Dual Top Anchor System - FDA Registration 479d74897a0c494cebd547f24951e7f6

Access comprehensive regulatory information for Dual Top Anchor System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 479d74897a0c494cebd547f24951e7f6 and manufactured by Jeil Medical Corporation. The device was registered on June 22, 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.