Aids in the detection of Influenza types A and B, including H1N1 strain.
Qualitative detection with results in as little as three minutes.
Suitable samples include Nasal Swabs, Nasal Aspirate, and Throat Swabs.
High Sensitivity (90%) and Specificity (96%) for Flu A and B, when compared to cell culture.

Intended Use
One Step hCG Pregnancy Test is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in urine, as an aid for the early detection of pregnancy.
 
PERFORMANCE CHARATERISTICS
Sensitivity: hCG Pregnancy Test detects hCG concentration of 25 mIU/ml and greater. The test has been standardized to the World Health Organization Third International Standard.
 
Specificity:The addition of LH (300 mIU/ml), FSH (1000 mIU/ml), and TSH ( 1000 mIU/ml) to negative (0 mIU/ml HCG) and positive (25 mIU/ml hCG) specimens showed no cross-reactivity.
 
Accuracy: more than 99%.

Intended Use
One Step hCG Pregnancy Test is a rapid chromatographic immunoassay for the qualitative detection of human chorionic gonadotropin (hCG) in urine, as an aid for the early detection of pregnancy.
 
PERFORMANCE CHARATERISTICS
Sensitivity: hCG Pregnancy Test detects hCG concentration of 25 mIU/ml and greater. The test has been standardized to the World Health Organization Third International Standard.
 
Specificity:The addition of LH (300 mIU/ml), FSH (1000 mIU/ml), and TSH ( 1000 mIU/ml) to negative (0 mIU/ml HCG) and positive (25 mIU/ml hCG) specimens showed no cross-reactivity.
 
Accuracy: more than 99%.

INTENDED USE
Rapid Malaria(p.f.)Test is A Colloidal Gold Enhanced, Rapid Immunochromatographic Assay for testing, in vitro , the presence of Plasmodium falciparum malaria in blood. The test is an antigen-capture assay detecting presence of a specific soluble protein, histidine-rich protein II (PfHRP-II), which is present in, and released from, infected red blood cells.The assay is intended for use with whole blood and does not require additional instruments.
 
PERFORMANCE CHARACTERISTICS
The following data was generated by from previously frozen whole blood samples, and was determined by correlation to standard thick and thin smear microscopic examination with discrepants evaluated via PCR. Retrospective study results are summarized below:
Site                    Pos Neg Test Pos Test Neg
India                     66 86 64(97%) 86(100%)
Senegal                 8 10 8(100%) 10(100%)
Varied Origin       48 53 46(95.8%) 53(100%)
South Africa        102 150 99(97%) 149(99.3%)
TOTAL                  224 299 217(96.9%) 298(99.7%)

The Malaria Test did not cross-react with any of the following species of malaria:

P.malariae, P.ovale, and P.vivax
 

INTENDED USE
Rapid Malaria(p.f.)Test is A Colloidal Gold Enhanced, Rapid Immunochromatographic Assay for testing, in vitro , the presence of Plasmodium falciparum malaria in blood. The test is an antigen-capture assay detecting presence of a specific soluble protein, histidine-rich protein II (PfHRP-II), which is present in, and released from, infected red blood cells.The assay is intended for use with whole blood and does not require additional instruments.
 
PERFORMANCE CHARACTERISTICS
The following data was generated by from previously frozen whole blood samples, and was determined by correlation to standard thick and thin smear microscopic examination with discrepants evaluated via PCR. Retrospective study results are summarized below:
Site                    Pos Neg Test Pos Test Neg
India                     66 86 64(97%) 86(100%)
Senegal                 8 10 8(100%) 10(100%)
Varied Origin       48 53 46(95.8%) 53(100%)
South Africa        102 150 99(97%) 149(99.3%)
TOTAL                  224 299 217(96.9%) 298(99.7%)

The Malaria Test did not cross-react with any of the following species of malaria:

P.malariae, P.ovale, and P.vivax
 

Intended Use
Urinalysis Reagent Strips provide tests for Glucose, Bilirubin, Ketone (Acetoacetic Acid), Specific Gravity, Blood, pH, Protein, Urobilinogen, Nitrite, Leukocytes and Ascorbic Acid in urine. Test results may provide information regarding the status of carbohydrate metabolism, kidney and liver function, acid-base balance and bacterium.

 Technical Specifications.
The following table lists the generally detectable levels of analysis in contrived urine with Urine Reagent Strips 11 parameters: Item Sensitivity Instrumental Visual Test Range Test Range Glucose (mmol/L)2.8 - 5.5 Neg. –55 Neg. – 55 Protein (g/L) 0.15 – 0.3 Neg. –3.0 Neg. – 20.0 Ketone (mmol/L) 0.5 – 1.0 Neg. – 7.8 Neg. – 16 Blood (Ery/ul) 5 – 15 Neg. – 200 Neg. - 200 Bilirubin (μmol/L) 3.3 – 8.6 Neg. – 100 Neg. – 100 Nitrite (μmol/L) 13 – 22 Neg. or pos. Neg. or pos. Leukocytes (cells/μl) 5 – 15 Neg. – 500 Neg. – 500 Urobilinogen (μmol/L)3.3 – 16 3.3 – 131 3.3 – 131 Ascorbic acid (mmol/L)0.3-0.6 0 - 5.0 0 - 5.0 PH --- 5.0 – 9.0 5.0 – 8.5 Specific Gravity --- 1.005 – 1.030 1.000– 1.030

Intended Use
Urinalysis Reagent Strips provide tests for Glucose, Bilirubin, Ketone (Acetoacetic Acid), Specific Gravity, Blood, pH, Protein, Urobilinogen, Nitrite, Leukocytes and Ascorbic Acid in urine. Test results may provide information regarding the status of carbohydrate metabolism, kidney and liver function, acid-base balance and bacterium.

 Technical Specifications.
The following table lists the generally detectable levels of analysis in contrived urine with Urine Reagent Strips 11 parameters: Item Sensitivity Instrumental Visual Test Range Test Range Glucose (mmol/L)2.8 - 5.5 Neg. –55 Neg. – 55 Protein (g/L) 0.15 – 0.3 Neg. –3.0 Neg. – 20.0 Ketone (mmol/L) 0.5 – 1.0 Neg. – 7.8 Neg. – 16 Blood (Ery/ul) 5 – 15 Neg. – 200 Neg. - 200 Bilirubin (μmol/L) 3.3 – 8.6 Neg. – 100 Neg. – 100 Nitrite (μmol/L) 13 – 22 Neg. or pos. Neg. or pos. Leukocytes (cells/μl) 5 – 15 Neg. – 500 Neg. – 500 Urobilinogen (μmol/L)3.3 – 16 3.3 – 131 3.3 – 131 Ascorbic acid (mmol/L)0.3-0.6 0 - 5.0 0 - 5.0 PH --- 5.0 – 9.0 5.0 – 8.5 Specific Gravity --- 1.005 – 1.030 1.000– 1.030