Myanmar FDA registration dc8f80b88af961c880e677525471f8d1

Reagent

Myanmar·FUJIFILM·FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office·Registered December 15, 2022

Device classification

Brand Name: FUJIFILM

Registration information

Analysis ID: dc8f80b88af961c880e677525471f8d1
Registration Date: December 15, 2022

Manufacturer

Name: FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office

Authorized Representative

Name: ADVANCED MEDICAL & DIAGNOSTICS TRADING LIMITED

About this record

Access comprehensive regulatory information for Reagent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dc8f80b88af961c880e677525471f8d1 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The device was registered on December 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.