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IgA

EUDAMED

Class B (EU MDR)

Ref 3000-2268

by Biokit S.A.

Identity

Trade Name
IgA EUDAMED
Device Name
IgA EUDAMED
Model / Reference
3000-2268 EUDAMED

Identifiers

Primary DI / UDI-DI
08426950036944 EUDAMED
Basic UDI-DI
842695003694476 EUDAMED
EMDN Code
W0102010101 IMMUNOGLOBULIN A 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

IgA 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 531d1103-7b14-4243-8666-1810a9038878 61 fields · synced Jun 19, 2026