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Urgolast universal

EUDAMED

Class I (EU MDR)

Ref 603180

by KOB GmbH

Identity

Trade Name
Urgolast universal EUDAMED
Device Name
599 EUDAMED
Model / Reference
603180 EUDAMED

Identifiers

Primary DI / UDI-DI
04004221052608 EUDAMED
Basic UDI-DI
4004221599Y7 EUDAMED
Unit of Use DI
04004221022137 EUDAMED
EMDN Code
M030402010101 ELASTIC SUPPORT BANDAGES, NON-ADHESIVE, EXTENSIBLE IN ONE DIRECTION, HIGH EXTENSIBILITY 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

Urgolast universal 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 b588a041-bff8-479b-9737-eec3a2bef7e4 61 fields · synced Aug 1, 2026