UDI-DI variants

2 UDI-DI variants

Data from EUDAMED, last updated May 23, 2026

Galileo NEO / NEO Iris

88823405W0202030102A52HY

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: IMMUCOR Medizinische Diagnostik GmbH

2 UDI-DI variants

Professional testing

Basic UDI-DI: 88823405W0202030102A52HY
Device name: Galileo NEO / NEO Iris
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jun 15, 2022