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Influenza A+B Rapid Test Uncut Sheet Nasopharyngeal Swab Rtk

Hangzhou Aichek Medical Technology Co.,Ltd
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Hangzhou Aichek Medical Technology Co.,Ltd

Influenza A+B Rapid Test Uncut Sheet Nasopharyngeal Swab Rtk

Country/Region china
City & Province hangzhou zhejiang
Categories Cotton Pad
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Product Details

Infection Disease Influenza A+B Antigen Rapid Test with CE certificate uncut sheet

 

Product Name 

Influenza A+B Antigen Rapid Test uncut sheet

Formats

Strip(3mm)Device(4mm) uncut sheet

Place of Origen

China

Specimen

swab

Read Time

15 minutes

Shelf life

2 years

Package

25 device/box or 50 strip/Box

Storage

2℃-30℃

 
For professional in vitro diagnostic use only
 

【INTENDED USE】

 

The Influenza A+B Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of influenza A and B antigens in nasal swab or throat swab or nasal aspirate specimens. It is intended to aid in the rapid differential diagnosis of influenza A and B viral infections.

 

 

PRINCIPLE

 

The Influenza A+B Rapid Test Device (Swab/Nasal Aspirate) is a qualitative, lateral flow immunoassay for the detection of Influenza A and Influenza B nucleoproteins in nasal swab, throat swab or nasal aspirate specimens. In this test, antibody specific to the Influenza A and Influenza B nucleoproteins is separately coated on the test line regions of the test Device. During testing, the extracted specimen reacts with the antibody to Influenza A and/or Influenza B that are coated onto particles. The mixture migrates up the membrane to react with the antibody to Influenza A and/or Influenza B on the membrane and generate one or two colored lines in the test regions. The presence of this colored line in either or both of the test regions indicates a positive result. To serve as a procedural control, a colored line will always appear in the control region if the test has performed properly

 

Sensitivity, Specificity and Accuracy

 

The Influenza A+B Rapid Test Device (Swab/Nasal Aspirate) has been evaluated with specimens obtained from the patients. RT-PCR is used as the reference method for the Influenza A+B Rapid Test Device (Swab/Nasal Aspirate). Specimens were considered positive if RT-PCR indicated a positive result. Specimens were considered negative if RT-PCR indicated a negative result Nasal Swab Specimen.
 
 Nasal Swab Specimen

 

Type A

Type B

RT-PCR

Total

RT-PCR

Total

Positive

Negative

Positive

Negative

Flu A+B Rapid

Test Strip

Positive

100

2

102

85

2

87

Negative

1

180

181

2

200

202

Total

101

182

283

87

202

289

Relative Sensitivity

99.0%

97.7%

Relative Specificity

98.9%

99.0%

Accuracy

98.9%

98.6%

 
Throat Swab Specimen

 

Type A

Type B

RT-PCR

Total

RT-PCR

Total

Positive

Negative

Positive

Negative

Flu A+B

Rapid Test

Device

Positive

58

1

59

65

1

66

Negative

3

150

153

4

162

166

Total

61

151

212

69

163

232

Relative Sensitivity

95.1%

94.2%

Relative Specificity

99.3%

99.4%

Accuracy

98.1%

97.8%

 
 Nasal Aspirate Specimen

 

Type A

Type B

RT-PCR

Total

RT-PCR

Total

Positive

Negative

Positive

Negative

Flu A+B

Rapid Test

Device

Positive

46

2

48

94

1

95

Negative

0

241

241

2

158

160

Total tal tal

46

243

289

96

159

255

Relative Sensitivity

100%

97.9%

Relative Specificity

99.2%

99.4%

Accuracy

99.3%

98.8%

 

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