MEGA Intra-Aortic Balloon Catheter and Insertion Kit - FDA Registration 79074c93bb03f362ec3e114b0462ae93

Access comprehensive regulatory information for MEGA Intra-Aortic Balloon Catheter and Insertion Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 79074c93bb03f362ec3e114b0462ae93 and manufactured by Datascope Corp. The device was registered on November 19, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.