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Giemsa boja u prahu, 50 g

EUDAMED

Class A (EU MDR)

Ref G-P-50

by BioGnost Ltd.

Identity

Trade Name
Giemsa boja u prahu, 50 g EUDAMED
Device Name
Boje u prahu EUDAMED
Model / Reference
G-P-50 EUDAMED

Identifiers

Primary DI / UDI-DI
03858888820879 EUDAMED
Basic UDI-DI
385889212HPC30707PDYETD EUDAMED
Direct Marketing DI
03858888820879 EUDAMED
EMDN Code
W01030707 STAIN POWDERS (HISTOLOGY/CYTOLOGY) 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

Giemsa boja u prahu, 50 g 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 02f9fea5-79bf-48c6-a356-f238f7f8da56 61 fields · synced Jul 15, 2026