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Urea

EUDAMED

Class B (EU MDR)

Ref 1516-0020

by Medicon Hellas SA

Identity

Trade Name
UREA EUDAMED
Device Name
UREA EUDAMED
Model / Reference
1516-0020 EUDAMED

Identifiers

Primary DI / UDI-DI
05204309175246 EUDAMED
Basic UDI-DI
5204309000046P2 EUDAMED
EMDN Code
W01010204 UREA/BLOOD UREA NITROGEN 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

Urea 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 aa9cbc5f-8226-4dfc-a568-c98394f3d25c 61 fields · synced May 23, 2026