Identity
- Trade Name
- Affiniti FDA UDI
- Generic Name
- Shoulder glenoid fossa prosthesis trial FDA UDI
- Device Name
- PEGGED GLENOID TRIAL FDA UDI
- Model / Reference
- 9000203 FDA UDI
- Description
- PEGGED GLENOID TRIAL FDA UDI
Identifiers
- Catalog Number
- 9000203 FDA UDI
- Primary DI / UDI-DI
- 00846832024421 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Shoulder glenoid fossa prosthesis trial FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- Not 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
Moist Heat or Steam Sterilization FDA UDI
Affiniti by Tornier, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
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Manufacturer
- Manufacturer
- Tornier, Inc.
Sources (1)
- FDA UDI 2fc430da-9d83-45ab-af8d-76879297089d 37 fields · synced May 30, 2026