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Quantia A-1-AGP

EUDAMED

Class B (EU MDR)

Ref 6L34-43

by Biokit S.A.

Identity

Trade Name
Quantia A-1-AGP EUDAMED
Device Name
Quantia A-1-AGP EUDAMED
Model / Reference
6L34-43 EUDAMED

Identifiers

Primary DI / UDI-DI
00380740157425 EUDAMED
Basic UDI-DI
8436003070252X5 EUDAMED
EMDN Code
W0102019001 A1-ACID GLYCOPROTEIN (OROSOMUCOID) EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Spain 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

Quantia A-1-AGP by Biokit, S.a. — 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
Biokit S.A.
EUDAMED SRN
ES-MF-000002406

Sources (1)

  • EUDAMED c3476d6c-12a1-4f26-b645-100b6c0a99c3 61 fields · synced Jun 18, 2026