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MDT Plus 4 Cold Sterilant - FDA Registration CMDR-2023-01837

Access comprehensive regulatory information for MDT Plus 4 Cold Sterilant in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-01837 and manufactured by Meditop Co., Ltd. - 334 Soi Lat Phrao 71 (Sangkomsong Krawnua 1), Khlong Chaokhun Sing, Wang Thonglang, Bangkok 10310, Thailand Mfd. By: Thai Peroxide Co., Ltd. - 70 Moo 4, Sudbantad Road, Tambol Tandiew, Amphur Kaengkhoi, Saraburi 18110 - Thailand in Thailand. The device was registered on August 09, 2023.

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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Thailand
CMDR-2023-01837
MDT Plus 4 Cold Sterilant
Registered medical device in Philippines
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Importer & Distribution
Importer/Distributor
Infilife Corporation
Registration Dates
Issuance Date
August 09, 2023
Expiry Date
August 09, 2028