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AppliFix Foot

EUDAMED

Class I (EU MDR)

Ref 19720978

by KOB GmbH

Identity

Trade Name
AppliFix Foot EUDAMED
Device Name
777 EUDAMED
Model / Reference
19720978 EUDAMED

Identifiers

Primary DI / UDI-DI
04004221075751 EUDAMED
Basic UDI-DI
4004221777Y7 EUDAMED
Unit of Use DI
04004221023370 EUDAMED
EMDN Code
M03030199 ELASTIC FIXING BANDAGES - OTHER 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

AppliFix Foot 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 929cb89f-04ec-48f9-8bb7-3ab90d31b9ed 61 fields · synced Jul 21, 2026