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Asahi PTCA Guidewire - FDA Registration DVR-8879

Access comprehensive regulatory information for Asahi PTCA Guidewire in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-8879 and manufactured by Asahi Intecc Co., Ltd. - 3-100 Akatsuki-cho, Seto-Chi, 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 Japan. The device was registered on August 17, 2022.

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

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Japan
DVR-8879
Asahi PTCA Guidewire
Registered medical device in Philippines
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Importer & Distribution
Importer/Distributor
Medifaith Medical Enterprises
Registration Dates
Issuance Date
August 17, 2022
Expiry Date
April 11, 2027