VASSALLO GT Extension Guidewire Extension - FDA Registration CMDR-2023-01703

Access comprehensive regulatory information for VASSALLO GT Extension Guidewire Extension in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-01703 and manufactured by FILMECC CO., LTD - 17033 Wakita-Cho, Moriyama-Kun, Nagoya-Shi, Aichi 463-0024 Japan Mfd. By: Toyoflex Cebu Corporation - Lot 14, Block 2, Cebu Light Industrial Park (CLIP), Basak, 6015 Lapu-Lapu in Philippines. The device was registered on June 22, 2023.

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.