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Single-use Flexible Cystoscope

EUDAMED

Class IIa (EU MDR)

Ref DCC-U10Model DCC-U10,DCC-U30,DCC-W10,DCC-W30

by Zhuhai Vision Medical Technology Co., Ltd

Identity

Device Name
Single-use Flexible Cystoscope EUDAMED
Model / Reference
DCC-U10,DCC-U30,DCC-W10,DCC-W30 EUDAMED
DCC-U10 EUDAMED

Identifiers

Primary DI / UDI-DI
06971558931341 EUDAMED
Basic UDI-DI
697155893DCCTG EUDAMED
EMDN Code
Z12020701 CYSTOSCOPES 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

Single-use Flexible Cystoscope by Zhuhai Vision Medical Technology 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-000016785
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 4ffb21ba-2e44-4367-a224-4c2829bfd395 61 fields · synced Jun 18, 2026