XTREME PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY GUIDEWIRE - FDA Registration MDR-09558C

Access comprehensive regulatory information for XTREME PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY GUIDEWIRE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09558C 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 May 28, 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.