Identity
- Trade Name
- CHARNLEY FDA UDI
- Generic Name
- Bone curette, reusable FDA UDI
- Device Name
- CHARNLEY CURETTE MED FDA UDI
- Model / Reference
- 9620-46-000 FDA UDI
- Description
- CHARNLEY CURETTE MED FDA UDI
Identifiers
- Catalog Number
- 962046000 FDA UDI
- Primary DI / UDI-DI
- 10603295240860 FDA UDI
- FDA Product Code
- HTF FDA UDI
- GMDN Term
- Bone curette, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not 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
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
Charnley by Depuy International Ltd — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Depuy International Ltd
Sources (1)
- FDA UDI 4c416c44-9ee4-41b7-aedc-bd374fe9e2be 36 fields · synced May 31, 2026