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Seesheen

EUDAMED

Class I (EU MDR)

Ref BR-15AP plusModel BR-15AF、BR-15AF plus、BR-15AP、BR-15AP plus、BR-15A、BR-15A plus

by Zhuhai Seesheen Medical Technology Co., Ltd.

Identity

Trade Name
SEESHEEN EUDAMED
Device Name
Flexible Video Bronchoscope EUDAMED
Model / Reference
BR-15AF、BR-15AF plus、BR-15AP、BR-15AP plus、BR-15A、BR-15A plus EUDAMED
BR-15AP plus EUDAMED

Identifiers

Primary DI / UDI-DI
06970680131995 EUDAMED
Basic UDI-DI
69706801339BRC7 EUDAMED
Direct Marketing DI
06970680131995 EUDAMED
EMDN Code
Z12020802 VIDEO BRONCHOSCOPES EUDAMED

Classification

Device Class
Class I 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 I — CE/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 de4a844b-2a0b-4191-b2c2-8417a3a23466 61 fields · synced Oct 7, 2026