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Dri-Sate® Dry Acid Concentrate (45X) - FDA Registration CMDR-2024-03567

Access comprehensive regulatory information for Dri-Sate® Dry Acid Concentrate (45X) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03567 and manufactured by Rockwell Medical, Inc. 30142 Wixom Road, Wixom MI 48393, United States of America Mfd by: Rockwell Medical, Inc. 4051 Freeport Parkway Suite 100 Grapevine Texas 7605 1 USA in USA. The device was registered on December 18, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Berovan Marketing, Inc.), 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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USA
CMDR-2024-03567
Dri-Sate® Dry Acid Concentrate (45X)
Registered medical device in Philippines
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Device Information
Product Name
Dri-Sate® Dry Acid Concentrate (45X)
Registration Number
CMDR-2024-03567
Importer & Distribution
Importer/Distributor
Berovan Marketing, Inc.
Registration Dates
Issuance Date
December 18, 2024
Expiry Date
December 18, 2029