Identity
- Trade Name
- CBC Percuflex EUDAMED
- Device Name
- CBC Percuflex EUDAMED
- Model / Reference
- 920390 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250373600277 EUDAMED
- Basic UDI-DI
- 42503736003KG EUDAMED
- EMDN Code
- L160101 NEUROLOGICAL HAMMERS, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
CBC Percuflex by Kimetec 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 | 42503736003KG | Class I | Active |
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Manufacturer
- Manufacturer
- Kimetec GmbH
- EUDAMED SRN
- DE-MF-000006493
Sources (1)
- EUDAMED a4f3feec-f657-4229-87fc-c057536e5d9f 61 fields · synced Jun 19, 2026