Saudi Arabia SFDA registration ME0000004050SFDAA00036
ADVIA® 360 Lyse 3P Diff
Product information
Reagent for differentiation of leucocyte
subpopulations."
Product use
Reagent for differentiation of leucocyte subpopulations for the ADVIA® 360 Hematology system.
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000004050SFDAA00036
- 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)
- 11170848
Product accessories
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About this record
Access comprehensive regulatory information for ADVIA® 360 Lyse 3P Diff 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 ME0000004050SFDAA00036 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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