FlowFlex Sars-CoV-2 Antigen Rapid Test Self Test - Single Pack
The Flowflex SARS-CoV-2 Antigen Rapid Lateral FlowTest is a lateral flow chromatographic immunoassay for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasal swab specimens directly from individuals who are suspected of an active COVID-19 infection by their healthcare provider within the first seven days of the onset of symptoms.
Supplied in a single pack
Cassette Format
Detects the nucleocapsid protein antigen from SARS-CoV-2
Nasal Specimen sample. Anterior Nares Only Test (2-4cm inside the nostril)
Results in 15 minutes
CE Marked for Self Test
Used by NHS track and trace as home test
Unique ID QR code number on each cassette
Pack Contents
1 x Test Cassette with QR code and unique ID number
1 x Extraction Buffer Tube
1 x Disposable Swab
1 x Waste Bag
1 x Package Insert
Features:
Fully Home Use Approved
FDA Approved
Validation from Public Health England Porton Down.
Full Home Test Approval Granted in the UK & EU
Registered with MHRA and CE Marked.
Used and trusted by companies around the world including all UK airports and the NHS.
First Response Malaria Ag. P.f. / P.v. Card Tests intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum and P. vivax.
Product specifications :
Sensitivity - 100%
Specificity -100%
Rapid Result time within 20 - 30 Minutes.
Detects P. falciparum and P. vivax.
Storage at 1 40C.
Specimen Type- Whole Blood
1708 Rapid Test Kits Suppliers
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CTK biotech, OnSite Chikungunya IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgM anti-chikungunya (CHIK) virus in human serum, plasma or whole blood. CE certified.
CTK Biotech's, OnSite H. pylori Ab Combo Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) against Helicobacter pylori (H. pylori) in human serum, plasma or whole blood.
UNIQUE FEATURES:
EASY TO PERFORM: Rapid, One Step procedure. Test Procedure & interpretation of results printed on individual Pouch
HIGHER SENSITIVITY: Sensitivity of 20 mIU/mL of hCG hormone in Urine ensure the early detection of Pregnancy
FAST & ACCURATE RESULTS: Results within 5 minutes, Positive results just in 30 seconds
BIGGEST TEST WINDOW WIDTH: Test window width of 4mm ensure the clear background and better readability of the test results
USER FRIENDLY: Requires no external measurement system. Can be stored at Room Temperature (2 - 30C).
CAT No : Q-NCOV-01G. STANDARD Q COVID-19 Antigen Test kit is chromatographic immunoassay for the qualitative detection of SARS CoV 2 nucleocapsid antigen present in human nasal sample.
Cat. No : COVAG025-1.The GenBody COVID-19 Ag is an immunochromatographic rapid diagnostic test (RDT) intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) oranteriornasal (AN) swab specimens from individuals who are suspected of COVID-19 by their healthcare provider within the first six days of symptom onset.
CAT No : SS03P25. Sure Status COVID-19 Antigen Card Test is a rapid chromatographic immunoassay for the qualitative detection of specific antigens to SARS-CoV-2 present in human nasopharynx.
CAT No : R0160C. The OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.
Product Description
Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
CTK Biotech's ,
The OnSite Toxo IgG/IgM Combo Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of IgG and IgM anti-Toxoplasma gondii (T. gondii) in human serum, plasma or whole blood.
WHO Approved,
First Response Malaria Antigen P.falciparum (HRP2) Card Test is intended to be performed by trained users (In either laboratory or point of care settings) as qualitative screening in vitro diagnostic test for detection of P. falciparum specific HRP2 antigen.
Sensitivity - 100%
Specificity - 100%
Rapid Result time within 20 - 30 Minutes.
Detects Histidine Rich protein(HRP2) of Plasmodium P.falciparum
Storage at 1 40C.
Specimen Type- Whole Blood
CTK BioTech's '
Designed to specifically detect low levels of fecal occult blood, hHB 25 ng/mL,
Higher accuracy, sensitivity and specificity than the Guaiac Test,
No dietary restrictions,
Clear, easy-to-interpret result,
Individually sealed foil pouches containing:
One cassette test device,,
One desiccant,
Stool collection devices, each containing 2 mL of extraction buffer (REF SB-R2011),
Patient ID stickers,
One package insert (instruction for use).
CTK BioTech's, CE certified, Utilizes recombinant chimeric dengue virus licensed from the US CDC
Detects all four dengue serotypes
Duo test format minimizes processing time
IgM detection indicates recent infection
IgG detection indicates recent or previous infections
Ag detection indicates a current infection
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 �µL Capillary tubes (for Dengue IgG/IgM test)
Plastic droppers (for Dengue Ag test)
Sample diluent (REF SB-R0062, 5 mL/bottle)
One package insert (instruction for use)
CTK BioTech's, CE certified, Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers â?¥70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 �µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patientâ??s visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 µL capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use)
CTK BioTech's, CE certified, Single test for identifying acute infection and protective immunity by detecting and differentiating IgG and IgM anti-HAV
Indicates protective immunity by detecting HAV IgG titers 70 mIU/mL
High confidence as it is traceable to the 2nd WHO International Standard for HAV, and IgM is in agreement with market leading ELISA test: Sensitivity: 94.8%; Specificity: 96.7%
Flexible specimen types including serum, plasma, or whole blood which allows testing at any time without special specimen preparation
Small sample volume (5 µL) enables multiple testing on the same specimen without having to re-draw the patient.
Initial patient care action can begin during the patient's visit as test results are available in 15 minutes.
Easily transported, and can be stored for 24 months at 2-30oC
Individually sealed foil pouches containing:
One cassette device
One desiccant
5 µL capillary tubes
Sample diluent (REF SB-R0092, 5 mL/bottle)
Package insert (instruction for use).
Cat. No : RK033-30. General Description:
STANDARD Q HIV/Syphilis Combo Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies specific to HIV-1 including subtype O, HIV 2 and Syphilis (Treponema pallidum) in human serum, plasma or whole blood. The test is for in vitro diagnostic use and intended as an aid to early diagnosis of HIV and Syphilis infection for HIV or Syphilis infected patients, patients with signs and symptoms (HIV and Syphilis) and persons at risk. The test is able to quick screen the HIV/syphilis infection and gives the advantage of managing these two diseases at the same time.
CAT No : R0160C. The OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood.
Product Description
Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity
Differentiates Between Igg And Igm To Determine Stage Of Infection
One Step Procedure Minimizes Operator Error Due To Sample Preparation
High Level Of Reproducibility
Test Kits Can Be Used And Stored In A Wide Range Of Temperatures
1708 Rapid Test Kits Suppliers
Short on time? Let Rapid Test Kits sellers contact you.
