SENSATION Intra-aortic Balloon Catheter, Insertion Kit and Connector - FDA Registration 30497594603c294fcfc4cc1cbc9f05eb

Access comprehensive regulatory information for SENSATION Intra-aortic Balloon Catheter, Insertion Kit and Connector in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 30497594603c294fcfc4cc1cbc9f05eb and manufactured by Datascope Corp. The device was registered on October 14, 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.