Philippines FDA registration CMDR-2025-04575

ASAHI Peripheral Guidewire Gladius Pre-shape

Philippines·ASAHI INTECC CO., LTD. 3-100 Akatsuki-cho, Seto-shi, 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·Japan·Issued May 08, 2025 – May 08, 2030

Device information

Product Name: ASAHI Peripheral Guidewire Gladius Pre-shape
Registration Number: CMDR-2025-04575

Manufacturer details

Manufacturer: ASAHI INTECC CO., LTD. 3-100 Akatsuki-cho, Seto-shi, 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
Country of Origin: Japan

Importer & distribution

Importer/Distributor: Medifaith Medical Enterprises Inc.

Registration dates

Issuance Date: May 08, 2025
Expiry Date: May 08, 2030

About this record

Access comprehensive regulatory information for ASAHI Peripheral Guidewire Gladius Pre-shape in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04575 and manufactured by ASAHI INTECC CO., LTD. 3-100 Akatsuki-cho, Seto-shi, 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 May 08, 2025.

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.