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KREWI-mull

EUDAMED

Class I (EU MDR)

Ref 600004

by KOB GmbH

Identity

Trade Name
KREWI-mull EUDAMED
Device Name
564 EUDAMED
Model / Reference
600004 EUDAMED

Identifiers

Primary DI / UDI-DI
04004221065486 EUDAMED
Basic UDI-DI
4004221564XL EUDAMED
Unit of Use DI
04004221021437 EUDAMED
EMDN Code
M0303010101 ELASTIC FIXING BANDAGES, NON-ADHESIVE, EXTENSIBLE IN ONE DIRECTION 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

KREWI-mull by KOB 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

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Manufacturer

Manufacturer
KOB GmbH
EUDAMED SRN
DE-MF-000005043

Sources (1)

  • EUDAMED 6858d708-bc17-47fb-86f0-9c16a4099766 61 fields · synced Jul 17, 2026