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Aerosol Mask

by Hsiner Co., Ltd. 7 variants

Ref 30141

Aerosol Mask (30141) is a Class IIa device made by Hsiner Co., Ltd., registered in EUDAMED on 5 Nov 2026 (Basic UDI-DI B-04712688053228), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04712688053228 Basic UDI-DI 04712688053228UDI-DIDate5 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Aerosol Mask
Model / reference
30141
Primary DI / UDI-DI
04712688053228
Basic UDI-DI
B-04712688053228
EMDN code
R03010301 Aerosol therapy masks
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
TW-MF-000007258
Authorised representative
mdi Europa GmbH DE-AR-000006218

Similar devices in this category

Other devices filed under AEROSOL THERAPY MASKS.

Other devices from Hsiner Co., Ltd.

See all devices from Hsiner Co., Ltd. →

Properties

Other properties (12, all answered No)