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Obinadlo hydrofilní pletené, nesterilní

EUDAMED

Class I (EU MDR)

Ref 0173

by STERIWUND spol. s r.o.

Identity

Trade Name
Obinadlo hydrofilní pletené, nesterilní EUDAMED
Device Name
OBVAZ HYDROFILNÍ PLETENÝ, nesterilní EUDAMED
Model / Reference
0173 EUDAMED

Identifiers

Primary DI / UDI-DI
08595154102257 EUDAMED
Basic UDI-DI
85951541004VC EUDAMED
EMDN Code
M030101 HYDROPHILIC GAUZE BANDAGES 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

Obinadlo hydrofilní pletené, nesterilní 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 05983656-7938-4fab-b8d1-0875886b6e5a 61 fields · synced Jun 19, 2026