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Kompressen

EUDAMED

Class I (EU MDR)

Ref 03-010

by WUNDmed GmbH & Co. KG

Identity

Trade Name
Kompressen EUDAMED
Device Name
Bandagen-Familie EUDAMED
Model / Reference
03-010 EUDAMED

Identifiers

Primary DI / UDI-DI
04260206625322 EUDAMED
Basic UDI-DI
426020662shb6HR EUDAMED
Direct Marketing DI
04260206625322 EUDAMED
EMDN Code
M0201020102 COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, NON-STERILE 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

Kompressen 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 8e1aa59b-7282-485b-a014-aa05c1a320e6 61 fields · synced Jul 12, 2026