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HOYA iSert Preloaded Intraocular Lens - FDA Registration d555fcac78b633054711f8726fd27b13

Access comprehensive regulatory information for HOYA iSert Preloaded Intraocular Lens in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d555fcac78b633054711f8726fd27b13 and manufactured by HOYA LAMPHUN LTD.. The device was registered on August 02, 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
d555fcac78b633054711f8726fd27b13
HOYA iSert Preloaded Intraocular Lens
FDA ID: d555fcac78b633054711f8726fd27b13
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Device Classification
Brand Name
HOYA iSert
Registration Information
Analysis ID
d555fcac78b633054711f8726fd27b13
Registration Date
August 02, 2022
Manufacturer
Authorized Representative