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STERI•FILM transparentní, voděodolná náplast

EUDAMED

Class I (EU MDR)

Ref 0957/100

by STERIWUND spol. s r.o.

Identity

Device Name
STERI•FILM transparentní, voděodolná náplast EUDAMED
Model / Reference
0957/100 EUDAMED

Identifiers

Primary DI / UDI-DI
08595154111723 EUDAMED
Basic UDI-DI
85951541020VA EUDAMED
EMDN Code
M0599 MEDICAL PLASTERS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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

STERI•FILM transparentní, voděodolná náplast by STERIWUND spol. s r.o. — 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
CZ-MF-000036963

Sources (1)

  • EUDAMED 552019ae-4908-4ff3-84b8-62eebadd6c84 61 fields · synced Jun 18, 2026