ALLPLEX™ VAGINITIS SCREENING ASSAY - MDA Registration IVDC2895724-163278
Access comprehensive regulatory information for ALLPLEX™ VAGINITIS SCREENING ASSAY in the Malaysia medical device market through Pure Global AI's free database. This C medical device is registered under MDA ID IVDC2895724-163278 with brand name ALLPLEX™. The device was registered on February 05, 2024.
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
IVDC2895724-163278
ALLPLEX™ VAGINITIS SCREENING ASSAY
MDA ID: IVDC2895724-163278
Device Classification
Risk Class
C
Brand Name
ALLPLEX™
Registration Information
Analysis ID
IVDC2895724-163278
Registration Date
February 05, 2024
Expiration Date
February 04, 2029
Authorized Representative
Type
Authorised Representative;Distributor;Importer

