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Biomime Aura Sirolimus Eluting Coronary Stent System - FDA Registration b967a19f6f76b4103ea1d96b6f8b3875

Access comprehensive regulatory information for Biomime Aura Sirolimus Eluting Coronary Stent System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b967a19f6f76b4103ea1d96b6f8b3875 and manufactured by Meril Life Sciences Pvt. Ltd.. The device was registered on October 28, 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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b967a19f6f76b4103ea1d96b6f8b3875
Biomime Aura Sirolimus Eluting Coronary Stent System
FDA ID: b967a19f6f76b4103ea1d96b6f8b3875
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Device Classification
Brand Name
Biomime Aura
Registration Information
Analysis ID
b967a19f6f76b4103ea1d96b6f8b3875
Registration Date
October 28, 2022
Authorized Representative