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Giemsa Solution

EUDAMED

Class A (EU MDR)

Ref MGX-09B

by BaSO Biotech Co., LTD..

Identity

Trade Name
Giemsa Solution EUDAMED
Device Name
Hematology EUDAMED
Model / Reference
MGX-09B EUDAMED

Identifiers

Primary DI / UDI-DI
04719889110873 EUDAMED
Basic UDI-DI
471988911HematologyD8 EUDAMED
EMDN Code
W0103010399 HAEMATOLOGY STAINS FOR MICROSCOPY - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Italy 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 Solution by BaSO Biotech Co., 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

EUDAMED SRN
TW-MF-000018809
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 64555870-c55f-4e17-9ca4-11afbf10eebd 61 fields · synced Jun 19, 2026