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Global Apg+
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 2236-00-021Model Shoulder Glenoid Fossa Prosthesis Trial
Identity
- Trade Name
- GLOBAL APG+ EUDAMEDFDA UDI
- Generic Name
- Shoulder glenoid fossa prosthesis trial FDA UDI
- Device Name
- Shoulder Glenoid Fossa Prosthesis Trial EUDAMEDGLOBAL APG+ TRIAL SIZE 52 FDA UDI
- Model / Reference
- Shoulder Glenoid Fossa Prosthesis Trial EUDAMED2236-00-021 EUDAMEDFDA UDI
- Description
- GLOBAL APG+ TRIAL SIZE 52 FDA UDI
Identifiers
- Catalog Number
- 223600021 FDA UDI
- Primary DI / UDI-DI
- 10603295105886 EUDAMEDFDA UDI
- Basic UDI-DI
- 0603295a001017V EUDAMED
- Direct Marketing DI
- 10603295105886 EUDAMED
- FDA Product Code
- HWT FDA UDI
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Shoulder glenoid fossa prosthesis trial FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 888.4800 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
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
Global Apg+ by DePuy Ireland UC — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0603295a001017V | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- DePuy Ireland UC
- EUDAMED SRN
- IE-MF-000007377
Sources (2)
- EUDAMED 3d6ed434-251b-4bae-81b4-ff913532a924 61 fields · synced May 30, 2026
- FDA UDI b312c7f7-44ba-4584-b3f2-5709bc6a8d7c 35 fields · synced May 30, 2026