TUBAVENT® Balloon Catheter for the Tuba Eustachii

Access comprehensive regulatory information for TUBAVENT® Balloon Catheter for the Tuba Eustachii in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10722B and manufactured by Spiggle & Theis Medizintechnik GmbH - Burghof 14, 51491 Overath, Germany in Germany. The device was registered on September 02, 2022.

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