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Albumin

EUDAMED

Class B (EU MDR)

Ref 1516-0190

by Medicon Hellas SA

Identity

Trade Name
ALBUMIN EUDAMED
Device Name
ALBUMIN EUDAMED
Model / Reference
1516-0190 EUDAMED

Identifiers

Primary DI / UDI-DI
05204309175369 EUDAMED
Basic UDI-DI
5204309000005NL EUDAMED
EMDN Code
W01010201 ALBUMIN (CC) EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Greece EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Albumin 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 (1)

  • EUDAMED 9fc263be-3d37-47ca-aab0-1b5274c06ce4 61 fields · synced May 23, 2026