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HOYA Nanex multiSert + Aspheric Preloaded Intraocular Lens - FDA Registration 1f0053c6c0266856642eac6552dfcb57

Access comprehensive regulatory information for HOYA Nanex multiSert + Aspheric Preloaded Intraocular Lens in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1f0053c6c0266856642eac6552dfcb57 and manufactured by HOYA Lamphun Ltd.. The device was registered on February 08, 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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1f0053c6c0266856642eac6552dfcb57
HOYA Nanex multiSert + Aspheric Preloaded Intraocular Lens
FDA ID: 1f0053c6c0266856642eac6552dfcb57
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Device Classification
Brand Name
HOYA Nanex multiSert
Registration Information
Analysis ID
1f0053c6c0266856642eac6552dfcb57
Registration Date
February 08, 2022
Manufacturer
Authorized Representative