Saudi Arabia SFDA registration ME0000001481SFDAA00173
IMMULITE/IMMULITE 1000 Systems sPS Third Generation PSA
Product information
for quantitative measurement of prostate specific antigen in human serum
Product use
for quantitative measurement of prostate specific antigen in human serum used in IMMULITE and immulite 1000 systems
Device classification
- Risk Class
- Annex II List B
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000001481SFDAA00173
- Authorization ID
- GHTF-2019-5843
- Status
- Active
- Expire Date
- December 31, 2019
Manufacturer
- Manufacturer Name
- Siemens Healthcare diagnostics products Limited
Model information
- Model ID(s)
- LKUP1
Product accessories
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About this record
Access comprehensive regulatory information for IMMULITE/IMMULITE 1000 Systems sPS Third Generation PSA 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 ME0000001481SFDAA00173 and manufactured by Siemens Healthcare diagnostics products Limited.
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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