Dengue Combo Test - FDA Registration ddd2b487c74ed33a337686200e4e1840
Access comprehensive regulatory information for Dengue Combo Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ddd2b487c74ed33a337686200e4e1840 and manufactured by Humasis Co.,Ltd. The device was registered on April 04, 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.
Free Database
Powered by Pure Global AI
FDA Official Data
ddd2b487c74ed33a337686200e4e1840
Dengue Combo Test
FDA ID: ddd2b487c74ed33a337686200e4e1840
Device Classification
Brand Name
Humasis
Registration Information
Analysis ID
ddd2b487c74ed33a337686200e4e1840
Registration Date
April 04, 2022
Manufacturer
Name
Humasis Co.,LtdAuthorized Representative

