1-DAY ACUVUE DEFINE - FDA Registration 0c1a4b4d4e5fded24969e5d420bbceab

Access comprehensive regulatory information for 1-DAY ACUVUE DEFINE in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0c1a4b4d4e5fded24969e5d420bbceab and manufactured by Johnson & Johnson Vision Care, Inc. (USA). The device was registered on October 18, 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.