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Viscoplast™ prestopor supermiękki

EUDAMED

Class I (EU MDR)

Ref not applicable

by 3M Deutschland GmbH (Medical)

Identity

Trade Name
Viscoplast™ prestopor supermiękki EUDAMED
Device Name
Viscoplast™ prestopor supermiękki EUDAMED
Model / Reference
not applicable EUDAMED

Identifiers

Primary DI / UDI-DI
04064035061166 EUDAMED
04064035061173 EUDAMED
05902658312182 EUDAMED
05902658312199 EUDAMED
Basic UDI-DI
06082232761050000000007GM 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™ prestopor supermiękki 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 (4)

  • EUDAMED 0dede58a-6982-4b02-bb8a-3b6bb6880046 61 fields · synced Oct 8, 2026
  • EUDAMED ffde5530-06a9-4ae2-9277-774a696bf7e9 61 fields · synced May 17, 2026
  • EUDAMED eac00373-5fa4-4135-acab-0c3cd586027e 61 fields · synced May 18, 2026
  • EUDAMED fe19cadd-9f41-4064-9f5e-aece2dcd6d36 61 fields · synced May 19, 2026