Myanmar FDA registration 1cf9d43a93a2f8cf6231260bf34c52b3

Fibreoptic Bronchoscope System

Myanmar·FUJIFILM·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered May 20, 2022

Device classification

Brand Name: FUJIFILM

Registration information

Analysis ID: 1cf9d43a93a2f8cf6231260bf34c52b3
Registration Date: May 20, 2022

Manufacturer

Name: FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office

Authorized Representative

Name: SEA LION COMPANY LIMITED

About this record

Access comprehensive regulatory information for Fibreoptic Bronchoscope System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1cf9d43a93a2f8cf6231260bf34c52b3 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on May 20, 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.