LDH (P-L) Kit - FDA Registration c00ae5f2821e652ec37c06664657a508

Access comprehensive regulatory information for LDH (P-L) Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c00ae5f2821e652ec37c06664657a508 and manufactured by Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd.. The device was registered on May 20, 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.