Antigen tests are used in the diagnosis of respiratory pathogens and are immunoassays that detect the presence of a specific viral antigen, which implies current viral infection. COVID-19 Antigen Rapid Test is designed to detect the presence of viral proteins (antigens) expressed by the COVID-19 virus in a sample from the respiratory tract of a person and is gives results in a few minutes whether someone is infectious. Approved by clinical specimens and authorities, this product is intended exclusively for professional use in the laboratory and at the point-of-care. .
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Flowflex self-test 5 pieces / pack
380 000 pcs single package SELF-TEST 1pcs KIT Goldsite CE1434 LAIENTEST NASAL Price start from 1.79 IFU inside EN / DE / PL BOX PL / EN / DE Optional PDF IFU FR / IT / ES / DA Our warehouse in Poland! We are authorized distributor
1 test *500BOX/CTN home self test kit MOQ 2000
25tests*40box/ctn professional antigen test kit by nasal swab carton size : PEI BFARM CE certificate 53.5*50*34CM GW:16KG
RAPID SARS-CoV-2 antigen test card
Nasal and antibody covid 19 test kit
Covid Test Kit -19 FDA approved
FDA Approved Covid anti body test kit
Covid test kit, FDA approved
Covid test kit
Multi-drug One Step 2-15 Urine Drug Test Cup (MOP, MET, KET, AMP, BAR, BUP, BZO, COC, COT, MDMA, THC, MTD, OPI, PCP, TCA)
A rapid, one step test for the qualitative detection of Amphetamines in human urine. For healthcare professionals including professionals at point of care sites For professional in vitro diagnostic use only. A drug-free urine pool was spiked with Amphetamine at the following concentrations: 0 ng/mL, 500 ng/mL, 750 ng/mL, 1,000 ng/mL, 1,250 ng/mL and 1,500 ng/mL. The result demonstrates >99% accuracy at 50% above and 50% below the cut-off concentration. The data are summarized below: AMP Concentration (ng/mL)Percent of CutoffnVisual Result NegativePositive 00%30300 500-50%30300 750-25%30237 1,000Cutoff30921 1,250+25%30129 1,500+50%30030
Lateral Test and Seal Packers Logiball 2001L packers are used to test and seal off infiltration in sewer laterals, from the mainline, without any access to cleanouts. The lateral grouting plug is inverted and deployed into the lateral from the mainline packer assembly. The mainline sleeve then expands to create a minimal grout mixing chamber. The grout is pumped and migrates freely along the restricted expansion of the lateral plug and out through existing pipe defects into the surrounding bedding to seals defects, leaving only a thin layer of grout in the lateral. The packers are available with different void pressure monitoring systems; a conventional localized liquid filled sensor (S), recommended for acrylamide and acrylate grouts, an in-wall water chamber sensor (W), recommended for stickier grouts such as urethanes and polyurethanes, or both systems (S+W) for a more versatile use. The 2001L Lateral Packer comes standard with two grout ports and a third port dedicated for the test medium (air or water). 2001L Lateral packers work best with a five-hose system. Lateral Grouting Plugs can be interchanged in a matter of minutes to grout distances up to 30 feet if necessary. Lateral Grouting Plugs are available for 4, 5 or 6 diameter laterals. Flexible housing extensions are needed for lateral grouting plugs 24 or longer. ICGA promotes the proper use of chemical grouting as a safe, economical and effective means to reduce ground water infiltration into sewer collection systems. The 2001L model is available for 6â?³, 8â?³, 9â?³, 10â?³, 12â?³, 15â?³, 18â?³, 21â?³, 24â?³ and 30â?³ mainlines. For larger diameter contact our sales department. For larger diameters, see our Man Entry Lateral Packers for 36â??â?? & up or contact our sales department. Features * As measured on the rubber. Specifications subject to change without notice. Logiball Lateral Packer Approximate Void Volumes. View list of parts for the lateral packers 2001L. (pdf file) A Control Panel is available to operate the lateral packer from the truck.
The Treponema pallidum Antibody Assay Kit (Colloidal Gold) is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG, IgM and IgA) to Treponema pallidum (Tp) in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with Tp.
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The test is a rapid colloidal gold immunochromatographic assay for the in vitro qualitative detection of the novel coronavirus(SARS-CoV-2), the influenza A virus (FluA) and the influenza B(FluB) antigen in human nasopharyngeal swab, oropharyngeal swab, nasal swab, and saliva samples from individuals suspected of respiratory viral infection.
The kit is intended for the in vitro qualitative determination of Novel Coronavirus (2019-nCoV) IgG/IgM antibody in human serum, plasma or whole blood. Testing is limited to supplementary detection indicator for suspected nucleic acid negative results or in conjunction with nucleic acid detection in the diagnosis of suspected cases. It should not be used as the basis for diagnosis and exclusion of Novel Coronavirus Pneumonia.
The kit is used to qualitatively detect the novel coronavirus (SARS-CoV-2) nucleocapsid protein antigen in human nasal swab samples in vitro. In the acute phase of infection, antigens are usually detectable in upper respiratory tract specimens.
