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Baha Programming Cable Short Blue

FDA UDI

Class II (US FDA UDI)

by Cochlear Bone Anchored Solutions AB

Identity

Trade Name
Baha Programming Cable Short Blue FDA UDI
Generic Name
Bone-conduction hearing implant system sound processor/vibrator FDA UDI
Device Name
Baha Programming Cable Short Blue Spare FDA UDI
Model / Reference
91911 FDA UDI
Description
Baha Programming Cable Short Blue Spare FDA UDI

Identifiers

Catalog Number
91911 FDA UDI
Primary DI / UDI-DI
09321502016681 FDA UDI
510(k) Number
K142907 FDA UDI
FDA Product Code
LXB FDA UDI
GMDN Term
Bone-conduction hearing implant system sound processor/vibrator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3302 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: Bone-conduction hearing implant system sound processor/vibrator

Baha Programming Cable Short Blue by Cochlear Bone Anchored Solutions AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-conduction hearing implant system sound processor/vibrator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0adeb796-b8f1-4704-8886-03004d037c43 36 fields · synced May 31, 2026