CAREPLUS™ INFUSION SET (STERILE) - FDA Registration MDR-09428

Access comprehensive regulatory information for CAREPLUS™ INFUSION SET (STERILE) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09428 and manufactured by Zibo Qray International Co., Ltd. Shandong, China in China. The device was registered on January 26, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Value-Rx, 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.