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Uromed Nephro-Kath

EUDAMED

Class IIb (EU MDR)

Ref 2525.10

by UROMED Kurt Drews KG

Identity

Trade Name
UROMED NEPHRO-KATH EUDAMED
Device Name
NC01 EUDAMED
Model / Reference
2525.10 EUDAMED

Identifiers

Primary DI / UDI-DI
04250098803557 EUDAMED
Basic UDI-DI
B-04250098803557 EUDAMED
EMDN Code
U040203 NEPHROSTOMY CATHETERS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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 Nephro-Kath by UROMED Kurt Drews KG — Class IIb — 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

EUDAMED SRN
DE-MF-000006084

Sources (1)

  • EUDAMED 2c7976ff-1760-4db4-87a1-1b19d40d808f 61 fields · synced Jun 18, 2026