Myanmar FDA registration 46ac5bb5ae5d6d89c3d4eb442fbdfb34

Clinical Chemistry Analyzer

Myanmar·FUJIFILM·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered March 25, 2022

Device classification

Brand Name: FUJIFILM

Registration information

Analysis ID: 46ac5bb5ae5d6d89c3d4eb442fbdfb34
Registration Date: March 25, 2022

Manufacturer

Name: FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office

Authorized Representative

Name: FUJIFILM MYANMAR LIMITED

About this record

Access comprehensive regulatory information for Clinical Chemistry Analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 46ac5bb5ae5d6d89c3d4eb442fbdfb34 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on March 25, 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.