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Nicholson Cement Removal Osteotome 5mm
EUDAMEDFDA UDIClass I (EU MDR)
Ref 5251-05
Identity
- Trade Name
- Nicholson Cement Removal Osteotome 5mm EUDAMEDInnomed, Inc. FDA UDI
- Generic Name
- Orthopaedic osteotome FDA UDI
- Device Name
- Osteotome EUDAMEDNicholson Cement Removal Osteotome 5mm FDA UDI
- Model / Reference
- 5251-05 EUDAMEDFDA UDI
- Description
- Nicholson Cement Removal Osteotome 5mm FDA UDI
Identifiers
- Catalog Number
- 5251-05 FDA UDI
- Primary DI / UDI-DI
- 00840277110961 EUDAMEDFDA UDI
- Basic UDI-DI
- 8402771INNOOSTEO016V EUDAMED
- Direct Marketing DI
- 00840277110961 EUDAMED
- FDA Product Code
- HWM FDA UDI
- EMDN Code
- L090401 ORTHOPAEDIC SURGERY OSTEOTOMES, REUSABLE EUDAMED
- GMDN Term
- Orthopaedic osteotome 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
Nicholson Cement Removal Osteotome 5mm 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 | 8402771INNOOSTEO016V | 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 f89599c9-72ea-4e35-8ed8-21b78c12943a 61 fields · synced Jul 14, 2026
- FDA UDI 2b9f5a50-b93b-4ece-8b07-c246c0e5ac1c 34 fields · synced May 30, 2026