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Ampolla Rinoflow

EUDAMED

Class IIa (EU MDR)

Ref 471082

by Air Liquide Medical Systems S.r.l.

Identity

Trade Name
Ampolla Rinoflow EUDAMED
Device Name
Ampolla Rinoflow EUDAMED
Model / Reference
471082 EUDAMED

Identifiers

Primary DI / UDI-DI
08015662710824 EUDAMED
Basic UDI-DI
8015662AMPRINOFLOWUH EUDAMED
EMDN Code
R03010380 AEROSOL THERAPY SYSTEMS - ACCESSORIES 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

Ampolla 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 ae88da34-1830-4972-823d-539b4c2fc024 61 fields · synced Jun 18, 2026