Identity
- Trade Name
- Revival Modular Hip Stem FDA UDI
- Generic Name
- Revision uncoated hip femur prosthesis FDA UDI
- Device Name
- Distal Component 240mm Length; 21mm Diameter FDA UDI
- Model / Reference
- 120376021 FDA UDI
- Description
- Distal Component 240mm Length; 21mm Diameter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08033466132154 FDA UDI
- FDA Product Code
- MEH FDA UDILZO FDA UDI
- GMDN Term
- Revision uncoated hip femur prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3353 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: Revision uncoated hip femur prosthesis
Revival Modular Hip Stem by Corin Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- ZMR® — Zimmer, Inc. · Class II
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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
- Corin Ltd
Sources (1)
- FDA UDI 18f223d2-7f86-4008-a86d-494e0267ca25 33 fields · synced May 30, 2026