Syphilis Ab Rapid Test Cassette (Whole Blood / Serum / Plasma) - FDA Registration e72e008c30d6d1d54aff26423d664706

Access comprehensive regulatory information for Syphilis Ab 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 e72e008c30d6d1d54aff26423d664706 and manufactured by Qingdao Hightop Biotech Co.,Ltd. The device was registered on November 10, 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.