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UROMED SIMPLYCATH mobil Trial Set »male«

EUDAMED

Class I (EU MDR)

Ref 3605.12Ref 3605.16

by UROMED Kurt Drews KG

Identity

Trade Name
UROMED SIMPLYCATH mobil Trial Set »male« EUDAMED
Device Name
ISC01 EUDAMED
Model / Reference
3605.12 EUDAMED
3605.16 EUDAMED

Identifiers

Primary DI / UDI-DI
04250098835763 EUDAMED
04250098835787 EUDAMED
Basic UDI-DI
04250098810019EP 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

UROMED SIMPLYCATH mobil Trial Set »male« by UROMED Kurt Drews KG — 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
DE-MF-000006084

Sources (2)

  • EUDAMED 857980cc-a18b-4d9f-8dae-65490a4a31ff 61 fields · synced Oct 6, 2026
  • EUDAMED d084bc80-103a-4fe5-8afa-7f45b1f6186e 61 fields · synced May 18, 2026