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ApWell Silent Mesh

EUDAMED

Class IIa (EU MDR)

Ref AeroCentre+ Model AeroCentre+

by Feellife Health Inc.

Identity

Trade Name
ApWell Silent Mesh EUDAMED
Device Name
Portable Mesh Nebulizer EUDAMED
Model / Reference
AeroCentre+ EUDAMED

Identifiers

Primary DI / UDI-DI
06934325311562 EUDAMED
Basic UDI-DI
69343253R06010121C87 EUDAMED
Direct Marketing DI
06934325311562 EUDAMED
EMDN Code
R060101 COLD NEBULISATION SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Croatia 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

ApWell Silent Mesh 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 1249457d-aa87-454e-ab02-8ae5863972ae 61 fields · synced Jun 18, 2026