← Back to catalogue

Alinity c IgE Reagent Kit

EUDAMED

Class B (EU MDR)

Ref 01R1322

by Biokit S.A.

Identity

Trade Name
Alinity c IgE Reagent Kit EUDAMED
Device Name
Alinity c IgE Reagent Kit EUDAMED
Model / Reference
01R1322 EUDAMED

Identifiers

Primary DI / UDI-DI
08436003070405 EUDAMED
Basic UDI-DI
8436003070405X6 EUDAMED
EMDN Code
W01020201 IMMUNOGLOBULIN E - TOTAL 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

Alinity c IgE Reagent Kit 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biokit S.A.
EUDAMED SRN
ES-MF-000002406

Sources (1)

  • EUDAMED d495757d-e3da-4001-af10-70d8f5465004 61 fields · synced Jun 17, 2026