Trimera™ Leptospira IgG/ IgM Rapid Test Cassette - FDA Registration IVDR-00730

Access comprehensive regulatory information for Trimera™ Leptospira IgG/ IgM Rapid Test Cassette in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00730 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 March 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Chemtech Medical Supply), 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.