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Ferritin

EUDAMED

Class C (EU MDR)

Ref 1419-0273

by Medicon Hellas SA

Identity

Trade Name
FERRITIN EUDAMED
Device Name
FERRITIN EUDAMED
Model / Reference
1419-0273 EUDAMED

Identifiers

Primary DI / UDI-DI
05204309151011 EUDAMED
Basic UDI-DI
5204309000022NL EUDAMED
Direct Marketing DI
05204309151011 EUDAMED
EMDN Code
W0102070102 FERRITIN EUDAMED

Classification

Device Class
Class C 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

Ferritin by Medicon Hellas SA — Class C — 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 (1)

  • EUDAMED e8dffd3f-932c-4648-a573-8cf6e5f13265 61 fields · synced May 23, 2026