Saudi Arabia SFDA registration ME0000000626SFDAA00005
Processor
Product information
Processor used in combination with a FUJIFILM medical Endoscope.
Product use
This product is intended to be used in combination with a FUJIFILM or FUJINON
medical Endoscope, light source, monitor, recorder and various peripherals for
observation, diagnosis, endoscopic treatment, and image recording in medical facilities under the management of physicians.
Device classification
- Risk Class
- Class I
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000626SFDAA00005
- Authorization ID
- GHTF-2016-1514
- Status
- Active
- Expire Date
- March 20, 2019
Manufacturer
- Manufacturer Name
- FUJIFILM Corporation
Model information
- Model ID(s)
- VP-4450HD
Product accessories
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About this record
Access comprehensive regulatory information for Processor in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000000626SFDAA00005 and manufactured by FUJIFILM Corporation.
This page provides complete registration details including product category (Medical Device), 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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