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Respireo Primo N Non Vented

EUDAMED

Class IIa (EU MDR)

Ref 472350

by Air Liquide Medical Systems S.r.l.

Identity

Trade Name
Respireo Primo N Non Vented EUDAMED
Device Name
Respireo Primo N Non Vented EUDAMED
Model / Reference
472350 EUDAMED

Identifiers

Primary DI / UDI-DI
08015662723503 EUDAMED
Basic UDI-DI
8015662RESPPRIMONNVEG EUDAMED
EMDN Code
R0301010202 NIV MASKS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Category: Rebreathing oxygen face mask

Respireo Primo N Non Vented by Air Liquide Medical Systems S.r.l. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Rebreathing oxygen face mask.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IT-MF-000015627

Sources (1)

  • EUDAMED 9ed1bcb9-3763-4329-b448-ad33ec8be45a 61 fields · synced Jun 18, 2026