OPTIO Polyethersulfone Hollow Fiber Hemodialyzer, High Flux - FDA Registration CMDR-2025-03936

Access comprehensive regulatory information for OPTIO Polyethersulfone Hollow Fiber Hemodialyzer, High Flux in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03936 and manufactured by Chengdu OCI Medical Devices Co., Ltd. No. 2401 West Port Avenue, South West Airport Economic Development Zone, Shuangliu District, Chengdu, Sichuan Province, 610299, P.R. China in China. The device was registered on February 24, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Infilife Corporation), 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.