Atomisor Aerosonic+

by La Diffusion Technique Française

Ref AOHBOX+Model ATOMISOR AEROSONIC+

Active European Union

CE MDR CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	Number3664351AAECL-AAESOG3 Basic UDI-DI 36643511001538UDI-DI	Date19 Dec 2025Registered	StatusActive
European Union	CE/MDR	Number3664351AAECL-AAESOG3 Basic UDI-DI 36643511001538UDI-DI	Date19 Dec 2025Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device Name: Classic and Sonic Aerosol Compressor
Sonic Aerosol Compressor
Model / Reference: AOHBOX+, ATOMISOR AEROSONIC+

Primary DI / UDI-DI: 36643511001538
Basic UDI-DI: 3664351AAECL-AAESOG3, B-36643511001538
EMDN Code: Z12159002 Aerosol equipment

Device Class: Class IIa
EU market of registration: France

Manufacturer details

EUDAMED SRN: FR-MF-000009060

Other devices from La Diffusion Technique Française

Pureneb Aerosonic+

Class IIa

Properties

Administering Medicine

Other properties (12)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Measuring Function: No
Incorporates Medicinal Product: No