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Iga

EUDAMED

Class B (EU MDR)

Ref 1418-0787Ref 1419-0780

by Medicon Hellas SA

Identity

Trade Name
IGA EUDAMED
Device Name
IGA EUDAMED
Model / Reference
1418-0787 EUDAMED
1419-0780 EUDAMED

Identifiers

Primary DI / UDI-DI
05204309071050 EUDAMED
05204309123100 EUDAMED
Basic UDI-DI
5204309000028NY EUDAMED
EMDN Code
W0102010101 IMMUNOGLOBULIN A EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Greece EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Iga by Medicon Hellas SA — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Medicon Hellas SA
EUDAMED SRN
GR-MF-000013625

Sources (2)

  • EUDAMED 3c47dacd-190e-4f5b-9715-7bf366dfc01f 61 fields · synced Jul 15, 2026
  • EUDAMED 840ea019-a749-4e42-9021-81e2b601f1a9 61 fields · synced May 18, 2026