Omnilink Elite Peripheral Stent System - FDA Registration 8171394536ea2375bbf49d70020cbe75

Access comprehensive regulatory information for Omnilink Elite Peripheral Stent System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8171394536ea2375bbf49d70020cbe75 and manufactured by Abbott Vascular. The device was registered on April 18, 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.