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VersaVue™ Single-Use Flexible Cystoscope (Reverse, box)

EUDAMED

Class IIa (EU MDR)

Ref M0067801500Model EUC 100

by Medimaging Integrated Solution Inc

Identity

Trade Name
VersaVue™ Single-Use Flexible Cystoscope (Reverse, box) EUDAMED
Device Name
VersaVue™ Single-Use Flexible Cystoscope EUDAMED
Model / Reference
EUC 100 EUDAMED
M0067801500 EUDAMED

Identifiers

Primary DI / UDI-DI
04719872715139 EUDAMED
Basic UDI-DI
47198727150018R EUDAMED
Direct Marketing DI
04719872715139 EUDAMED
EMDN Code
Z12020701 CYSTOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands 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

VersaVue™ Single-Use Flexible Cystoscope (Reverse, box) by Medimaging Integrated Solution Inc. — Class IIa — MDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
TW-MF-000009317
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 09f72abd-55a4-45b1-895a-6893b24c6b21 61 fields · synced Jun 19, 2026