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Ag Ett

EUDAMED

Class IIa (EU MDR)

Ref ETP70PUC1 ;ETP75PUC1; ETP80PUC1

by Hospitech Respiration Ltd.

Identity

Device Name
AG ETT EUDAMED
Model / Reference
ETP70PUC1 ;ETP75PUC1; ETP80PUC1 EUDAMED

Identifiers

Primary DI / UDI-DI
D-7290015409009VNZ EUDAMED
Basic UDI-DI
B-7290015409009VNZ EUDAMED
EMDN Code
R01030201 ENDOTRACHEAL TUBES, CUFFED, NOT 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

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: Basic endotracheal tube, single-use

Ag Ett by Hospitech Respiration Ltd — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
IL-MF-000018143
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (2)

  • EUDAMED 7681a4e0-0db9-4209-adfb-a50f7780768d 61 fields · synced Jul 10, 2026
  • EUDAMED 7681a4e0-0db9-4209-adfb-a50f7780768d-1 61 fields · synced Jun 10, 2026