Identity
- Device Name
- Dermatom EUDAMED
- Model / Reference
- 07495-31 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04063058001999 EUDAMED
- Basic UDI-DI
- 4063058000001974H EUDAMED
- Direct Marketing DI
- 04063058001999 EUDAMED
- EMDN Code
- Z120103 DERMOTOMY EQUIPMENT 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
Dermatom by REDA Instrumente GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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 | 4063058000001974H | Class I | Active |
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Manufacturer
- Manufacturer
- REDA Instrumente GmbH
- EUDAMED SRN
- DE-MF-000005592
Sources (1)
- EUDAMED 5f8f4ae3-1ee4-44a9-aace-8f99b12f78f0 61 fields · synced Aug 1, 2026