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Processor - SFDA Registration ME0000000626SFDAA00005

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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Class I
ME0000000626SFDAA00005
Processor
SFDA Registration: ME0000000626SFDAA00005
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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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