Eu Ivdd Eu Ivd General On The Market 🇹🇷 Türkiye

RapidFor™ Neisseria Gonorrhoeae Rapid Test Kit

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
08683347941452
Basic UDI-DI Code
B-08683347941452
Reference
VMD39
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

Neisseria Gonorrhoeae Rapid Test Kit is a rapid chromatographic immunoassay for the qualitative detection of Neisseria gonorrhoeae in female cervical swab and male urethral swab specimens to aid in the diagnosis of Gonorrhea infection.

CND Nomenclature Codes

Code Description
W0105010201 GONOCOCCAL ANTIGEN DETECTION

Similar Devices

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

View all