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UROMED HYDROPUR Ureteral Stent

EUDAMED

Class IIb (EU MDR)

Ref 4439.30

by UROMED Kurt Drews KG

Identity

Trade Name
UROMED HYDROPUR Ureteral Stent EUDAMED
Device Name
US01 EUDAMED
Model / Reference
4439.30 EUDAMED

Identifiers

Primary DI / UDI-DI
04250098845533 EUDAMED
Basic UDI-DI
04250098810057EX EUDAMED
EMDN Code
U020302 DOUBLE LOOP URETERAL STENTS 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

Sutures

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 HYDROPUR Ureteral Stent by UROMED Kurt Drews KG — Class IIb — 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 (1)

  • EUDAMED c2ee889f-326f-4e83-9787-f7d67d40dd71 61 fields · synced Jul 27, 2026