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Optio Polyethersulfone Hollow Fiber Hemodialyzer, Low Flux - FDA Registration MDR-10768

Access comprehensive regulatory information for Optio Polyethersulfone Hollow Fiber Hemodialyzer, Low Flux in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10768 and manufactured by Chengdu OCI Medical Co., Ltd. - No. 2401 West Airport Road, Southwest Airport Economic Development Zone, Shuangliu District, Chengdu City, Sichuan Province, P.R. China in China. The device was registered on August 30, 2022.

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.

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China
MDR-10768
Optio Polyethersulfone Hollow Fiber Hemodialyzer, Low Flux
Registered medical device in Philippines
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Device Information
Product Name
Optio Polyethersulfone Hollow Fiber Hemodialyzer, Low Flux
Registration Number
MDR-10768
Importer & Distribution
Importer/Distributor
Infilife Corporation
Registration Dates
Issuance Date
August 30, 2022
Expiry Date
January 13, 2027