Dengue IgM / IgG Rapid Test Cassette (Whole Blood/ Serum/ Plasma) - FDA Registration adc7f3c380a24a0f45d6a47acebf011f
Access comprehensive regulatory information for Dengue IgM / IgG Rapid Test Cassette (Whole Blood/ Serum/ Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID adc7f3c380a24a0f45d6a47acebf011f and manufactured by Qingdao Hightop Biotech Co.,Ltd. The device was registered on November 26, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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adc7f3c380a24a0f45d6a47acebf011f
Dengue IgM / IgG Rapid Test Cassette (Whole Blood/ Serum/ Plasma)
FDA ID: adc7f3c380a24a0f45d6a47acebf011f
Device Classification
Brand Name
KANGHUA
Registration Information
Analysis ID
adc7f3c380a24a0f45d6a47acebf011f
Registration Date
November 26, 2022
Manufacturer
Authorized Representative

