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VACUETTE® Venenstauer
EUDAMEDClass I (EU MDR)
Ref 5000K002B (Kunden-REF 840050)
by Kimetec GmbH
Identity
- Trade Name
- VACUETTE® Venenstauer EUDAMED
- Device Name
- CBC Tourniquet EUDAMED
- Model / Reference
- 5000K002B (Kunden-REF 840050) EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250373650609 EUDAMED
- Basic UDI-DI
- 42503736001KC EUDAMED
- EMDN Code
- V9003 TOURNIQUETS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria 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
Category: Limb tourniquet, manual, reusable
VACUETTE® Venenstauer by Kimetec GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Limb tourniquet, manual, reusable.
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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 | 42503736001KC | Class I | Active |
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Manufacturer
- Manufacturer
- Kimetec GmbH
- EUDAMED SRN
- DE-MF-000006493
Sources (1)
- EUDAMED ae693e9e-cbe2-466e-949c-4c6609181f2f 61 fields · synced Jul 27, 2026