Identity
- Trade Name
- CHARNLEY FDA UDI
- Generic Name
- Wire twister FDA UDI
- Device Name
- CHARNLEY WIRE TIGHTENER FDA UDI
- Model / Reference
- 9622-42-000 FDA UDI
- Description
- CHARNLEY WIRE TIGHTENER FDA UDI
Identifiers
- Catalog Number
- 962242000 FDA UDI
- Primary DI / UDI-DI
- 10603295241676 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Wire twister FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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 bc3a11d5-6f72-4706-a785-e3aec1ea3465 36 fields · synced Jun 1, 2026