ALKALINE PHOSPHATASE (ALP)

Primary DI

05204309161188

Basic UDI-DI Code

5204309000006NN

Reference

1419-0130

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 Alkaline Phosphatase (EC 3.1.3.1), in samples of human serum or plasma from the general patient population. Measurements of Alkaline Phosphatase are intended to be used by licensed physicians, along with other in vitro and in vivo tests and physical examination, as an aid for diagnosis and management of disorders with liver and/or bone involvement.

The Basic UDI-DI associated with this device has 5 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).