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Leishman otopina, 100 mL

EUDAMED

Class A (EU MDR)

Ref LE-OT-100

by BioGnost Ltd.

Identity

Trade Name
Leishman otopina, 100 mL EUDAMED
Device Name
Reagensi za hematologiju EUDAMED
Model / Reference
LE-OT-100 EUDAMED

Identifiers

Primary DI / UDI-DI
03858888822262 EUDAMED
Basic UDI-DI
385889212HPC3010302HMCA EUDAMED
Direct Marketing DI
03858888822262 EUDAMED
EMDN Code
W0103010302 ROMANOWSKY STAINS 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

Leishman otopina, 100 mL 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 207695a5-b0d4-4207-b82e-66b9867fd42e 61 fields · synced Jul 9, 2026