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Alinity c Digitoxin Reagent Kit

EUDAMED

Class C (EU MDR)

Ref 01R1122

by Biokit S.A.

Identity

Trade Name
Alinity c Digitoxin Reagent Kit EUDAMED
Device Name
Alinity c Digitoxin Reagent Kit EUDAMED
Model / Reference
01R1122 EUDAMED

Identifiers

Primary DI / UDI-DI
00380740153632 EUDAMED
Basic UDI-DI
8436003070610X9 EUDAMED
EMDN Code
W0102080102 DIGITOXIN EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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 Digitoxin Reagent Kit by Biokit, S.a. — 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
Biokit S.A.
EUDAMED SRN
ES-MF-000002406

Sources (1)

  • EUDAMED 29bd0b97-9b69-4532-8f2c-e59639befda3 61 fields · synced Jul 14, 2026