Wego Extracorporeal Blood Circuit for blood Purification Equipment - FDA Registration CMDR-2022-00980

Access comprehensive regulatory information for Wego Extracorporeal Blood Circuit for blood Purification Equipment in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2022-00980 and manufactured by WEGO Healthcare (Shenzhen) Co., Ltd. Unit 2503, East Technology Mansion, No. 16 Keyuan Road, Nanshan District, Shenzhen China Mfd. By: Weihai Weigao Blood Purification Products Co., Ltd. - No. 20 Xingshan, Shandong Province, People's Republic of China in China. The device was registered on October 05, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Pinnacle Supplies and Services Unlimited, 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.