Saudi Arabia SFDA registration ME0000003094SFDAA00057
LIAISON CMV IgG II
Saudi Arabia·Chemicals·DiaSorin S.p.A.·Annex II List BActiveProduct information
IVD Kit for determination of specific IgG antibodies to hCMV in human serum or plasma
Product use
The LIAISON® CMV IgG II assay uses chemiluminescent immunoassay (CLIA) technology for the quantitative determination of specific IgG antibodies to hCMV in human serum or plasma samples.
The test has to be performed on the LIAISON® analyzer family.
Device classification
- Risk Class
- Annex II List B
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000003094SFDAA00057
- 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)
- 310745
Product accessories
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About this record
Access comprehensive regulatory information for LIAISON CMV 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 ME0000003094SFDAA00057 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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