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208-020-0603
EUDAMEDClass I (EU MDR)
Ref 208-020-0603Model Surgical Instruments
Identity
- Model / Reference
- Surgical Instruments EUDAMED208-020-0603 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250869634786 EUDAMED
- Basic UDI-DI
- 42508696000010019G EUDAMED
- EMDN Code
- L091099 OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
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
Category: Surgical implant template, reusable
208-020-0603 by Biedermann Motech GmbH & Co. KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 42508696000010019G | Class I | Active |
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Manufacturer
- Manufacturer
- Biedermann Motech GmbH & Co. KG
- EUDAMED SRN
- DE-MF-000005455
Sources (1)
- EUDAMED 219fe75a-9ecb-4421-9fe0-4b62053e0184 61 fields · synced Aug 1, 2026