MYCOPLASMA DETECTION BY NA REAGENTS

Primary DI

06976055490063

Basic UDI-DI Code

B-06976055490063

Reference

NA

Device Types

Single use

Regulation

Eu Ivdd

Classification

Eu Ivd General

Status

On The Market

Manufacturer

GUANGZHOU DEAOU GENE TECHNOLOGY CO., LTD

This kit is used for qualitative detection of mycoplasma pneumoniae and chlamydia pneumoniae nucleic acids in throat swab samples. This product is an in vitro diagnostic reagent of real-time fluorescence PCR running on ARTIS system. The detection results are only used for clinical auxiliary diagnosis, and cannot be used as the basis for diagnosis or exclusion of cases alone.

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