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Catheter Spigot

EUDAMED

Class I (EU MDR)

Ref 20360

by Curas Sdn. Bhd.

Identity

Device Name
Catheter Spigot EUDAMED
Model / Reference
20360 EUDAMED

Identifiers

Primary DI / UDI-DI
05051400203602 EUDAMED
Basic UDI-DI
B-05051400203602 EUDAMED
EMDN Code
U0180 URETHRAL PROSTATIC AND BLADDER CATHETERS - ACCESSORIES 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Catheter Spigot by Curas Sdn. Bhd. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Curas Sdn. Bhd.
EUDAMED SRN
MY-MF-000036883
Authorised Representative
Kabomed GmbH AT-AR-000007569

Sources (1)

  • EUDAMED 99e26c6b-8b81-44e7-b70c-9b2f4b69a234 61 fields · synced Jul 17, 2026