Crp/SAA
Test Strips & Test Tube
Plastic
One Year
Adult
With Logo Printing
ISO, CE
OBM/OEM
Box+Carton
China
Product Description


Intended Use
CRP/SAA Combo Rapid Test Kit(LFIA) is used for the in vitro qualitative detection of C-Reactive Protein/Serum Amyloid A (CRP/SAA) content in human whole blood, plasma and serum.Product Performance
1. Precision
The CRP and SAA positive controls were tested, and the results were all positive.
2.Repeatability
When 10 kits in the same batch detect CRP and SAA precision control samples with concentrations of 200mg/L, 75mg/L and 20mg/L, the results should be consistent, the color rendering should be consistent, and should be all positive.3.Analysis of specificity
The result of detection of CRP and SAA specific quality control products (negative serum or plasma samples) should be negative.
4. The limit of detection
CRP is no higher than 10mg/L, SAA is no higher than 10mg/L.
5. Interfering substances
The samples with hemolysis, hyperlipemia, and jaundice do not interfere with the test results and can be used as testing sample.
6. Clinical results
The rapid detection method and CLIA method were used to detect 1,120 cases of susceptible persons. The comparison of each subject is shown in the following table:
CRP/SAA Combo Rapid Test Kit | CLIA | Total | |
SAA Positive | Negative | ||
SAA Positive | 263 | 5 | 268 |
Negative | 3 | 551 | 554 |
Total | 266 | 556 | 822 |
Sensitivity: 98.1%, specificity: 99.45%, overall consistency: 99.02%




