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feellife

EUDAMED

Class IIa (EU MDR)

Ref Air Pro IXRef Air Pro IX Model Air Pro Ⅸ

by Feellife Health Inc.

Identity

Trade Name
feellife EUDAMED
Device Name
Portable Mesh Nebulizer EUDAMED
Model / Reference
Air Pro IX EUDAMED
Air Pro Ⅸ EUDAMED

Identifiers

Primary DI / UDI-DI
06934325304861 EUDAMED
Basic UDI-DI
B-06934325304861 EUDAMED
69343253R06010126A8J EUDAMED
Direct Marketing DI
06934325304861 EUDAMED
EMDN Code
R060101 COLD NEBULISATION SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED
Spain 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

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

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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 (2)

  • EUDAMED 6a49a82f-14ea-4b73-99d6-1a1f698f9667 61 fields · synced Aug 1, 2026
  • EUDAMED 149a7e90-c2da-40e7-92f1-081b646f7fc1 61 fields · synced May 17, 2026