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May-Grunwald's Giemsa Stain (for Autostainer)

by BaSO Biotech Co., LTD.. 6 variants

Ref MGG-140

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number471988911HematologyD8 Basic UDI-DI 04719889110910UDI-DIDate9 Jun 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Hematology
Model / Reference
MGG-140
Primary DI / UDI-DI
04719889110910
Basic UDI-DI
471988911HematologyD8
EMDN Code
W0103010399 Haematology stains for microscopy - other
Device Class
Class A
EU market of registration
Italy

Manufacturer details

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

Other devices from BaSO Biotech Co., LTD..

See all devices from BaSO Biotech Co., LTD.. →

Properties

  • Reagent
  • Professional Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No