Myanmar FDA registration ec0a41efebd15cd9e6960cb02c91e02f
Lower Gastrointestinal Endoscope
Device classification
- Brand Name
- FUJIFILM
Registration information
- Analysis ID
- ec0a41efebd15cd9e6960cb02c91e02f
- Registration Date
- September 22, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Lower Gastrointestinal Endoscope in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ec0a41efebd15cd9e6960cb02c91e02f and manufactured by FUJIFILM Healthcare Manufacturing Coroporation Sano Office. The device was registered on September 22, 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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