Identity
- Trade Name
- Duocentric® FDA UDI
- Generic Name
- Reverse shoulder prosthesis body FDA UDI
- Device Name
- Humeral baseplate FDA UDI
- Model / Reference
- 50263 FDA UDI
- Description
- Humeral baseplate FDA UDI
Identifiers
- Catalog Number
- 30210040 FDA UDI
- Primary DI / UDI-DI
- 03663703000769 FDA UDI
- FDA Product Code
- KWS FDA UDI
- GMDN Term
- Reverse shoulder prosthesis body 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Reverse shoulder prosthesis body
Duocentric® by Aston Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Reverse shoulder prosthesis body.
- BIO-MODULAR REVERSE SHOULDER — Biomet Orthopedics, Inc. · Class II
- Comprehensive® Reverse Shoulder — Biomet Orthopedics, Inc. · Class II
- Identity™ — Zimmer, Inc. · Class II
- GLOBAL UNITE — DEPUY (IRELAND) · Class II
- Comprehensive Reverse Shoulder — Biomet Orthopedics, Inc. · Class II
- Comprehensive® — Zimmer, Inc. · Class II
- Comprehensive® — Zimmer, Inc. · Class II
- Comprehensive® — Zimmer, 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
- Aston Medical
Sources (1)
- FDA UDI 2763780e-c2fc-4083-89de-3564b845fa7f 36 fields · synced May 30, 2026