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DxI 9000 Access Immunoassay Analyzer - SFDA Registration ME0000014865SFDAA00035

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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A
ME0000014865SFDAA00035
DxI 9000 Access Immunoassay Analyzer
SFDA Registration: ME0000014865SFDAA00035
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Product 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

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