ASAHI PTCA Guide Wire SION Blue ES Pre-shape - FDA Registration CMDR-2024-03299

Access comprehensive regulatory information for ASAHI PTCA Guide Wire SION Blue ES Pre-shape in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03299 and manufactured by ASAHI INTECC CO., LTD. - 3-100 Akatsuki-cho, Seto Aichi 489-0071 Japan Mfd by: ASAHI INTECC (THAILAND) CO., LTD. - 158/1 Moo 5, Bangkadi Industrial Park, Tiwanon Road, Tambol Bangkadi Amphur Muang, Pathumthani, Pathumthani 12000, Thailand in Thailand. The device was registered on October 18, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Medifaith Medical Enterprises 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.