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Obvaz hydrofilní pletený, sterilní

EUDAMED

Class I (EU MDR)

Ref 0200

by STERIWUND spol. s r.o.

Identity

Trade Name
Obvaz hydrofilní pletený, sterilní EUDAMED
Device Name
Obvazy, sterilní EUDAMED
Model / Reference
0200 EUDAMED

Identifiers

Primary DI / UDI-DI
08595154102004 EUDAMED
Basic UDI-DI
8595154201OBVAZDG EUDAMED
EMDN Code
M030102 NON-WOVEN BANDAGES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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

Obvaz hydrofilní pletený, sterilní 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 77ccc63f-8daa-449a-a5df-0beaa7940f00 61 fields · synced Jun 18, 2026