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Seesheen

EUDAMED

Class IIa (EU MDR)

Ref UR-1331

by Zhuhai Seesheen Medical Technology Co., Ltd.

Identity

Trade Name
Seesheen EUDAMED
Device Name
Flexible video ureterorenoscope EUDAMED
Model / Reference
UR-1331 EUDAMED

Identifiers

Primary DI / UDI-DI
06970680130165 EUDAMED
Basic UDI-DI
B-06970680130165 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Flexible video ureteroscope, single-use

Seesheen by Zhuhai Seesheen Medical Technology Co., Ltd. — Class IIa — MDD — 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/MDD

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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 2b20eaf8-2385-4a67-a3a3-aea5f9e4207a 61 fields · synced Jun 18, 2026