Saudi Arabia SFDA registration ME0000003094SFDAA00050
LIAISON Toxo IgG II
Saudi Arabia·Chemicals·DiaSorin S.p.A.·Annex II List BActiveProduct information
IVD Kit for determination of specific IgG antibodies to Toxoplasma gondii in human serum or plasma
Product use
The LIAISON® Toxo IgG assay uses chemiluminescent immunoassay (CLIA) technology for the quantitative determination of
specific IgG antibodies to Toxoplasma gondii in human serum or plasma samples for screening of pregnant women.
The test has to be performed on the LIAISON® Analyzer.
Device classification
- Risk Class
- Annex II List B
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000003094SFDAA00050
- Authorization ID
- MDMA-1-2019-4213
- Status
- Active
- Expire Date
- May 26, 2025
Manufacturer
- Manufacturer Name
- DiaSorin S.p.A.
Model information
- Model ID(s)
- 310780
Product accessories
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About this record
Access comprehensive regulatory information for LIAISON Toxo IgG II in the Saudi Arabia medical device market through Pure Global AI's free database. This Annex II List B device is registered with Saudi Arabia SFDA under registration number ME0000003094SFDAA00050 and manufactured by DiaSorin S.p.A..
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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