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Nylon Head Impactor for Femoral Head (spare head for femoral head impactor)
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Nylon Head Impactor for Femoral Head (spare head for femoral head impactor) FDA UDI
- Generic Name
- Orthopaedic implant impactor, reusable FDA UDI
- Model / Reference
- PN0475 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05056405503566 FDA UDI
- FDA Product Code
- HWA FDA UDI
- GMDN Term
- Orthopaedic implant impactor, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
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
Category: Orthopaedic implant impactor, reusable
Nylon Head Impactor for Femoral Head (spare head for femoral head impactor) by Platts & Nisbett Limited — Class I — FDA UDI — listed in FDA GUDID
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Platts & Nisbett Limited
Sources (1)
- FDA UDI b3330edd-f97b-46ef-915d-081a3893b10f 32 fields · synced Jun 8, 2026