FSH Rapid Quantitative Test - FDA Registration 8faa40698f13b5d7ffc6d249786a8a4c

Access comprehensive regulatory information for FSH Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8faa40698f13b5d7ffc6d249786a8a4c and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on September 09, 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.