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Newsept Plus

by Demo S.A. Pharmaceutical Industry

Ref Newsept Plus

Newsept Plus is a Class IIb device made by Demo S.A. Pharmaceutical Industry, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI B-05205411014607), 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-05205411014607 Basic UDI-DI Date26 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Newsept Plus
Model / reference
Newsept Plus
Primary DI / UDI-DI
05205411014607, 05205411014591
Basic UDI-DI
B-05205411014607, B-05205411014591
EMDN code
Q02030204 Contact lenses storing and cleaning solutions
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000023096

Similar devices in this category

Other devices filed under OPHTHALMOLOGY, LIQUID FLUIDS.

Other devices from Demo S.A. Pharmaceutical Industry

Properties

  • Supplied sterile
Other properties (11, all answered No)