Screw Clamp
FDA UDIEUDAMEDClass I (US FDA UDI)
by Hpf Srl
Identity
- Trade Name
- SKRUEPINCETTER EUDAMEDSCREW CLAMP FDA UDI
- Generic Name
- Orthopaedic implant/instrument assembling device FDA UDI
- Model / Reference
- 9095.10.115 EUDAMEDFDA UDIScrew clamp EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08057968719187 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08057968719187 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L091399 ORTHOPAEDIC SURGERY FORCEPS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Orthopaedic implant/instrument assembling device FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- Italy EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
Yes
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
No
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Orthopaedic implant/instrument assembling device
Screw Clamp by Hpf Srl — Class I — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
MDD
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Hpf Srl
Sources (2)
- FDA UDI 84491a99-d9e7-4c8d-b9b2-82cf571da8f7 32 fields · synced Aug 5, 2026
- EUDAMED 31cd909c-7c2b-4a6c-b277-ce4d018a23b9 61 fields · synced Aug 5, 2026