Identity
- Trade Name
- Cormet FDA UDI
- Generic Name
- Resurfacing metallic hip prosthesis FDA UDI
- Model / Reference
- 479.248B FDA UDI
Identifiers
- Catalog Number
- 479.248B FDA UDI
- Primary DI / UDI-DI
- 05055196919457 FDA UDI
- PMA Number
- P050016 FDA UDI
- FDA Product Code
- NXT FDA UDI
- GMDN Term
- Resurfacing metallic hip prosthesis FDA UDI
Classification
- Device Class
- Class III 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
MR Conditional FDA UDI
Cormet by Corin Ltd — Class III — 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 III | Pending data |
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Manufacturer
- Manufacturer
- Corin Ltd
Sources (1)
- FDA UDI 18cc3f1c-a33e-41f9-b386-07cb53e6d8fa 35 fields · synced Jun 8, 2026