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4K 3D Video Endoscope

EUDAMED

Class IIa (EU MDR)

Ref M 31030AModel M 31030A, M 31000A, M 31030PA, M 31000PA, G 31030A, G 31000A, G 31030PA, G 31000PA

by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Identity

Device Name
4K 3D Video Endoscope EUDAMED
Model / Reference
M 31030A, M 31000A, M 31030PA, M 31000PA, G 31030A, G 31000A, G 31030PA, G 31000PA EUDAMED
M 31030A EUDAMED

Identifiers

Primary DI / UDI-DI
06903053050951 EUDAMED
Basic UDI-DI
69449040AB065100068B EUDAMED
Direct Marketing DI
06903053050951 EUDAMED
EMDN Code
Z12029099 VARIOUS INSTRUMENTS FOR ENDOSCOPY AND MINI–INVASIVE SURGERY – OTHER 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

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

4K 3D Video Endoscope by Shenzhen Mindray Bio-Medical Electronics 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-000014156
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 4fd196a3-34d1-4f26-9ac7-8f5831fedb2e 61 fields · synced Jun 18, 2026