AGANI™ TERUMO NEEDLE - FDA Registration MDR-01346

Access comprehensive regulatory information for AGANI™ TERUMO NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01346 and manufactured by Zhejiang Kindly Medical Devices Co., Ltd. No. 758, 5th Binhai Indsutrial Park, Longwan District 325025 Wenzhou, Zhejiang Province, People's Republic of China in China. The device was registered on June 13, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Terumo Marketing Philippines, 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.