Rapid Latex Kit - FDA Registration a0c4d90adfdcb27b1595870f5fe63c34

Access comprehensive regulatory information for Rapid Latex Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a0c4d90adfdcb27b1595870f5fe63c34 and manufactured by Lorne Laboratories Ltd. The device was registered on September 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.