Myanmar FDA registration 1d9d3537c58a94c149e7f0ebfa6d05e3
Gastroenterology Endoscopy System
Myanmar·FUJIFILM·FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office·Registered July 07, 2022Device classification
- Brand Name
- FUJIFILM
Registration information
- Analysis ID
- 1d9d3537c58a94c149e7f0ebfa6d05e3
- Registration Date
- July 07, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Gastroenterology Endoscopy System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1d9d3537c58a94c149e7f0ebfa6d05e3 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on July 07, 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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