JUSCHEK HCG PREGNANCY ENHANCED SENSITIVITY RAPID TEST DIPSTICK (SERUM/PLASMA/URINE) - FDA Registration IVDR-00561

Access comprehensive regulatory information for JUSCHEK HCG PREGNANCY ENHANCED SENSITIVITY RAPID TEST DIPSTICK (SERUM/PLASMA/URINE) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00561 and manufactured by Hangzhou AllTest Biotech Co., Ltd. - Hangzhou, People's Republic of China in China. The device was registered on February 18, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (MGV Sciechem 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.