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Hekura Katheterisatie-Oefenset

EUDAMED

Class I (EU MDR)

Ref SE1000-3

by Conod Medical Co., Limited

Identity

Trade Name
HEKURA KATHETERISATIE-OEFENSET EUDAMED
Device Name
Urinary Catheterization kit EUDAMED
Model / Reference
SE1000-3 EUDAMED

Identifiers

Primary DI / UDI-DI
16955824049197 EUDAMED
Basic UDI-DI
69558240SY0200100UA0002VV EUDAMED
EMDN Code
V0599 CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

Hekura Katheterisatie-Oefenset by Conod Medical Co., Limited — 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-000012600
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED f9271989-eb90-49b7-a117-f33ef4983135 61 fields · synced Jul 9, 2026