Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

Tuberculosis Rapid Test (Whole Blood/Serum/Plasma)

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

Basic Information

Primary DI
06976753475843
Basic UDI-DI Code
B-06976753475843
Reference
A480501T
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

Tuberculosis Rapid Test (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of anti-TB antibodies (lsotypes lgG, lgM and lgA) in whole blood, serum or plasma specimens.

CND Nomenclature Codes

Code Description
W0105010799 MYCOBACTERIA REAGENTS - OTHER

Similar Devices

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

View all