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Viscoplast™ Turystyczny

EUDAMED

Class I (EU MDR)

Ref V0-26-5TPModel V12M3Z24

by 3M Deutschland GmbH (Medical)

Identity

Trade Name
Viscoplast™ Turystyczny EUDAMED
Device Name
Viscoplast ™ Zestaw Uniwersalny EUDAMED
Model / Reference
V12M3Z24 EUDAMED
V0-26-5TP EUDAMED

Identifiers

Primary DI / UDI-DI
04064035157678 EUDAMED
Basic UDI-DI
06082232761050000000008GP EUDAMED
EMDN Code
M04010101 NON-WOVEN ADHESIVE DRESSINGS, WITH ABSORBENT PAD 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

Viscoplast™ Turystyczny by 3M Deutschland GmbH (Medical) — 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-000011641

Sources (1)

  • EUDAMED dac5d356-6fd6-4105-961e-78145182aec4 61 fields · synced Oct 6, 2026