PreviscAid® Sodium Hyaluronate & Sodium Chondroitin Sulfate Ophthalmic Viscoelastic - FDA Registration CMDR-2024-03579

Access comprehensive regulatory information for PreviscAid® Sodium Hyaluronate & Sodium Chondroitin Sulfate Ophthalmic Viscoelastic in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03579 and manufactured by Maxigen Biotech Inc. no. 88 Keji 1st Road, Guishan District, Taoyuan City 33383, Taiwan in Taiwan. The device was registered on December 20, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (I-Senz Medical, 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.