HIV 1.2 Rapid Test Cassette (Whole Blood/ Serum/ Plasma) - FDA Registration 8ad70b0e445204c6494fcc7d00b463d5

Access comprehensive regulatory information for HIV 1.2 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 8ad70b0e445204c6494fcc7d00b463d5 and manufactured by Hangzhou AllTest Biotech Co., Ltd.. The device was registered on April 28, 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.