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Respireo Primo P Non Vented

EUDAMED

Class IIa (EU MDR)

Ref 472106

by Air Liquide Medical Systems S.r.l.

Identity

Trade Name
Respireo Primo P Non Vented EUDAMED
Device Name
Respireo Primo P Non Vented EUDAMED
Model / Reference
472106 EUDAMED

Identifiers

Primary DI / UDI-DI
08015662721066 EUDAMED
Basic UDI-DI
8015662RESPPRIMOPNVES 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 P 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 5b2b00fa-f650-42cd-84f7-d12da3e547f4 61 fields · synced Jul 8, 2026