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Kombi-Box

EUDAMED

Class I (EU MDR)

Ref 05-004

by WUNDmed GmbH & Co. KG

Identity

Trade Name
Kombi-Box EUDAMED
Device Name
Pflaster EUDAMED
Model / Reference
05-004 EUDAMED

Identifiers

Primary DI / UDI-DI
04260206627364 EUDAMED
Basic UDI-DI
426020662apf1F5 EUDAMED
Direct Marketing DI
04260206627364 EUDAMED
EMDN Code
M0599 MEDICAL PLASTERS - 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

Kombi-Box by WUNDmed GmbH & Co. KG — 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

EUDAMED SRN
DE-MF-000010322

Sources (1)

  • EUDAMED 0b675fcc-6ed5-4625-a7ae-34a2d99558b8 61 fields · synced Jun 19, 2026