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Iga

by Medicon Hellas SA 3 variants

Ref 1415-0780

Iga (1415-0780) is a Class B device made by Medicon Hellas SA, registered in EUDAMED on 19 Jun 2023 (Basic UDI-DI 5204309000028NY), 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 Number5204309000028NY Basic UDI-DI 05204309167647UDI-DIDate19 Jun 2023RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Model / reference
1415-0780
Primary DI / UDI-DI
05204309167647
Basic UDI-DI
5204309000028NY
EMDN code
W0102010101 Immunoglobulin a
Device class
Class B
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 IMMUNOGLOBULIN A.

Other devices from Medicon Hellas SA

See all devices from Medicon Hellas SA →

Properties

  • Contains animal tissues or cells
  • Reagent
  • IVD kit
  • Professional testing
Other properties (9, all answered No)