DENGUE NS1 ANTIGEN RAPID TEST CASSETTE (SERUM/PLASMA/WHOLE BLOOD) - MDA Registration IVDC5805423-149442
Access comprehensive regulatory information for DENGUE NS1 ANTIGEN 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 IVDC5805423-149442 with brand name FLOWFLEX. The device was registered on September 27, 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.
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MDA Official Data
C
IVDC5805423-149442
DENGUE NS1 ANTIGEN RAPID TEST CASSETTE (SERUM/PLASMA/WHOLE BLOOD)
MDA ID: IVDC5805423-149442
Device Classification
Risk Class
C
Brand Name
FLOWFLEX
Registration Information
Analysis ID
IVDC5805423-149442
Registration Date
September 27, 2023
Expiration Date
September 26, 2028
Authorized Representative
Type
Authorised Representative;Distributor;Importer

