Myanmar FDA registration d555fcac78b633054711f8726fd27b13

HOYA iSert Preloaded Intraocular Lens

Myanmar·HOYA iSert·HOYA LAMPHUN LTD.·Registered August 02, 2022

Device classification

Brand Name: HOYA iSert

Registration information

Analysis ID: d555fcac78b633054711f8726fd27b13
Registration Date: August 02, 2022

Manufacturer

Name: HOYA LAMPHUN LTD.

Authorized Representative

Name: JSVM COMPANY LIMITED

About this record

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.