iCheck Ecstasy (MDMA) Rapid Test cassette (Urine)

Access comprehensive regulatory information for iCheck Ecstasy (MDMA) Rapid Test cassette (Urine) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00924 and manufactured by Hangzhou AllTest Biotech Co., Ltd. in China. The device was registered on February 13, 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.