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HemosIL HIT- Ab(PF4-H) Controls

EUDAMED

Class B (EU MDR)

Ref 0020013300

by Biokit S.A.

Identity

Trade Name
HemosIL HIT- Ab(PF4-H) Controls EUDAMED
Device Name
HemosIL HIT-Ab(PF4-H) EUDAMED
Model / Reference
0020013300 EUDAMED

Identifiers

Primary DI / UDI-DI
08426950584940 EUDAMED
Basic UDI-DI
8426950584971AK EUDAMED
EMDN Code
W0103020615 COAGULATION INHIBITORS/THROMBOPHILIA MARKERS FOR HEPARIN INDUCED THROMBOCYTOPENIA TEST (HIT) EUDAMED

Classification

Device Class
Class B 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

HemosIL HIT- Ab(PF4-H) Controls 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 3853abdf-0e06-422c-8493-5f9578d8c12b 61 fields · synced Jul 14, 2026