Matrix™ Gel System Diluent - 2 LISS - FDA Registration IVDR-00372

Access comprehensive regulatory information for Matrix™ Gel System Diluent - 2 LISS in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00372 and manufactured by Tulip Diagnostics (P) Ltd. - Gitanjali, Tulip Block, Dr. Antonio Do Rego Bagh, Alto Santacruz, Bambolin Complex P.O., Goa - 403 202, India Mfd by: Tulip Diagnostics (P) Ltd. Plot Nos. 92/96, Phase IIC, Verna Industrial Estate, Verna, Goa - 403 722, India. in India.. The device was registered on May 26, 2025.

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