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Seesheen

EUDAMED

Class IIa (EU MDR)

Ref EG-GP13TModel EG-GP13N、EG-GP13N pro、EG-GP13、EG-GP13 pro、EG-GP13T、EG-GP13T pro、EG-GP13J、EG-GP13Jpro、EG-GP13BJ、EG-GP13BJ pro

by Zhuhai Seesheen Medical Technology Co., Ltd.

Identity

Trade Name
SEESHEEN EUDAMED
Device Name
Video Gastroscope EUDAMED
Model / Reference
EG-GP13N、EG-GP13N pro、EG-GP13、EG-GP13 pro、EG-GP13T、EG-GP13T pro、EG-GP13J、EG-GP13Jpro、EG-GP13BJ、EG-GP13BJ pro EUDAMED
EG-GP13T EUDAMED

Identifiers

Primary DI / UDI-DI
06970680130523 EUDAMED
Basic UDI-DI
69706801326EGB4 EUDAMED
Direct Marketing DI
06970680130523 EUDAMED
EMDN Code
Z12020511 VIDEO GASTROSCOPES 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

Seesheen by Zhuhai Seesheen 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-000027274
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 177d0473-f199-435a-be1a-aa65880ccd8f 61 fields · synced Jun 18, 2026