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Cbc Vecos®

EUDAMED

Class I (EU MDR)

Ref 521018

by Kimetec GmbH

Identity

Trade Name
CBC VECOS® EUDAMED
Device Name
CBC Tourniquet EUDAMED
Model / Reference
521018 EUDAMED

Identifiers

Primary DI / UDI-DI
14250373655915 EUDAMED
Basic UDI-DI
42503736001KC EUDAMED
EMDN Code
V9003 TOURNIQUETS 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

Category: Limb tourniquet, manual, reusable

Cbc Vecos® by Kimetec GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Limb tourniquet, manual, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Kimetec GmbH
EUDAMED SRN
DE-MF-000006493

Sources (1)

  • EUDAMED e36c74ed-d0c9-459e-9486-fa8563f22184 61 fields · synced Aug 3, 2026