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Flexible Video Ureterorenoscope

EUDAMED

Class IIa (EU MDR)

Ref UR-332Model UR-332, UR-328

by Zhuhai Seesheen Medical Technology Co., Ltd.

Identity

Device Name
Flexible Video Ureterorenoscope EUDAMED
Model / Reference
UR-332, UR-328 EUDAMED
UR-332 EUDAMED

Identifiers

Primary DI / UDI-DI
06970680130646 EUDAMED
Basic UDI-DI
69706801310URC5 EUDAMED
Direct Marketing DI
06970680130646 EUDAMED
EMDN Code
Z12020713 URETERORENOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

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

Flexible Video Ureterorenoscope by Zhuhai Seesheen 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 Seesheen Medical Technology Co., Ltd.
EUDAMED SRN
CN-MF-000027274
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 7883fefe-57a4-44d2-ac39-5a7665525e0c 61 fields · synced Jun 18, 2026