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Mobile Flexible video bronchoscope

EUDAMED

Class IIa (EU MDR)

Ref AF-2042Model AF-2028, AF-2031, AF-2042, AF-2049,AF-2052,AF-2055,AF-2058

by Zhuhai Seesheen Medical Technology Co., Ltd.

Identity

Device Name
Mobile Flexible video bronchoscope EUDAMED
Model / Reference
AF-2028, AF-2031, AF-2042, AF-2049,AF-2052,AF-2055,AF-2058 EUDAMED
AF-2042 EUDAMED

Identifiers

Primary DI / UDI-DI
06970680130424 EUDAMED
Basic UDI-DI
69706801309AFAP EUDAMED
Direct Marketing DI
06970680130424 EUDAMED
EMDN Code
Z12020802 VIDEO BRONCHOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Romania 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

Mobile Flexible video bronchoscope by Zhuhai Seesheen Medical Technology Co., Ltd. — Class IIa — 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 0a559f0f-5068-4e1b-a424-7d4cc8173207 61 fields · synced Oct 7, 2026