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Compressor Nebulizer

EUDAMED

Class IIa (EU MDR)

Ref A500LWD02Model A500LWD01, A500LWD02, A500LWD04, A500LWD05, A500LWDC01, A500LWDC02, A500LWDC04, A500LWDC05

by Shenzhen Aeon Technology Co., Ltd.

Identity

Trade Name
Compressor Nebulizer EUDAMED
Device Name
Compressor Nebulizer EUDAMED
Model / Reference
A500LWD01, A500LWD02, A500LWD04, A500LWD05, A500LWDC01, A500LWDC02, A500LWDC04, A500LWDC05 EUDAMED
A500LWD02 EUDAMED

Identifiers

Primary DI / UDI-DI
06947832500268 EUDAMED
Basic UDI-DI
69478325CNDX2024010800WZ EUDAMED
Direct Marketing DI
06947832500268 EUDAMED
EMDN Code
Z12159002 AEROSOL EQUIPMENT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Poland 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

Compressor Nebulizer by Shenzhen Aeon Technology Co., Ltd. — 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-000012690
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 55f82437-43a4-452f-9196-674c2ae84e3b 61 fields · synced Jun 18, 2026