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IMMULITE/IMMULITE 1000 systems PSA sample Diluent - SFDA Registration ME0000001481SFDAA00162

Access comprehensive regulatory information for IMMULITE/IMMULITE 1000 systems PSA sample Diluent 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 ME0000001481SFDAA00162 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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Annex II List B
ME0000001481SFDAA00162
IMMULITE/IMMULITE 1000 systems PSA sample Diluent
SFDA Registration: ME0000001481SFDAA00162
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Product Information

For the quantitative measurement of prostate- specific antigen (PSA) in human serum

Product Use

For the manual dilution of patient samples. One vial 25 mL of a PSA-free chicken serum/buffer matrix, with preservative

Device Classification
Risk Class
Annex II List B
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000001481SFDAA00162
Authorization ID
GHTF-2019-6739
Status
Active
Expire Date
October 31, 2019
Manufacturer
Model Information
Model ID(s)
LPSZ
Product Accessories

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