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Rinoflow

EUDAMED

Class IIa (EU MDR)

Ref 408000

by Air Liquide Medical Systems S.r.l.

Identity

Trade Name
Rinoflow EUDAMED
Device Name
Rinoflow EUDAMED
Model / Reference
408000 EUDAMED

Identifiers

Primary DI / UDI-DI
08015662080002 EUDAMED
Basic UDI-DI
8015662RINOFLOWBV EUDAMED
EMDN Code
Z12159002 AEROSOL EQUIPMENT 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Rinoflow 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 aa173ee2-2789-44d8-87f3-726b26943c95 61 fields · synced Jun 18, 2026