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Uromed Simplycath

EUDAMED

Class I (EU MDR)

Ref 3610.08

by UROMED Kurt Drews KG

Identity

Trade Name
UROMED SIMPLYCATH EUDAMED
Device Name
ISC02 EUDAMED
Model / Reference
3610.08 EUDAMED

Identifiers

Primary DI / UDI-DI
04250098820295 EUDAMED
Basic UDI-DI
04250098810015EF EUDAMED
EMDN Code
U01010501 NELATON CATHETERS, SELF-LUBRICATING EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Category: Intermittent urethral drainage catheter, non-antimicrobial, single-use

Uromed Simplycath by UROMED Kurt Drews KG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent urethral drainage catheter, non-antimicrobial, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000006084

Sources (1)

  • EUDAMED 0fb530df-a219-401d-81f6-2852b730211b 61 fields · synced Jun 18, 2026