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Bone Conductor B81

FDA UDI

Class II (US FDA UDI)

by PATH medical GmbH

Identity

Trade Name
Bone Conductor B81 FDA UDI
Generic Name
Evoked-potential audiometer FDA UDI
Device Name
Bone conductor with patient response button for Sentiero FDA UDI
Model / Reference
100910 FDA UDI
Description
Bone conductor with patient response button for Sentiero FDA UDI

Identifiers

Primary DI / UDI-DI
04260223143120 FDA UDI
510(k) Number
K133012 FDA UDI
FDA Product Code
GWJ FDA UDI
EWO FDA UDI
GMDN Term
Evoked-potential audiometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1900 FDA UDI
874.1050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Evoked-potential audiometer

Bone Conductor B81 by PATH medical GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Evoked-potential audiometer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PATH medical GmbH

Sources (1)

  • FDA UDI 55f9ead4-b56e-4ac9-b5f6-1d65dee291c7 34 fields · synced May 30, 2026