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MDKMED MI Infusion Pump - FDA Registration CMDR-2025-04985

Access comprehensive regulatory information for MDKMED MI Infusion Pump in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04985 and manufactured by Zhejiang MDKingdom Technology Co., Ltd. - 4th Floor, 22 Cang Ling Road, Huzhen Town, Jinyun County, 321404 Lishui City, Zhejiang, Province, P. R. of China in China. The device was registered on July 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Josmef Enterprises), 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-2025-04985
MDKMED MI Infusion Pump
Registered medical device in Philippines
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Device Information
Product Name
MDKMED MI Infusion Pump
Registration Number
CMDR-2025-04985
Importer & Distribution
Importer/Distributor
Josmef Enterprises
Registration Dates
Issuance Date
July 10, 2025
Expiry Date
July 10, 2030