Kendall SCD Smartflow™ Compression System - FDA Registration CMDR-2025-04616

Access comprehensive regulatory information for Kendall SCD Smartflow™ Compression System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04616 and manufactured by Cardina1 Health 200, LLC - 3651 Birchwrood Drive, Waukegan, IL 60085 USA Mfd. By: Jabil Circuit (Singapore) Pte. Ltd. - 16 Tampines Industrial Crescent Singapore, 528604 Singapore in USA. The device was registered on May 20, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Lifelink, 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.