UDI-DI variants

47 UDI-DI variants

No registered UDI-DI variants for this device family.

Data from EUDAMED, last updated May 23, 2026

Buffer, TCA

6438153BU0001138F

47 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: Thermo Fisher Scientific Oy

Professional testing

Basic UDI-DI: 6438153BU0001138F
Device name: Buffer, TCA
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 25, 2022

47 UDI-DI variants

No registered UDI-DI variants for this device family.