Sure-Guard® Manual Resuscitator Silicon - FDA Registration CMDR-2024-02955

Access comprehensive regulatory information for Sure-Guard® Manual Resuscitator Silicon in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02955 and manufactured by La-Med Healthcare Pvt. Ltd. Plot No. 136, Sector -24, N.I.T. Faridabad - 121005, Haryana, India in India. The device was registered on June 05, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (AMB HK Enterprises, 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.