Squamous Cell Carcinoma (eCLIA) - FDA Registration e921b29a0b939b998e5cd4ed3e9a8c7a

Access comprehensive regulatory information for Squamous Cell Carcinoma (eCLIA) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e921b29a0b939b998e5cd4ed3e9a8c7a and manufactured by Shenzhen Lifotronic Technology Co.,Ltd. The device was registered on March 27, 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.