Identity
- Trade Name
- LIGHTENED TRIAL HEAD D50 mm FDA UDI
- Generic Name
- Femoral head prosthesis trial FDA UDI
- Model / Reference
- H0050051510 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08057968716445 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Femoral head prosthesis trial 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Femoral head prosthesis trial
LIGHTENED TRIAL HEAD D50 mm by Hpf Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- G7® — Biomet Orthopedics, Inc. · Class II
- AcuMatch — Exactech, Inc. · Class I
- NovoHip Total Hip System — Novosource, Inc. · Class II
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
- Hpf Srl
Sources (1)
- FDA UDI 41414357-dabf-4f8c-9f48-98e8dbc680be 32 fields · synced Jun 1, 2026