Identity
- Trade Name
- GRU Femur FDA UDI
- Generic Name
- Uncoated unicondylar knee femur prosthesis FDA UDI
- Device Name
- GRU Femur RMLL Size 3 FDA UDI
- Model / Reference
- GRU-RM/LL-3F-C FDA UDI
- Description
- GRU Femur RMLL Size 3 FDA UDI
Identifiers
- Catalog Number
- GRU-RM/LL-3F-C FDA UDI
- Primary DI / UDI-DI
- 09340499005522 FDA UDI
- 510(k) Number
- K051721 FDA UDI
- FDA Product Code
- HRY FDA UDI
- GMDN Term
- Uncoated unicondylar knee femur prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3530 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
GRU Femur by Global Manufacturing Technology Pty Limited — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Global Manufacturing Technology Pty Limited
Sources (1)
- FDA UDI 75ba24ee-7abf-4b9f-973e-cd6d55087062 38 fields · synced Jun 1, 2026