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Haptoglobin

by Medicon Hellas SA 2 variants

Ref 1418-0846

Haptoglobin (1418-0846) is a device classified as IVD General made by Medicon Hellas SA, registered in EUDAMED on 13 Dec 2023 (Basic UDI-DI B-05204309085415), active as of 24 Oct 2026.

Active European Union

CE IVDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-05204309085415 Basic UDI-DI 05204309085415UDI-DIDate13 Dec 2023RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Active

Specification

EUDAMED

Model / reference
1418-0846
Primary DI / UDI-DI
05204309085415
Basic UDI-DI
B-05204309085415
EMDN code
W0102010302 Haptoglobin
Device class
Class IVD General
EU registration type
Legacy device (under a directive)
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000013625

Similar devices in this category

Other devices filed under HAPTOGLOBIN.

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 (8, all answered No)