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Myanmar FDA registration 1cf9d43a93a2f8cf6231260bf34c52b3

Fibreoptic Bronchoscope System

MyanmarFUJIFILMFUJIFILM Healthcare Manufacturing Corporation Hanamaki OfficeRegistered May 20, 2022
VerifiedFDA Myanmar · official registry
Device classification
Brand Name
FUJIFILM
Registration information
Analysis ID
1cf9d43a93a2f8cf6231260bf34c52b3
Registration Date
May 20, 2022
Manufacturer
Name
FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office
Authorized Representative
Name
SEA LION COMPANY LIMITED
About this record

Access comprehensive regulatory information for Fibreoptic Bronchoscope System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1cf9d43a93a2f8cf6231260bf34c52b3 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on May 20, 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.