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Kompresa

EUDAMED

Class I (EU MDR)

Ref 5*5cm

by Danyang Sunmed Healthcare Corporation

Identity

Trade Name
Kompresa EUDAMED
Device Name
Non-woven swab EUDAMED
Model / Reference
5*5cm EUDAMED

Identifiers

Primary DI / UDI-DI
06974567463537 EUDAMED
Basic UDI-DI
6974567460001363 EUDAMED
Direct Marketing DI
06974567463537 EUDAMED
EMDN Code
M0202030101 NON-WOVEN GAUZE PADS, WITHOUT X-RAY DETECTABLE THREAD, STERILE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Slovenia 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

Kompresa by Danyang Sunmed Healthcare Corporation — 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
CN-MF-000013734
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 748cc15f-5a8e-49db-9031-a93dbb6e791e 61 fields · synced Oct 6, 2026