iCheck HIV 1.2.O Rapid Test Cassette (Whole Blood/ Serum/ Plasma) - FDA Registration IVDR-00954

Access comprehensive regulatory information for iCheck HIV 1.2.O Rapid Test Cassette (Whole Blood/ Serum/ Plasma) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00954 and manufactured by Hangzhou AllTest Biotech Co., Ltd.- 550#, Yinhai Street, Hangzhou Economic and Technological Development Area, 310018 Hangzhou, People's Republic of China in China. The device was registered on April 04, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Philippine Blue Cross Biotech Corporation), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.