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Askina Forte

EUDAMED

Class I (EU MDR)

Ref 9057021

by KOB GmbH

Identity

Trade Name
Askina Forte EUDAMED
Device Name
104 EUDAMED
Model / Reference
9057021 EUDAMED

Identifiers

Primary DI / UDI-DI
04004221006243 EUDAMED
Basic UDI-DI
4004221104WE EUDAMED
EMDN Code
M0304010201 ELASTIC COMPRESSION BANDAGES, COHESIVE, LOW EXTENSIBILITY (<70%) 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

Askina Forte 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 53acee31-e386-4a0f-a35a-8f581208788a 61 fields · synced Jun 18, 2026