ANGIOWAY™ MANIFOLD DISPOSABLE INTERVENTIONAL ACCESSORIES (NO EXTENSION TUBING) - FDA Registration MDR-07835A

Access comprehensive regulatory information for ANGIOWAY™ MANIFOLD DISPOSABLE INTERVENTIONAL ACCESSORIES (NO EXTENSION TUBING) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07835A and manufactured by LEPU Medical Technology (Beijing) Co., Ltd. in China. The device was registered on March 25, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (First Associated Medical Distribution Co., 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.