Saudi Arabia SFDA registration ME0000000626SFDAA00091
EG-530CT
Saudi Arabia·MD·FUJIFILM Corporation·Class IIaActiveProduct information
Medical Endoscope for the upper digestive tract
Product use
This product is a medical Endoscope for the upper digestive tract. It is intended for observation, diagnosis, and endoscopic treatment of the esophagus, stomach, and duodenal bulb at medical facilities under management of physicians. Never use this product for any other purposes
Device classification
- Risk Class
- Class IIa
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000000626SFDAA00091
- Authorization ID
- MDMA-1-2019-2645
- Status
- Active
- Expire Date
- May 26, 2024
Manufacturer
- Manufacturer Name
- FUJIFILM Corporation
Model information
- Model ID(s)
- EG-530CT
Product accessories
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About this record
Access comprehensive regulatory information for EG-530CT in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000000626SFDAA00091 and manufactured by FUJIFILM Corporation.
This page provides complete registration details including product category (MD), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
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