Baha 5 SuperPower Processing unit, Demo 96000

by Cochlear Bone Anchored Solutions AB

Baha 5 SuperPower Processing unit, Demo 96000 is a Class II device made by Cochlear Bone Anchored Solutions AB, listed in FDA GUDID since 24 Oct 2016 (UDI-DI 09321502033794), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number09321502033794 UDI-DI	Date24 Oct 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 09321502033794

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Baha 5 SuperPower Processing unit, Demo
Generic name: Bone-conduction hearing implant system sound processor/vibrator
Model / Ref / Catalog: 96000

Primary DI / UDI-DI: 09321502033794
FDA product code: LXB
GMDN term: Bone-conduction hearing implant system sound processor/vibrator

Device class: Class II
Regulation number: 874.3302
GUDID distribution status: In Commercial Distribution

Similar devices in this category

Other devices filed under Bone-conduction hearing implant system sound processor/vibrator.

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See all devices from Cochlear Bone Anchored Solutions AB →

Properties

Prescription use
Serial number
Expiration date
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Other properties (11, all answered No)