Myanmar FDA registration 78132e3e208f645f5a95cb555fef081b

Clinical Chemistry Analyzer (FUJI DRI-CHEM NX600)

Myanmar·FUJIFILM·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered December 02, 2022

Device classification

Brand Name: FUJIFILM

Registration information

Analysis ID: 78132e3e208f645f5a95cb555fef081b
Registration Date: December 02, 2022

Manufacturer

Name: FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office

Authorized Representative

Name: ADVANCED MEDICAL & DIAGNOSTICS TRADING LIMITED

About this record

Access comprehensive regulatory information for Clinical Chemistry Analyzer (FUJI DRI-CHEM NX600) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 78132e3e208f645f5a95cb555fef081b and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on December 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.