DENGUE IGG/IGM RAPID TEST CASSETTE (SERUM/PLASMA/WHOLE BLOOD) - MDA Registration IVDC3392323-151107
Access comprehensive regulatory information for DENGUE IGG/IGM RAPID TEST CASSETTE (SERUM/PLASMA/WHOLE BLOOD) in the Malaysia medical device market through Pure Global AI's free database. This C medical device is registered under MDA ID IVDC3392323-151107 with brand name FLOWFLEX. The device was registered on October 14, 2023.
This page provides complete registration details including authorized representative details, brand information, and regulatory compliance data from the official Malaysia MDA medical device database. Pure Global AI offers free access to Malaysia's complete medical device registry.
Free Database
Powered by Pure Global AI
MDA Official Data
C
IVDC3392323-151107
DENGUE IGG/IGM RAPID TEST CASSETTE (SERUM/PLASMA/WHOLE BLOOD)
MDA ID: IVDC3392323-151107
Device Classification
Risk Class
C
Brand Name
FLOWFLEX
Registration Information
Analysis ID
IVDC3392323-151107
Registration Date
October 14, 2023
Expiration Date
October 13, 2028
Authorized Representative
Type
Authorised Representative;Distributor;Importer

