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Tracheostomy Tube

EUDAMED

Class IIa (EU MDR)

Ref 91100015Model Cuffed:10.0#

by Guangzhou Orcl Medical Co., Ltd.

Identity

Trade Name
Tracheostomy Tube EUDAMED
Device Name
Tracheostomy Tube EUDAMED
Model / Reference
Cuffed:10.0# EUDAMED
91100015 EUDAMED

Identifiers

Primary DI / UDI-DI
06972745363273 EUDAMED
Basic UDI-DI
B-06972745363273 EUDAMED
EMDN Code
R0105020101 TRACHEOSTOMIC CANNULAS, CUFFED, NOT REINFORCED, WITH FIXED FLANGE, AND KITS 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

No

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

Category: Tracheostomy tube, non-reinforced, non-customized, single-use

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

Similar devices

Also classified as Tracheostomy tube, non-reinforced, non-customized, single-use.

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 1bc5c7a9-0013-4414-b39f-48ee7c3c2045 61 fields · synced Oct 6, 2026