1-DAY ACUVUE MOIST - FDA Registration 5d795e9429815cacc28a303b3eed9bbe

Access comprehensive regulatory information for 1-DAY ACUVUE MOIST in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5d795e9429815cacc28a303b3eed9bbe and manufactured by Johnson & Johnson Vision Care, Inc. (USA). The device was registered on March 24, 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.