Myanmar FDA registration 1f0053c6c0266856642eac6552dfcb57

HOYA Nanex multiSert + Aspheric Preloaded Intraocular Lens

Myanmar·HOYA Nanex multiSert·HOYA Lamphun Ltd.·Registered February 08, 2022

Device classification

Brand Name: HOYA Nanex multiSert

Registration information

Analysis ID: 1f0053c6c0266856642eac6552dfcb57
Registration Date: February 08, 2022

Manufacturer

Name: HOYA Lamphun Ltd.

Authorized Representative

Name: JSVM COMPANY LIMITED

About this record

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.