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STERI•PORE voděodolná náplast

EUDAMED

Class I (EU MDR)

Ref 0956/5

by STERIWUND spol. s r.o.

Identity

Device Name
STERI•PORE voděodolná náplast EUDAMED
Model / Reference
0956/5 EUDAMED

Identifiers

Primary DI / UDI-DI
08595154110733 EUDAMED
Basic UDI-DI
85951541021VC 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•PORE 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 49f2a424-e0ed-42ad-b0dc-a709113a3aee 61 fields · synced Jun 19, 2026