Sterile Dual Top Anchor System - FDA Registration 8b834ef843ea44c6e78e6361d4badf06

Access comprehensive regulatory information for Sterile 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 8b834ef843ea44c6e78e6361d4badf06 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.