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Heuer

EUDAMED

Class IIa (EU MDR)

Ref 14-240-06

by G.S.T. Corporation Limited

Identity

Trade Name
Heuer EUDAMED
Device Name
Endotracheal Tube-Plain EUDAMED
Model / Reference
14-240-06 EUDAMED

Identifiers

Primary DI / UDI-DI
89044078002372 EUDAMED
Basic UDI-DI
8904407814-240-06F8 EUDAMED
EMDN Code
R01030102 ENDOTRACHEAL TUBES, CUFFLESS, REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Bulgaria 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

Heuer by G.S.T. Corporation Limited — Class IIa — CE/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

EUDAMED SRN
IN-MF-000040767
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED ddb64d41-0d50-4bfa-b330-4230d61a1964 61 fields · synced Oct 7, 2026