Myanmar FDA registration fa5982b65aecd3ac2e51c76160a8070f
Malaria P.f/P.v Antigen Test
Device classification
- Brand Name
- Humasis
Registration information
- Analysis ID
- fa5982b65aecd3ac2e51c76160a8070f
- Registration Date
- October 26, 2022
Manufacturer
- Name
- Humasis Co.,Ltd
Authorized Representative
About this record
Access comprehensive regulatory information for Malaria P.f/P.v Antigen Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fa5982b65aecd3ac2e51c76160a8070f and manufactured by Humasis Co.,Ltd. The device was registered on October 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.
Free DatabasePowered by Pure Global AIFDA Official Data