H. pylori Antibody Rapid Test Cassette (Whole Blood/Serum/Plasma) - FDA Registration 838459f501eedd758b51f95e41981c87

Access comprehensive regulatory information for H. pylori Antibody 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 838459f501eedd758b51f95e41981c87 and manufactured by Hangzhou AllTest Biotech Co., Ltd. The device was registered on October 17, 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.