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LeukoGnost ACP, za 50 testiranja

EUDAMED

Class A (EU MDR)

Ref LKG-ACP

by BioGnost Ltd.

Identity

Trade Name
LeukoGnost ACP, za 50 testiranja EUDAMED
Device Name
Reagensi za citokemiju EUDAMED
Model / Reference
LKG-ACP EUDAMED

Identifiers

Primary DI / UDI-DI
03858892122440 EUDAMED
Basic UDI-DI
385889212HPC30702CYTOS9 EUDAMED
Direct Marketing DI
03858892122440 EUDAMED
EMDN Code
W01030702 CYTOCHEMICAL STAINING REAGENTS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Croatia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

LeukoGnost ACP, za 50 testiranja by BioGnost Ltd. — Class A — 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
BioGnost Ltd.
EUDAMED SRN
HR-MF-000022153

Sources (1)

  • EUDAMED b5564d5f-2509-4ef0-a01d-7f26dd31c5cb 61 fields · synced Jul 26, 2026