MANI SUTURE PGA OPTHALMIC SUTURE - FDA Registration MDR-08010

Access comprehensive regulatory information for MANI SUTURE PGA OPTHALMIC SUTURE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08010 and manufactured by Mani, Inc. - 8-3 Kiyohara Industrial Park, Utsunomiya, Tochigi, 321-3231, Japan in Japan. The device was registered on June 13, 2025.

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.