Identity
- Trade Name
- BIRMINGHAM HIP RESURFACING (BHR) FDA UDI
- Generic Name
- General internal orthopaedic fixation system implantation kit FDA UDI
- Device Name
- BHR 42MM SLEEVE RING FDA UDI
- Model / Reference
- 90120142 FDA UDI
- Description
- BHR 42MM SLEEVE RING FDA UDI
Identifiers
- Catalog Number
- 90120142 FDA UDI
- Primary DI / UDI-DI
- 03596010594280 FDA UDI
- PMA Number
- P040033 FDA UDI
- FDA Product Code
- NXT FDA UDI
- GMDN Term
- General internal orthopaedic fixation system implantation kit FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: General internal orthopaedic fixation system implantation kit
Birmingham Hip Resurfacing (bhr) by Smith & Nephew, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as General internal orthopaedic fixation system implantation kit.
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Cleared under the same submission
P040033 also covers:
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
- BIRMINGHAM HIP — Smith & Nephew, Inc.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI cfaf0680-6ee4-4c5b-a45b-bd7f457bc4fb 36 fields · synced Jun 8, 2026