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Acuvue 2 - FDA Registration 762336f385059a5c1734ece8620cb679

Access comprehensive regulatory information for Acuvue 2 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 762336f385059a5c1734ece8620cb679 and manufactured by Johnson & Johnson Vision Care, Inc. (USA). The device was registered on October 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.

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762336f385059a5c1734ece8620cb679
Acuvue 2
FDA ID: 762336f385059a5c1734ece8620cb679
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Device Classification
Brand Name
ACUVUE
Registration Information
Analysis ID
762336f385059a5c1734ece8620cb679
Registration Date
October 18, 2022