RapidFor™ Microalbumin Rapid Test Kit (FIA)

Primary DI

08683548250872

Basic UDI-DI Code

B-08683548250872

Reference

VMPO49

Device Types

Single use

Regulation

Eu Ivdd

Classification

Eu Ivd General

Status

On The Market

Manufacturer

Vitrosens Biyoteknoloji Anonim Şirketi

This kit is applicable to the in vitro quantitative test on the concentration of microalbumin (MAU) in human urine samples. The increased excretion of microalbumin (MAU) in urine is an early change of the disease, which has important reference value and clinical significance for the early diagnosis and early treatment of the disease.

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).