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Aposan

EUDAMED

Class IIa (EU MDR)

Ref MApro2Model MA8Ref Air Pro Ⅲ

by Feellife Health Inc.

Identity

Trade Name
Aposan EUDAMED
APOSAN Portable Mesh Nebulizer EUDAMED
Device Name
Medication Cup EUDAMED
Portable Mesh Nebulizer EUDAMED
Model / Reference
MA8 EUDAMED
MApro2 EUDAMED
Air Pro Ⅲ EUDAMED

Identifiers

Primary DI / UDI-DI
06934325310053 EUDAMED
06934325309507 EUDAMED
Basic UDI-DI
69343253R068012AY9P EUDAMED
69343253R06010115C8E EUDAMED
Direct Marketing DI
06934325309507 EUDAMED
EMDN Code
R0680 NEBULISATION AND HUMIDIFICATION SYSTEMS - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED
R060101 COLD NEBULISATION SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
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

EUDAMEDEUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Aposan by Feellife Health Inc. — 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
CN-MF-000000782
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED 86cd8843-9943-4e0c-ac6e-9c1babd6678c 61 fields · synced Jul 21, 2026
  • EUDAMED 6e004e3f-b7b1-42fc-992b-c34dafd35ac2 61 fields · synced May 18, 2026