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Endobronchial Tube

EUDAMED

Class IIa (EU MDR)

Ref 91070008Model Right:32Fr

by Guangzhou Orcl Medical Co., Ltd.

Identity

Trade Name
Endobronchial Tube EUDAMED
Device Name
Endobronchial Tube EUDAMED
Model / Reference
Right:32Fr EUDAMED
91070008 EUDAMED

Identifiers

Primary DI / UDI-DI
06972745360678 EUDAMED
Basic UDI-DI
B-06972745360678 EUDAMED
EMDN Code
R01040199 ENDOBRONCHIAL TUBES, RIGHT - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Endobronchial Tube by Guangzhou Orcl Medical Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000039222
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED 242fa777-830e-4b32-98b8-977fe9d985ca 61 fields · synced Jun 18, 2026