ONE STEP SYPHILIS CARD TEST (SYPHILIS SERUM / PLASMA TEST) - FDA Registration 8776a3c8b541237727d4846e7c88a14c

Access comprehensive regulatory information for ONE STEP SYPHILIS CARD TEST (SYPHILIS SERUM / PLASMA TEST) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8776a3c8b541237727d4846e7c88a14c and manufactured by Lab-Care Diagnostics (I) Pvt. Ltd.. The device was registered on December 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.