Identity
- Trade Name
- Comprehensive Reverse Shoulder Mini Baseplate FDA UDI
- Generic Name
- Reverse shoulder head prosthesis trial FDA UDI
- Model / Reference
- SSI002749 FDA UDI
Identifiers
- Catalog Number
- SSI002749 FDA UDI
- Primary DI / UDI-DI
- 00887868243905 FDA UDI
- FDA Product Code
- KWS FDA UDI
- GMDN Term
- Reverse shoulder head prosthesis trial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3660 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
No
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
Category: Reverse shoulder head prosthesis trial
Comprehensive Reverse Shoulder Mini Baseplate by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Reverse shoulder head prosthesis trial.
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- REUNION — Stryker Corp. · Class II
- Arthrex® — Arthrex, Inc. · Class II
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
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI e4f5190f-40d0-49dc-b140-4841f683bd74 35 fields · synced Jun 6, 2026