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Medial Malleolus Fracture Reduction Aid
EUDAMEDFDA UDIClass I (EU MDR)
Ref 3664
Identity
- Trade Name
- Medial Malleolus Fracture Reduction Aid EUDAMEDInnomed, Inc. FDA UDI
- Generic Name
- Surgical drill guide, reusable FDA UDI
- Device Name
- Guide EUDAMEDMedial Malleolus Fracture Reduction Aid FDA UDI
- Model / Reference
- 3664 EUDAMEDFDA UDI
- Description
- Medial Malleolus Fracture Reduction Aid FDA UDI
Identifiers
- Catalog Number
- 3664 FDA UDI
- Primary DI / UDI-DI
- 00840277127389 EUDAMEDFDA UDI
- Basic UDI-DI
- 8402771INNOGUIDE01VS EUDAMED
- Direct Marketing DI
- 00840277127389 EUDAMED
- FDA Product Code
- FZX FDA UDI
- EMDN Code
- L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE EUDAMED
- GMDN Term
- Surgical drill guide, reusable 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
Medial Malleolus Fracture Reduction Aid 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 | 8402771INNOGUIDE01VS | 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 e3ec7d4f-76f3-49af-8541-38edc7f5d615 61 fields · synced Jul 8, 2026
- FDA UDI d92f462b-ec00-49ab-ac06-172f02e453a6 34 fields · synced May 30, 2026