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Airflow Plus

by E.M.S. Electro Medical Systems S.A. 3 variants

Ref DV-082/X

Airflow Plus (DV-082/X) is a Class IIa device made by E.M.S. Electro Medical Systems S.A., registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI 07613353020KU), active as of 7 Nov 2026.

Active European Union

CE MDR

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/MDR Number07613353020KU Basic UDI-DI 07613353341152UDI-DIDate3 Nov 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
AIRFLOW Powders
Model / reference
DV-082/X
Primary DI / UDI-DI
07613353341152
Basic UDI-DI
07613353020KU
Direct marketing DI
07613353341169
EMDN code
Q01010403 Dental abrasive and polishing materials
Device class
Class IIa
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000026136
Authorised representative
EMS FRANCE SARL FR-AR-000011266

Similar devices in this category

Other devices filed under DENTAL ABRASIVE AND POLISHING MATERIALS.

Other devices from E.M.S. Electro Medical Systems S.A.

See all devices from E.M.S. Electro Medical Systems S.A. →

Properties

Other properties (14, all answered No)