UNITE CORONARY ANGIOGRAPHY (CAG) CATHETER STERILIZED PRODUCT (TYPE A) - FDA Registration MDR-10771

Access comprehensive regulatory information for UNITE CORONARY ANGIOGRAPHY (CAG) CATHETER STERILIZED PRODUCT (TYPE A) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10771 and manufactured by Toyoflex Cebu Corporation - Lot 14, Block 2, Cebu Light Industrial Park (CLIP), Basak, Lapu-Lapu, Cebu in Philippines. The device was registered on January 13, 2021.

This page provides complete registration details including manufacturer information, importer/distributor details (Toyoflex Cebu Corporation), 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.