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a-AMYLASE

EUDAMED

Class C (EU MDR)

Ref 1418-0167Ref 1419-0160Ref 1415-0162

by Medicon Hellas SA

Identity

Trade Name
a-AMYLASE EUDAMED
Device Name
a-AMYLASE EUDAMED
Model / Reference
1418-0167 EUDAMED
1419-0160 EUDAMED
1415-0162 EUDAMED

Identifiers

Primary DI / UDI-DI
05204309031320 EUDAMED
05204309161348 EUDAMED
05204309171453 EUDAMED
Basic UDI-DI
5204309000001NC EUDAMED
Direct Marketing DI
05204309031320 EUDAMED
05204309161348 EUDAMED
05204309171453 EUDAMED
EMDN Code
W01010107 AMYLASE - TOTAL EUDAMED

Classification

Device Class
Class C 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

a-AMYLASE 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 (3)

  • EUDAMED a860adbe-ffcd-41ac-b825-f8e542169970 61 fields · synced Sep 30, 2026
  • EUDAMED 71ce4ce3-c117-4681-a771-91c2ead7a408 61 fields · synced May 17, 2026
  • EUDAMED 90a9604a-b978-4d0c-a55b-c36d81dba8ac 61 fields · synced May 18, 2026