ASO LATEX TEST - FDA Registration 9fdd3a0bc98b6c4d117b53b5475f38cc

Access comprehensive regulatory information for ASO LATEX TEST in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9fdd3a0bc98b6c4d117b53b5475f38cc and manufactured by Lab-Care Diagnostics (India) Pvt. Ltd.. The device was registered on November 15, 2021.

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.