URETERAL Stent - FDA Registration ae9cbcf2d27158fe06d304b492b07cf2

Access comprehensive regulatory information for URETERAL Stent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ae9cbcf2d27158fe06d304b492b07cf2 and manufactured by Blue Neem Medical Devices Private Limited. The device was registered on February 01, 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.