Scalp Vein Set for single use - FDA Registration 51858d6ed504a13c44498471ba583dda

Access comprehensive regulatory information for Scalp Vein Set for single use in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 51858d6ed504a13c44498471ba583dda and manufactured by Yunnan Haodi Medical Instrument Co.,Ltd. The device was registered on July 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.