95.6% Sensitivity Rapid Test Device Nasopharyngeal Swab Lollipop
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95.6% Sensitivity Rapid Test Device Nasopharyngeal Swab Lollipop
Product Description Factory price high sensitivity Covid 19 Ag saliva rapid test kit
(lollipop) COVID-19 Ag Rapid Saliva Test Device is a rapid
chromatographicimmunoassay for the qualitative detection of N
antigen from SARS-CoV-2 present in human saliva within the first 7
days of symptom onset. This test is for professional used only, as
an aid toearly diagnosis of SARS-CoV-2 infection in patient.The
result of this test should not be the sole basis for the diagnosis;
confifirmatory testing is required Date sheet
Directions for Use 1) Remove the test device from the sealed pouch and use the device
as soon as possible. Best results will be obtained if the assay is
performed immediately after opening the foil pouch. 2) Cough deeply twice before collecting the samples. 3) Pull the blue cap off gently by holding the sides to expose the
collection pad. 4) Hold the top portion of the device and place the collection pad
into the mouth. 5) Rub the collection pad against the cheek and tongue gently in a
circular motion about 10 times. And then place the collection pad
in the mouth for about 1~2 minutes until the C line show up in the
C region. 6) Remove the device from mouth as soon as the C line appears at
the C region. 7) Place the cap onto the device, lay it on a flat surface. 8) Read results at 10-15minutes after removing device from mouth. Do not read results after 20 minutes. Interpretation of Results NEGATIVE: Only one red band appears in the control region (C), and no band
in the test region (T). The negative result indicates that
there are no Novel coronavirus antigen in the sample or the number
of viral particles is below the detectable range. POSITIVE: Two red bands appear. One red band appears in the control region
(C), and one red band in the test region (T). The shade of color
may vary,but it should be considered positive whenever there is
even a faint band. INVALID: No red band appears in the control region (C). The test is invalid
even if there is a band on test region (T). Insufficient sample
volume or incorrect procedural techniques are the most likely
reasons for control line failure. Review the test procedure and
repeat the test using a new test device Company Information Innovation Biotech (Beijing) Co., Ltd. is a biotechnology company specializing in research, development and manufacturing of advanced medical in-vitro diagnostic (IVD) rapid test kits, medical and laboratory disposal products. We provide one step medical diagnostic rapid test kit based on our INVBIO brand, Product include Fertility Tests, Tumor markers, DOA drug of abuse test, Drug test cup, Urinalysis reagent strip, ELISA kit, Digital alcohol tester, urine analyzer, et. OEM packaging is available, drug of abuse test, troponin I test, alcohol screening saliva test strips, urine strips, elisa kits, microscope slides Our focus is to expand our markets internationally by forming strategic alliances and entering into partnerships with distributors worldwide. We have established an international reputation for excellence in the manufacturing of quality medical and laboratory products. In addition, we have obtained approval licenses ISO13485, FSC certificate, and most of our products get CE mark Our objective is the utmost satisfaction of our clients all around the world by supplying our quality and economical products
Certifications
Contact information Mob/WhatsApp/WeChat/Skype: 008618579609735 Website: www.invbio.com
FAQ Q: What is your payment terms? A: Payment terms: 100% TT before shipment Q: Can you send samples? A: Yes,SAMPLES can be sent for your evaluation.customer pay the freight charge Q: Do you give any discount? |
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