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Single use flexible bronchoscope

EUDAMED

Class IIa (EU MDR)

Ref BR-D3Model BR-D1,BR-D2,BR-D3,BR-D4,BR-F1,BR-F2,BR-F3,BR-F4

by Shenzhen Besdata Technology Co., Ltd

Identity

Trade Name
Single use flexible bronchoscope EUDAMED
Device Name
Single use flexible bronchoscope EUDAMED
Model / Reference
BR-D1,BR-D2,BR-D3,BR-D4,BR-F1,BR-F2,BR-F3,BR-F4 EUDAMED
BR-D3 EUDAMED

Identifiers

Primary DI / UDI-DI
06971355350734 EUDAMED
Basic UDI-DI
69713553501928Q EUDAMED
EMDN Code
Z12020801 BRONCHOSCOPES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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 bronchoscope by Shenzhen Besdata Technology 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-000018921
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED cd8b3511-1941-4cea-8d6f-ee39c8683c71 61 fields · synced Jun 18, 2026