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FOBIT FW III - SFDA Registration ME0000000626SFDAA00126

Access comprehensive regulatory information for FOBIT FW III in the Saudi Arabia medical device market through Pure Global AI's free database. This General IVD(Others) device is registered with Saudi Arabia SFDA under registration number ME0000000626SFDAA00126 and manufactured by FUJIFILM Corporation.

This page provides complete registration details including product category (Chemicals), 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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General IVD(Others)
ME0000000626SFDAA00126
FOBIT FW III
SFDA Registration: ME0000000626SFDAA00126
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Product Information

Fecal Occult Blood Analyzer

Product Use

Analyze stool sample result positive or negative

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000000626SFDAA00126
Authorization ID
GHTF-2019-3875
Status
Active
Expire Date
May 21, 2022
Manufacturer
Manufacturer Name
FUJIFILM Corporation
Model Information
Model ID(s)
16634360
Product Accessories

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