GONOCOCCAL DETECTION BY NA REAGENTS

Primary DI

06928103011911

Basic UDI-DI Code

B-06928103011911

Reference

DA1191

Device Types

Single use

Regulation

Eu Ivdd

Classification

Eu Ivd General

Status

On The Market

Manufacturer

Daan Gene Co., Ltd.

This kit is intended for the qualitative detection of Neisseria gonorrhoeae nucleic acid in male urethral secretion swabs and female cervical secretion swabs. This kit is used for supplementary diagnosis of Neisseria gonorrhoeae infection, only for clinical reference, and cannot be used as the sole basis for definitive diagnosis or exclusion of cases.

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