Myanmar FDA registration 7de802653f20d372a8aa646563966c82

Endoscopic CO₂ Regulator

Myanmar·FUJIFILM·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered September 12, 2022

Device classification

Brand Name: FUJIFILM

Registration information

Analysis ID: 7de802653f20d372a8aa646563966c82
Registration Date: September 12, 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 CO₂ Regulator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7de802653f20d372a8aa646563966c82 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on September 12, 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.