AAXON ND DUAL CHANNEL IMPLANTABLE PULSE GENERATOR KIT FOR DEEP BRAIN STIMULATION (DBS) - FDA Registration MDR-07642

Access comprehensive regulatory information for AAXON ND DUAL CHANNEL IMPLANTABLE PULSE GENERATOR KIT FOR DEEP BRAIN STIMULATION (DBS) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07642 and manufactured by SceneRay Co., Ltd. in China. The device was registered on June 24, 2020.

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.