Ruschelit® Safety Clear Plus Tracheal Tube - FDA Registration DVR-8767

Access comprehensive regulatory information for Ruschelit® Safety Clear Plus Tracheal Tube in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-8767 and manufactured by Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone Co. Westmeath, Ireland Mfd By: Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone, Co. Westmeath, Ireland Mfd By: Teleflex Cor. Roosevelt Sdn-Kamunting Perak, Malaysia in Ireland. The device was registered on May 09, 2024.

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