Identity
- Trade Name
- Baha 5 SuperPower Earhook 2+ (M) FDA UDI
- Generic Name
- Direct acoustic cochlear implant system FDA UDI
- Device Name
- Retention device to hold Baha 5 SuperPower sound processor in Under-the-Ear position (UTE) FDA UDI
- Model / Reference
- P1173607 FDA UDI
- Description
- Retention device to hold Baha 5 SuperPower sound processor in Under-the-Ear position (UTE) FDA UDI
Identifiers
- Catalog Number
- P1173607 FDA UDI
- Primary DI / UDI-DI
- 09321502051422 FDA UDI
- FDA Product Code
- LXB FDA UDI
- GMDN Term
- Direct acoustic cochlear implant system 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Direct acoustic cochlear implant system
Baha 5 SuperPower Earhook 2+ (M) by Cochlear Bone Anchored Solutions AB — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Direct acoustic cochlear implant system.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Cochlear Bone Anchored Solutions AB
Sources (1)
- FDA UDI 9cb29979-b431-4264-9547-44c80ab98e6c 35 fields · synced May 31, 2026