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wound compress

EUDAMED

Class I (EU MDR)

Ref -

by Danyang Sunmed Healthcare Corporation

Identity

Device Name
wound compress EUDAMED
Model / Reference
- EUDAMED

Identifiers

Primary DI / UDI-DI
06974567461465 EUDAMED
Basic UDI-DI
697456746000125Z EUDAMED
Direct Marketing DI
06974567461465 EUDAMED
EMDN Code
M0202030101 NON-WOVEN GAUZE PADS, WITHOUT X-RAY DETECTABLE THREAD, STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark 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

wound compress by Danyang Sunmed Healthcare Corporation — Class I — CE/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
CN-MF-000013734
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED ea288f8e-591a-4858-ac49-5291dc003a95 61 fields · synced Oct 7, 2026