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Single-Use Flexible Video Bronchoscope

EUDAMED

Class IIa (EU MDR)

Ref G11003

by Transmed (China) Co., Ltd.

Identity

Device Name
Single-Use Flexible Video Bronchoscope EUDAMED
Model / Reference
G11003 EUDAMED

Identifiers

Primary DI / UDI-DI
06932619743105 EUDAMED
Basic UDI-DI
69326197DC609639V EUDAMED
EMDN Code
Z12020802 VIDEO BRONCHOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

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

Single-Use Flexible Video Bronchoscope by Transmed (china) 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-000029614
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 48ecd732-f0ab-4a84-b959-9d5526f2e2da 61 fields · synced Jul 19, 2026