Heidi Mein Tourniquet 2 Channel with Printer - FDA Registration CMDR-2024-02235
Access comprehensive regulatory information for Heidi Mein Tourniquet 2 Channel with Printer in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02235 and manufactured by ATMOS MedizinTechnik GmbH & Co. KG Ludwig-Kegel-Straฮฒe 16, 79853 Lenzkirch, Germany Mfd By: Ulrich GmbH & Co. KG - Buchbrunnenweg 12 89081 Ulm, Germany in Germany. The device was registered on January 11, 2024.
This page provides complete registration details including manufacturer information, importer/distributor details (Dubbel 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.
