Upper and Lower Gastrointestinal Endoscope - FDA Registration f72afc612aea47386040b733d26dbadf
Access comprehensive regulatory information for Upper and Lower Gastrointestinal Endoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f72afc612aea47386040b733d26dbadf and manufactured by FUJIFILM Healthcare Manufacturing Coroporation Sano Office. The device was registered on September 27, 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.
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FDA Official Data
f72afc612aea47386040b733d26dbadf
Upper and Lower Gastrointestinal Endoscope
FDA ID: f72afc612aea47386040b733d26dbadf
Device Classification
Brand Name
FUJIFILM
Registration Information
Analysis ID
f72afc612aea47386040b733d26dbadf
Registration Date
September 27, 2022
Manufacturer
Authorized Representative

