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Baha

FDA UDI

Class I (US FDA UDI)

by Cochlear Bone Anchored Solutions AB

Identity

Trade Name
Baha FDA UDI
Generic Name
Surgical power tool system control unit, line-powered FDA UDI
Device Name
Spray clip (for Osscora handpiece), 3pcs FDA UDI
Model / Reference
91891 FDA UDI
Description
Spray clip (for Osscora handpiece), 3pcs FDA UDI

Identifiers

Catalog Number
91891 FDA UDI
Primary DI / UDI-DI
09321502020978 FDA UDI
FDA Product Code
GEY FDA UDI
GMDN Term
Surgical power tool system control unit, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical power tool system control unit, line-powered

Baha by Cochlear Bone Anchored Solutions AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical power tool system control unit, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 04f06871-e107-4087-b2b0-397d16cc23b6 35 fields · synced Jun 6, 2026