Sterrad 100SOne cycle only (USA),Short cycle (rest of the world) c Footnote:
c) Follow product manufacturer's instructions and do not exceed transducer-specified limits. See Care and Cleaning Guide for more information.

Yes

Validated

—

Sterrad 200Short cycle c Footnote:
c) Follow product manufacturer's instructions and do not exceed transducer-specified limits. See Care and Cleaning Guide for more information.

Yes

Validated

—

Matachana 130LF, Webeco FA90, Webeco FA95 (60°C cycle) c Footnote:
c) Follow product manufacturer's instructions and do not exceed transducer-specified limits. See Care and Cleaning Guide for more information.

Yes

Validated

Use a suitable connector lid and valve from the system manufacturer. See page 46 in the Care and Cleaning guide.

RENO-20/RENO-30/RENO-D50: ECO Cycle

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

RENO-S90, RENO-S130, RENO-S130D: ECO Cycle

No

—

—

RENO-S90, RENO-S130, RENO-S130D: Non Lumen Cycle

Yes

Material Compatible

a Footnote:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.

—

View Footnotes
Footnotes:
a) This table of reprocessing methods only indicates that BK Medical has evaluated the transducers for material compatibility, when reprocessed according to the product/system IFU, and not for their efficacy in attaining the appropriate level of reprocessing. Ensure that the reprocessing chamber is an appropriate size for the transducer.
b) Transducer connector is not immersible
c) Follow product manufacturer's instructions and do not exceed transducer-specified limits. See Care and Cleaning Guide for more information.
d) STERIS SYSTEM 1, SYSTEM 1 PLUS, and SYSTEM 1 Express have not been market cleared by the FDA.
e) Transducer has not been licensed by Health Canada
*Follow local regulations for minimum reprocessing. Check table 4 on page 29 of the Care and Cleaning Guide.
*Cleaning is an important first step for all transducer types. Every transducer used in a critical procedure must be sterilized as the final reprocessing step.

Information in this document is subject to change without notice.

Printed on 01/26/2022

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