Asahi Peripheral Vascular Guidewire - FDA Registration CMDR-2025-04668

Access comprehensive regulatory information for Asahi Peripheral Vascular Guidewire in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04668 and manufactured by Toyoflex Cebu Corporation - Lot 14, Block 2, Cebu Light Industrial Park (CLIP), Basak, 6015 Lapu-Lapu City, Philippines in Philippines. The device was registered on June 30, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (N/A), 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.