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Laryngectomy tube, cuffed

EUDAMED

Class IIa (EU MDR)

Ref 121161-000110

by Teleflex Medical

Identity

Trade Name
Laryngectomy tube, cuffed EUDAMED
Device Name
RÜSCH Laryngoflex EUDAMED
Model / Reference
121161-000110 EUDAMED

Identifiers

Primary DI / UDI-DI
14026704761743 EUDAMED
Basic UDI-DI
08019020000000000000177KY EUDAMED
EMDN Code
R01030202 ENDOTRACHEAL TUBES, CUFFED, REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Ireland 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

Category: Reinforced endotracheal tube, single-use

Laryngectomy tube, cuffed by Teleflex Medical — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Reinforced endotracheal tube, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Teleflex Medical
EUDAMED SRN
IE-MF-000015868

Sources (1)

  • EUDAMED 7d68a423-e93a-4f48-9bb2-e7db672c132a 61 fields · synced Jun 18, 2026