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Viscoplast™ Gaza opatrunkowa jałowa

EUDAMED

Class I (EU MDR)

Ref not applicable

by 3M Deutschland GmbH (Medical)

Identity

Trade Name
Viscoplast™ Gaza opatrunkowa jałowa EUDAMED
Device Name
Viscoplast™ Kompresy jałowe EUDAMED
Model / Reference
not applicable EUDAMED

Identifiers

Primary DI / UDI-DI
05902658662140 EUDAMED
Basic UDI-DI
06082232761050000000020GD EUDAMED
EMDN Code
M020199 COTTON GAUZES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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™ Gaza opatrunkowa jałowa 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 918dafa5-4a59-4ec3-bb6c-1668982d03d2 61 fields · synced Oct 7, 2026