Titanium Ventilation Tube

Access comprehensive regulatory information for Titanium Ventilation Tube in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10031 and manufactured by Spiggle & Theis Medizintechnik GmbH - Burghof 14, 51491 Overath, Germany in Germany. The device was registered on June 08, 2022.

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.