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TECNIS Synergy OptiBlue IOL - FDA Registration a2034554c2467be0ec669a4c9e03e3e8

Access comprehensive regulatory information for TECNIS Synergy OptiBlue IOL in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a2034554c2467be0ec669a4c9e03e3e8 and manufactured by AMO Puerto Rico Manufacturing, Inc.. The device was registered on February 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
a2034554c2467be0ec669a4c9e03e3e8
TECNIS Synergy OptiBlue IOL
FDA ID: a2034554c2467be0ec669a4c9e03e3e8
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Device Classification
Brand Name
Johnson & Johnson Vision
Registration Information
Analysis ID
a2034554c2467be0ec669a4c9e03e3e8
Registration Date
February 07, 2022
Authorized Representative