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Compressor Nebulizer

EUDAMED

Class IIa (EU MDR)

Ref A500LW07

by Shenzhen Aeon Technology Co., Ltd.

Identity

Trade Name
Compressor Nebulizer EUDAMED
Device Name
Compressor Nebulizer EUDAMED
Model / Reference
A500LW07 EUDAMED

Identifiers

Primary DI / UDI-DI
06947832500220 EUDAMED
Basic UDI-DI
B-06947832500220 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

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 — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000012690
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED a0bcc209-37b4-4d30-a75f-641606c59d1a 61 fields · synced Jun 19, 2026