Canack Endotracheal Tube - FDA Registration CMDR-2025-03758A

Access comprehensive regulatory information for Canack Endotracheal Tube in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03758A and manufactured by Ningbo Luke Medical Devices Co., Ltd. in China. The device was registered on January 31, 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.