Coronary Stent System Coroflex ISAR Neo - FDA Registration cb03ded7fd77bf8559dee1b9cbfbd7a7

Access comprehensive regulatory information for Coronary Stent System Coroflex ISAR Neo in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cb03ded7fd77bf8559dee1b9cbfbd7a7 and manufactured by B.Braun Melsungen AG. The device was registered on November 03, 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.