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Seesheen

EUDAMED

Class I (EU MDR)

Ref EN-E19HModel EN-E19H,EN-1029,EN-1039

by Zhuhai Seesheen Medical Technology Co., Ltd.

Identity

Trade Name
SEESHEEN EUDAMED
Device Name
Flexible video rhinolaryngoscope EUDAMED
Model / Reference
EN-E19H,EN-1029,EN-1039 EUDAMED
EN-E19H EUDAMED

Identifiers

Primary DI / UDI-DI
06970680130387 EUDAMED
Basic UDI-DI
69706801308ENBE EUDAMED
Direct Marketing DI
06970680130387 EUDAMED
EMDN Code
Z12021006 VIDEO NASOPHARYNGO/LARYNGOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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 I — 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 bf88d66b-b921-462f-8387-96d05770e737 61 fields · synced Oct 5, 2026