H.PYLORI RAPID TEST KIT (FOR DETECTION OF "H.PYLORI" ANTIBODY)) - FDA Registration e64a0832c7d918cf139e1bfde3091804

Access comprehensive regulatory information for H.PYLORI RAPID TEST KIT (FOR DETECTION OF "H.PYLORI" ANTIBODY)) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e64a0832c7d918cf139e1bfde3091804 and manufactured by Lab-Care Diagnostics (I) Pvt. Ltd.. The device was registered on November 22, 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.