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Subtrochanteric Femur Fracture Reduction Clamp
EUDAMEDFDA UDIClass I (EU MDR)
Ref 3850
Identity
- Trade Name
- Subtrochanteric Femur Fracture Reduction Clamp EUDAMEDInnomed, Inc. FDA UDI
- Generic Name
- Bone approximation clamp FDA UDI
- Device Name
- Forceps EUDAMEDSubtrochanteric Femur Fracture Reduction Clamp FDA UDI
- Model / Reference
- 3850 EUDAMEDFDA UDI
- Description
- Subtrochanteric Femur Fracture Reduction Clamp FDA UDI
Identifiers
- Catalog Number
- 3850 FDA UDI
- Primary DI / UDI-DI
- 00840277123893 EUDAMEDFDA UDI
- Basic UDI-DI
- 8402771INNOFORCEP01TM EUDAMED
- Direct Marketing DI
- 00840277123893 EUDAMED
- FDA Product Code
- HXD FDA UDI
- EMDN Code
- L091399 ORTHOPAEDIC SURGERY FORCEPS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Bone approximation clamp FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Subtrochanteric Femur Fracture Reduction Clamp by Innomed, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 8402771INNOFORCEP01TM | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Innomed, Inc.
- EUDAMED SRN
- US-MF-000014761
- Authorised Representative
- MediMark Europe Sarl. FR-AR-000000182
Sources (2)
- EUDAMED 44d029a8-1cd7-4c0b-86a6-de28dfb72cfb 61 fields · synced Jul 27, 2026
- FDA UDI 94d69dbd-bd71-45c5-b137-6e5981e1cde0 34 fields · synced May 29, 2026