Beright AMP500 Rapid Test Cassette (Urine) - FDA Registration IVDR-00729

Access comprehensive regulatory information for Beright AMP500 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-00729 and manufactured by Hangzhou AllTest Biotech Co., Ltd. 550# Yinhai Street Hangzhou Economic and Technolgical Development Area 310018 Hangzhou People's Republic of China in China. The device was registered on November 08, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Worldbridge Phils. Inc.), 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.