THE LATEX TEST KIT - FDA Registration 4d009626ab47d49de6056537d03ebc7e

Access comprehensive regulatory information for THE LATEX TEST KIT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4d009626ab47d49de6056537d03ebc7e and manufactured by Lorne Laboratories Limited. The device was registered on August 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.