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Optio Polyethersulfone Hollow Hemodialyzer, Low Flux - FDA Registration CMDR-2025-03810

Access comprehensive regulatory information for Optio Polyethersulfone Hollow Hemodialyzer, Low Flux in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03810 and manufactured by Chengdu OCI Medical Co., Ltd in China. The device was registered on February 04, 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.

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China
CMDR-2025-03810
Optio Polyethersulfone Hollow Hemodialyzer, Low Flux
Registered medical device in Philippines
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Device Information
Product Name
Optio Polyethersulfone Hollow Hemodialyzer, Low Flux
Registration Number
CMDR-2025-03810
Manufacturer Details
Country of Origin
China
Importer & Distribution
Importer/Distributor
Infilife Corporation
Registration Dates
Issuance Date
February 04, 2025
Expiry Date
February 04, 2030