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Ventea S

EUDAMED

Class IIa (EU MDR)

Ref M-117023

by Sefam

Identity

Trade Name
Ventea S EUDAMED
Device Name
Néa Duo EUDAMED
Model / Reference
M-117023 EUDAMED

Identifiers

Primary DI / UDI-DI
03700659401186 EUDAMED
Basic UDI-DI
3700659417029A EUDAMED
EMDN Code
Z12030103 PULMONARY VENTILATORS FOR NON–HOSPITAL USE EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

No

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

Ventea S by Sefam — 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

Manufacturer
Sefam
EUDAMED SRN
FR-MF-000009061

Sources (1)

  • EUDAMED 0592fb99-1d1a-44cc-adc2-7735215f566a 61 fields · synced Jun 19, 2026