Myanmar FDA registration 6a8fdde18f89e1596cef841e6fde8d27

Endoscopic Ultrasound System

Myanmar·FUJIFILM·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered September 15, 2022

Device classification

Brand Name: FUJIFILM

Registration information

Analysis ID: 6a8fdde18f89e1596cef841e6fde8d27
Registration Date: September 15, 2022

Manufacturer

Name: FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office

Authorized Representative

Name: SEA LION COMPANY LIMITED

About this record

Access comprehensive regulatory information for Endoscopic Ultrasound System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6a8fdde18f89e1596cef841e6fde8d27 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on September 15, 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.