Everolimus-Eluting Platinum Chromium Coronary Stent System (SYNERGY MONORAIL) - FDA Registration 696c622a31cfaf6f9fbed0f31b84a1ed
Access comprehensive regulatory information for Everolimus-Eluting Platinum Chromium Coronary Stent System (SYNERGY MONORAIL) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 696c622a31cfaf6f9fbed0f31b84a1ed and manufactured by Boston Scientific Limited.. The device was registered on July 07, 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.
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FDA Official Data
696c622a31cfaf6f9fbed0f31b84a1ed
Everolimus-Eluting Platinum Chromium Coronary Stent System (SYNERGY MONORAIL)
FDA ID: 696c622a31cfaf6f9fbed0f31b84a1ed
Device Classification
Brand Name
Boston Scientific Brand
Registration Information
Analysis ID
696c622a31cfaf6f9fbed0f31b84a1ed
Registration Date
July 07, 2022
Manufacturer
Authorized Representative

