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Respireo Primo F

EUDAMED

Class IIa (EU MDR)

Ref 472531

by Air Liquide Medical Systems S.r.l.

Identity

Trade Name
Respireo Primo F EUDAMED
Device Name
Respireo Primo F EUDAMED
Model / Reference
472531 EUDAMED

Identifiers

Primary DI / UDI-DI
08015662725316 EUDAMED
Basic UDI-DI
8015662RESPPRIMOFKU EUDAMED
EMDN Code
R0301010201 CPAP 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

Respireo Primo F by Air Liquide Medical Systems S.r.l. — 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
IT-MF-000015627

Sources (1)

  • EUDAMED d60b495c-7ee8-464c-9e4c-4a2971100492 61 fields · synced Jun 19, 2026