Myanmar FDA registration 7806ce9c91f3caaefd01a1f71a8e81c7

Diagnostic X-ray System

Myanmar·Fujifilm·DRGEM CORPORATION·Registered December 30, 2021

Device classification

Brand Name: Fujifilm

Registration information

Analysis ID: 7806ce9c91f3caaefd01a1f71a8e81c7
Registration Date: December 30, 2021

Manufacturer

Name: DRGEM CORPORATION

Authorized Representative

Name: FUJIFILM MYANMAR LIMITED

About this record

Access comprehensive regulatory information for Diagnostic X-ray System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7806ce9c91f3caaefd01a1f71a8e81c7 and manufactured by DRGEM CORPORATION. The device was registered on December 30, 2021.

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.