Saudi Arabia SFDA registration ME0000014865SFDAA00035
DxI 9000 Access Immunoassay Analyzer
Saudi Arabia·Beckman Coulter, Inc.·AActiveProduct information
used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids.
Device classification
- Risk Class
- A
- Product Type
- IVD
Registration information
- Registration ID
- ME0000014865SFDAA00035
- Authorization ID
- MDMA-2-2023-0548
- Status
- Active
- Expire Date
- April 13, 2026
Manufacturer
- Manufacturer Name
- Beckman Coulter, Inc.
Model information
- Model ID(s)
- ME0000014865SFDAA00035
Product accessories
[]
About this record
Access comprehensive regulatory information for DxI 9000 Access Immunoassay Analyzer in the Saudi Arabia medical device market through Pure Global AI's free database. This A device is registered with Saudi Arabia SFDA under registration number ME0000014865SFDAA00035 and manufactured by Beckman Coulter, Inc..
This page provides complete registration details including 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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