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Medication Cup

EUDAMED

Class IIa (EU MDR)

Ref MAproX-TModel MAPro5N

by Feellife Health Inc.

Identity

Device Name
Medication Cup EUDAMED
Model / Reference
MAPro5N EUDAMED
MAproX-T EUDAMED

Identifiers

Primary DI / UDI-DI
06934325308425 EUDAMED
Basic UDI-DI
69343253R0680Y15FFU EUDAMED
Direct Marketing DI
06934325308425 EUDAMED
EMDN Code
R0680 NEBULISATION AND HUMIDIFICATION SYSTEMS - ACCESSORIES NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

Medication Cup 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 (1)

  • EUDAMED 80845fa0-59b5-4e2b-8da0-4e0f13e64a7d 61 fields · synced Jun 19, 2026