GGT

Primary DI

05204309174164

Basic UDI-DI Code

5204309000024NQ

Reference

1415-0102

Device Types

None provided

Regulation

Eu Ivdr

Classification

Eu Ivd Class B

Status

On The Market

Manufacturer

Medicon Hellas SA

Reagent kit for In Vitro quantitative automated determination by trained laboratory professionals of the activity of gamma glutamyl-transferase (EC 2.3.2.2), in samples of human serum or plasma from the general patient population. Measurements of GGT are intended to be used by licensed physicians, along with other in vitro and in vivo tests and physical examination, as an aid in the diagnosis of liver diseases, the differentiation between liver and bone-derived elevations of alkaline phosphatase levels, and the detection of alcohol abuse.

The Basic UDI-DI associated with this device has 4 devices in total. Below are some other devices sharing the same Basic UDI-DI.

Other on-the-market devices with the same classification (Eu Ivd Class B) and regulation (EU IVDR).