Saudi Arabia SFDA registration ME0000004050SFDAA00034
ADVIA 120, ADVIA 2120, ADVIA 2120i PEROX SHEATH
Saudi Arabia·Chemicals·Siemens Healthcare Diagnostics Inc.·General IVD(Others)ActiveProduct information
For quantitative determination of white blood cells
Product use
"For in vitro diagnostic use in the quantitative determination of white blood cells and subpopulations in blood on ADVIA® 120/2120/2120i Hematology systems.
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Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000004050SFDAA00034
- 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)
- 03624240
Product accessories
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About this record
Access comprehensive regulatory information for ADVIA 120, ADVIA 2120, ADVIA 2120i PEROX SHEATH 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 ME0000004050SFDAA00034 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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