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Video Cystoscope

EUDAMED

Class IIa (EU MDR)

Ref /Model VC-2900HQ

by HUGER Medical Instrument Co., Ltd.

Identity

Device Name
Video Cystoscope EUDAMED
Model / Reference
VC-2900HQ EUDAMED
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06953393115032 EUDAMED
Basic UDI-DI
69533931CY29QQC EUDAMED
EMDN Code
Z12020701 CYSTOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Video Cystoscope by HUGER Medical Instrument Co., Ltd. — 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

EUDAMED SRN
CN-MF-000001128
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 381f4244-fa36-4a78-9f86-4402be25ffa1 61 fields · synced Jul 16, 2026