Saudi Arabia SFDA registration ME0000004050SFDAA00033
ADVIA 120, ADVIA 2120, ADVIA 2120i SHEATH RINSE
Saudi Arabia·Chemicals·Siemens Healthcare Diagnostics Inc.·General IVD(Others)ActiveProduct information
Use to operate the Hematology Systems.
Product use
The ADVIA® Hematology Sheath/Rinse reagent is contained in a 20 –liter rectangular container, which is necessary to operate the ADVIA® Hematology Systems.
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000004050SFDAA00033
- 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)
- 02337140 AND 01554628
Product accessories
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About this record
Access comprehensive regulatory information for ADVIA 120, ADVIA 2120, ADVIA 2120i SHEATH RINSE 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 ME0000004050SFDAA00033 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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