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feellife

EUDAMED

Class IIa (EU MDR)

Ref Air Pro IXModel Air Pro VIII

by Feellife Health Inc.

Identity

Trade Name
feellife EUDAMED
Model / Reference
Air Pro VIII EUDAMED
Air Pro IX EUDAMED

Identifiers

Primary DI / UDI-DI
06934325303598 EUDAMED
Basic UDI-DI
B-06934325303598 EUDAMED
EMDN Code
R060101 COLD NEBULISATION SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

feellife by Feellife Health Inc. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000000782
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 348d21e1-5701-4fc1-8e4a-9342b99e79d9 61 fields · synced May 23, 2026