← Back to catalogue

Reinforced Endotracheal Tubes with Cuff

EUDAMED

Class IIa (EU MDR)

Ref 20430Model Endotracheal Tube with/ without Cuffed with/ without reinforced

by Poly Medicure Limited

Identity

Trade Name
Reinforced Endotracheal Tubes with Cuff EUDAMED
Device Name
Endotracheal Tube with/ without Cuffed with/ without reinforced EUDAMED
Model / Reference
Endotracheal Tube with/ without Cuffed with/ without reinforced EUDAMED
20430 EUDAMED

Identifiers

Primary DI / UDI-DI
08902095204306 EUDAMED
Basic UDI-DI
890209520153E3 EUDAMED
EMDN Code
R01030202 ENDOTRACHEAL TUBES, CUFFED, REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Reinforced endotracheal tube, single-use

Reinforced Endotracheal Tubes with Cuff by Poly Medicure Limited — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
IN-MF-000043011
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 66b58279-22a0-4d30-90c2-94ee02f39694 61 fields · synced Aug 2, 2026