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Indicator for Baha Attract

FDA UDI

Class I (US FDA UDI)

by Cochlear Bone Anchored Solutions AB

Identity

Trade Name
Indicator for Baha Attract FDA UDI
Generic Name
General external orthopaedic fixation system implantation kit, reusable FDA UDI
Device Name
N/A FDA UDI
Model / Reference
93571 FDA UDI
Description
N/A FDA UDI

Identifiers

Catalog Number
93571 FDA UDI
Primary DI / UDI-DI
09321502025362 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
General external orthopaedic fixation system implantation kit, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General external orthopaedic fixation system implantation kit, reusable

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

Similar devices

Also classified as General external orthopaedic fixation system implantation kit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cochlear Bone Anchored Solutions AB

Sources (1)

  • FDA UDI e261531d-0880-427c-93a0-04ec831325a3 35 fields · synced Jun 8, 2026