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Tritube®

EUDAMED

Class IIa (EU MDR)

Ref 7000

by International Emergency Services, S.L. (IES MEDICAL®)

Identity

Trade Name
Tritube® EUDAMED
Device Name
Tritube EUDAMED
Model / Reference
7000 EUDAMED

Identifiers

Primary DI / UDI-DI
08437025198429 EUDAMED
Basic UDI-DI
8437025198TrachealTubesV7 EUDAMED
EMDN Code
R01030201 ENDOTRACHEAL TUBES, CUFFED, NOT REINFORCED EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain 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

Tritube® by International Emergency Services, S.L. (IES MEDICAL®) — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
ES-MF-000045282

Sources (1)

  • EUDAMED 0293c4df-caba-402c-ae26-60fb9bfaf811 61 fields · synced Oct 6, 2026