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Seesheen

EUDAMED

Class IIa (EU MDR)

Ref CY-1356

by Zhuhai Seesheen Medical Technology Co., Ltd.

Identity

Trade Name
Seesheen EUDAMED
Device Name
Flexible video cystonephroscope EUDAMED
Model / Reference
CY-1356 EUDAMED

Identifiers

Primary DI / UDI-DI
06970680130301 EUDAMED
Basic UDI-DI
B-06970680130301 EUDAMED
EMDN Code
Z12020711 VIDEO CYSTOURETHROSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Seesheen by Zhuhai Seesheen Medical Technology Co., Ltd. — Class IIa — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000027274
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED d25faa3f-92c1-4947-af31-4f4ebe2b415d 61 fields · synced Oct 7, 2026