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Unimex® Volumetric Infusion Set - FDA Registration MDR-07420

Access comprehensive regulatory information for Unimex® Volumetric Infusion Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07420 and manufactured by Jiangxi Hongda Medical Equipment group Ltd,. 39 South Shengli RD, Jinxian County 331700 Nanchang, Jiangxi Province People's Republic of China in China. The device was registered on December 26, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Progressive Medical 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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MDR-07420
Unimex® Volumetric Infusion Set
Registered medical device in Philippines
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Device Information
Product Name
Unimex® Volumetric Infusion Set
Registration Number
MDR-07420
Importer & Distribution
Registration Dates
Issuance Date
December 26, 2024
Expiry Date
November 16, 2029