IHC Diluent - FDA Registration a15c16ae3b2ebe958985da4d4cbe99bd

Access comprehensive regulatory information for IHC Diluent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a15c16ae3b2ebe958985da4d4cbe99bd and manufactured by Leica Biosystems Newcastle Ltd. The device was registered on October 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.