RF LATEX TEST KIT - FDA Registration 898ca98c0b8d2f663e2d3888763eb913

Access comprehensive regulatory information for RF LATEX TEST KIT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 898ca98c0b8d2f663e2d3888763eb913 and manufactured by Lab-Care Diagnostics (India) Pvt. Ltd.. The device was registered on November 12, 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.