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ADVIAยฎ 2120i Hematology Systems - SFDA Registration ME0000004050SFDAA00025

Access comprehensive regulatory information for ADVIAยฎ 2120i Hematology Systems 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 ME0000004050SFDAA00025 and manufactured by Siemens Healthcare Diagnostics Inc..

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)
ME0000004050SFDAA00025
ADVIAยฎ 2120i Hematology Systems
SFDA Registration: ME0000004050SFDAA00025
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Product Information

Automated hematology analyzers

Product Use

The ADVIAยฎ 2120 and ADVIAยฎ 2120i with autoslide are quantitative, automated hematology analyzers that provide information for in vitro diagnostic use in clinical laboratories.

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000004050SFDAA00025
Authorization ID
MDMA-1-2019-2271
Status
Active
Expire Date
May 27, 2027
Manufacturer
Model Information
Model ID(s)
11219531 11219530 11219529
Product Accessories

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