UDI-DI variants

2 UDI-DI variants

Data from EUDAMED, last updated May 31, 2026

WES pro

764041338C4130UR

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: 4bases SA

ReagentProfessional testing

Basic UDI-DI: 764041338C4130UR
Device name: WES pro
Device model: WES pro
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 28, 2026