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Leishman otopina, 1000 mL

EUDAMED

Class A (EU MDR)

Ref LE-OT-1L

by BioGnost Ltd.

Identity

Trade Name
Leishman otopina, 1000 mL EUDAMED
Device Name
Reagensi za hematologiju EUDAMED
Model / Reference
LE-OT-1L EUDAMED

Identifiers

Primary DI / UDI-DI
03858888822286 EUDAMED
Basic UDI-DI
385889212HPC3010302HMCA EUDAMED
Direct Marketing DI
03858888822286 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, 1000 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 0b7276a2-73f9-41f6-8b96-321a01b913e8 61 fields · synced Jul 15, 2026