Asahi Sion PTCA Guide Wire - FDA Registration MDR-01171

Access comprehensive regulatory information for Asahi Sion PTCA Guide Wire in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01171 and manufactured by ASAHI INTECC Co., LTD. 3-100 Akatsuki-cho, Seto Aichi 489-0071, Japan Mfd By: ASAHI INTECC (Thailand)Co., Ltd. - 158/2, Moo 5, Bangkadi Indsutrial Park, Tiwanon Road, Tambol Bangkadi, Amphur Muang Pathumthani, 12000 Pathumthani, Thailand in Japan. The device was registered on May 03, 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.