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Fixierpflaster Transparent

EUDAMED

Class I (EU MDR)

Ref 02-089

by WUNDmed GmbH & Co. KG

Identity

Trade Name
Fixierpflaster Transparent EUDAMED
Device Name
Pflaster EUDAMED
Model / Reference
02-089 EUDAMED

Identifiers

Primary DI / UDI-DI
04260206620112 EUDAMED
Basic UDI-DI
426020662apf1F5 EUDAMED
Direct Marketing DI
04260206620112 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

Fixierpflaster Transparent 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 5c8bc851-abc8-4e48-ab2c-39ffc203c7c5 61 fields · synced Oct 6, 2026