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Hysteroscope

EUDAMED

Class IIa (EU MDR)

Ref J1330ETModel XG-5/XG-5A/ZG-1

by Shenyang Shenda Endoscope Co., Ltd.

Identity

Device Name
Hysteroscope EUDAMED
Model / Reference
XG-5/XG-5A/ZG-1 EUDAMED
J1330ET EUDAMED

Identifiers

Primary DI / UDI-DI
06971244213461 EUDAMED
Basic UDI-DI
697124421GQJ0001CH EUDAMED
EMDN Code
Z12020704 HYSTEROSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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: Rigid video hysteroscope

Hysteroscope by Shenyang Shenda Endoscope Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Rigid video hysteroscope.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000030478
Authorised Representative
Lepu Medical (Europe) Cooperatief U.A. NL-AR-000000551

Sources (1)

  • EUDAMED db1977ab-9026-4020-bd60-9f881887efc2 61 fields · synced Jun 18, 2026