Saudi Arabia SFDA registration ME0000004050SFDAA00025
ADVIA® 2120i Hematology Systems
Saudi Arabia·Chemicals·Siemens Healthcare Diagnostics Inc.·General IVD(Others)ActiveProduct information
Automated hematology analyzers
Product use
The ADVIA® 2120 and ADVIA® 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
- Manufacturer Name
- Siemens Healthcare Diagnostics Inc.
Model information
- Model ID(s)
- 11219531 11219530 11219529
Product accessories
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About this record
Access comprehensive regulatory information for ADVIA® 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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