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Ureterorenoscope

EUDAMED

Class IIa (EU MDR)

Ref 30-0514-02Model Ureterorenoscope

by Innoview GmbH

Identity

Trade Name
Ureterorenoscope EUDAMED
Device Name
Rigid Endoscope EUDAMED
Model / Reference
Ureterorenoscope EUDAMED
30-0514-02 EUDAMED

Identifiers

Primary DI / UDI-DI
+EINV300514021E EUDAMED
Basic UDI-DI
++EINV30037112FL EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Ureterorenoscope by Innoview GmbH — Class IIa — 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

Manufacturer
Innoview GmbH
EUDAMED SRN
DE-MF-000005567

Sources (1)

  • EUDAMED a86e75ee-9ecc-4e12-b025-3767bb3d7e7d 61 fields · synced Jun 19, 2026