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Ureterorenoscope

EUDAMED

Class IIa (EU MDR)

Ref 30-0639-60Model Ureterorenoscope

by Innoview GmbH

Identity

Trade Name
Ureterorenoscope EUDAMED
Device Name
Rigid Endoscope EUDAMED
Model / Reference
Ureterorenoscope EUDAMED
30-0639-60 EUDAMED

Identifiers

Primary DI / UDI-DI
+EINV300639601Q 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

Category: Flexible video ureteroscope, single-use

Ureterorenoscope by Innoview GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video ureteroscope, single-use.

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 30e435b8-69a3-4cdf-a77b-ca9b96d7c488 61 fields · synced Jun 19, 2026