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Lactate

by Medicon Hellas SA

Ref 1517-1090

Lactate (1517-1090) is a Class C device made by Medicon Hellas SA, registered in EUDAMED on 17 Sep 2026 (Basic UDI-DI 5204309000085PC), active as of 23 Oct 2026.

Active European Union

CE IVDR

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number5204309000085PC Basic UDI-DI 05204309175680UDI-DIDate17 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Model / reference
1517-1090
Primary DI / UDI-DI
05204309175680
Basic UDI-DI
5204309000085PC
EMDN code
W01010218 Lactate
Device class
Class C
EU registration type
Standard device
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000013625

Similar devices in this category

Other devices filed under LACTATE.

Other devices from Medicon Hellas SA

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Properties

  • Contains substances of microbial origin
  • Reagent
  • IVD kit
  • Professional testing
Other properties (9, all answered No)