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Single-use Flexible Uretero-Renoscope

EUDAMED

Class IIa (EU MDR)

Ref DUC-M20Model DUC-M10, DUC-M20, DUC-M30, DUC-N10, DUC-N30

by Zhuhai Vision Medical Technology Co., Ltd

Identity

Device Name
Single-use Flexible Uretero-Renoscope EUDAMED
Model / Reference
DUC-M10, DUC-M20, DUC-M30, DUC-N10, DUC-N30 EUDAMED
DUC-M20 EUDAMED

Identifiers

Primary DI / UDI-DI
06971558931396 EUDAMED
Basic UDI-DI
697155893DUCV6 EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Category: Flexible video ureteroscope, single-use

Single-use Flexible Uretero-Renoscope by Zhuhai Vision Medical Technology Co., Ltd — 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
Zhuhai Vision Medical Technology Co., Ltd
EUDAMED SRN
CN-MF-000016785
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED cf8a7660-5796-400c-ad79-6fc90db49eeb 61 fields · synced Jun 18, 2026