Made in Canada Health Canada approved CE Mark and ISO certified The product has proven to have 100% Specificity and 96% Sensitivety Stock availabity: 2 Million tests/kit in Canada Production: up to 5 Million tests/kit weekly The Rapid Response COVID-19 Antigen Rapid Test Device is an in vitro immunochromatographic assay for the direct and qualitative detection of SARS-CoV-2 viral nucleoprotein antigens from nasal and nasopharyngeal secretions from individuals suspected of COVID-19 within 6 days of symptom onset. This test is authorized for use at the Point of Care i.e., in patient care setting. Results are for the identification of SARS-CoV-2 viral nucleoprotein antigen. Antigen is generally detectable in nasopharyngeal and nasal secretions during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease. Laboratories are required to report all positive results to the appropriate public health authorities. Negative results should be treated as presumptive, and do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patientâ??s recent exposures, history, and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management. The Rapid Responseâ?¢ COVID-19 Antigen Rapid Test Device is for use at the Point of Care for professional use only. PRODUCT INFORMATION: Product: Rapid Respose Sample: Nasal / Nasopharyngeal secretions Format: Cassette Quantity: 25 Tests/Kit per box Time to result: 15 minutes Storage Condition: 2-30 C/36-86 F Test Principle: Immunochromatographic Assay CONTENTS - Individually packed test devices Extraction Buffer Extraction tube Nozzle with filter Tube stand Individually packed swabs Package Insert
Rapid Antigen Covid-19Test Kits 200 million boxes - $3 per test Health Canada, IVD, TUV, CE certification Product Information: Quantity: 20 tests/kit Sample type: Nasopharyngeal swab Storage temperature: 2-30°C The most accurate rapid antigen tests worldwide and provide results in 10 minutes. Test time: 10-15 minutes Rapid 2019-nCoV IgG/IgM Combo Test is a rapid immunochromatographic assay for the simultaneous detection of IgG and IgM antibodies to 2019 novel coronavirus (2019-nCoV, SARS-CoV-2) in human serum, plasma, or whole blood. Kit Contains: 20 Rapid SARS-CoV-2 Antigen Test Cards (Individually packaged) 2 Sample Buffers 20 Sterilized swabs (Individually packaged) 20 Extraction tubes (Individually packaged) 1 Instructions for use 1 Tube rack (for 6 tubes/rack)
1. Generic Name: Novel Coronavirus COVID-19 IgG Antigen Test Kit 2. Brand Name: NIL 3. Notified Category: Other than above substances intended for qualitative determination of COVID-19 infection 4. Class of Medical Device: Class D 5. Shelf life :15 months 6. Sterile/Non-Sterile: Non-Sterilized 7. Contains Drugs: No 8. Medical Device Grouping Category: IVD-Kit 9. Grouping Description: Intended for qualitative determination of COVID-19 infection 10. Intended Use: The Novel Coronavirus COVID-19 IgG Kit is intended for the qualitative detection of human anti-COVID- 19 IgG antibody in human serum/plasma. Any reactive specimen with the Novel Coronavirus COVID-19 IgG Kit must be confirmed with alternative testing method(s). 11. Product Description: Assay controls and 1:10 diluted human serum samples are added to the microtiter wells of a microplate that was coated with COVID-19 recombinant full length recombinant protein. After the first incubation period, the unbound protein matrix is removed with a subsequent washing step. A horseradish peroxidase (HRP) labeled polyclonal goat anti-human IgG tracer antibody is added to each well. After an incubation period, an immunocomplex of "COVID-19 recombinant antigen-human anti-COVID-19 IgG antibody - HRP labeled anti human IgG tracer antibody" is formed if there is specific Coronavirus IgG antibody present in the tested specimen. The unbound tracer antibody is removed by the subsequent washing step. HRP-Labeled tracer antibody bound to the well is then incubated with a substrate solution in a timed reaction and then measured in a spectrophotometric microplate reader. The enzymatic activity of the tracer antibody bound to the anti-COVID-19 IgG on the wall of the microtiter well is proportional to the amount of the anti-COVID-19 IgG antibody level in the tested specimen. SALIENT FEATURES: â?¢ Recombinant COVID-19 Spike subunit Protein coated on Microwell Plate â?¢ HRP Conjugated Polyvalent Anti-Human IgG â?¢ Assay Time: 80 mins (30mins+30 Mins+20mins) â?¢ Strip Format Microwell Plate â?¢ Ready to use Substrate and Controls â?¢ Only 20 pL of human serum is required for measurement in duplicate. â?¢ Works on any open ELISA system â?¢ Assay procedure is easy to automate OUR TEST: â?¢ Principle: Indirect ELISA â?¢ The normal healthy patients with samples collected prior to the COVID-19 outbreak [December 3, 2019] (n = 150) and RT-PCR confirmed positive patients in after the second week of the onset of the disease (n = 32). The Positive sample evaluation was done at external Approved Lab. The results are as follows: â?¢ Diagnostic sensitivity is 100% (>98%) â?¢ Diagnostic specificity is 98.67% (>97%) â?¢ PPV: 94.12�°/0 â?¢ NPV: 100% Please contact us for more information and product details.
Specification Product Name VivaDiag SARS-CoV-2 IgM/IgG Rapid Test (COVID-19 IgM/IgG Rapid Test) Test Principle Colloidal gold Sample Type Whole blood (fingertip/venous ), serum or plasma Sample Volume 10 �¼L Test Time 15 min Operation Temperature 15-30 Storage Temperature 2-30 Shelf Life (Unopened) 24 months
- Abbott Nasal POC - Abbott Nasopharyngeal POC - Genrui POC - VivaDiag Saliva POC - FaStep Saliva POC
Reagent Test Strip iChem VELOCITY Urinalysis Multiple Analytes For iChem VELOCITY Systems 100 Strips UOM: 100/BX Product Number: 800-7212 Manufacturer: Beckman Coulter
Reagent Cobas Liat Nucleic Acid Test Influenza A / B, Respiratory Syncytial Virus (RSV) For Cobas Liat Automated PCR Analyzer 20 Tests 20 Tubes UOM: 20/CS Product Number: 08160104190 Manufacturer: Roche
Blood sample size: 1-2 µL; if sample applied at the center of test pad. Sample type: Capillary, Venous, Arterial, Neonatal. Sample dosing: Large test pad for top dosing suitable for AST options. Compatibility: Only with AC Active meter. Storage: +2C to 30C. Quality control: 2 levels - 50 mg/dL and 150 mg/dL. Strip Stability: 18 months
New Sealed in Box FreeStyle Lite 50ct Test Strips Expire 02/2024
New Sealed in Box FreeStyle Lite 100ct Test Strips Expire 02/2024
New Sealed in Box OneTouch Ultra Blue 50ct Test Strips Expiration: 10/2023
Covi-G (powered by Cipla) Rapid Test kit combines quality, efficacy and convenience - offering precise results in 10-15 mins Features & Benefits Covid IgM-IgG Serologic Rapid Test for COVID-19 is used to qualitatively detect IgG and IgM antibodies against SARS-CoV-2 in whole blood in vitro Precise and effective - Tests for both IgM and IgG antibodies - Sensitivity and specificity comparable to highest available offerings Sensitivity: IgG 92%, IgM 82%; Specificity IgG 97%, IgM 94% - ->92% total accuracy: IgG 96,5% - IgM: 92,8% - High reproducibility (consistent results across the same patient) - High quality, reliable & convenient - Single-prick blood test - 10-15 minutes per test - Intuitive visual interpretation - No specialized training or equipment needed - Portable hence highly scalable - Storage at room temperature (2-30 C) - Conformance to CE (Europe) and ISO manufacturing The Covi-G platform for Rapid Antibody tests has a set of unique and unparalleled offerings SUSTAINABLE QUALITY Validated Declaration of CE conformity - Launched in Feb 2020, among the earliest technologies/ kits to declare CE-compliance, and continuing strong compared to competitors - Under process for receiving USDA E authorization Among only 3 integrated vendors of Rapid tests Developed and manufactured in Europe (Belgium) - One of the very lew players manufacturing in Europe, with zero complaints also certified locations ACCEPTABILITY ACROSS MARKETS Demonstrated capabilities in local countries validation - Independent local studies conducted in Belgium and France, validating the sensitivity and specificity of the product Participated in published research - Covl-G kit compared lavorably with 7 lgFL IgM rapid antibody tests and IgG ELISA in a comparative study published by Elsevier Science Direct, verifying sensitivity of the kit PROVEN COMMERCIAL EXPERIENCE Sold in 25+ countries already - Including Europe, US, Canada, Africa and multiple developed and emerging markets - Under participation in govt tenders Robust manufacturing capability and capacity - ISO-certified manufacturing site - Ability to cater to high manufacturing volumes from Belgium, to ensure adequale QA and commercial viability AFFORDABLE AND SCALABLE Viable to scale up at Institutions and Retail level - Economical cost per-unit established over many months of process improvement and local manufacturing - Can cater to insured as well as out-of pocket populations Continuous improvement through R&D - Multiple rounds of performance testing complete, further testing in 5 reputed hospitals underway in Belgium, France, USA and Canada - Other platforms including Rapid antigen testing also being developed The price is per unit, the minimum is 25000 units
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 test shows the presence in blood or serum of HIV antibodies (both type 1 and type 2).
Product Description FDA EUA, CE Price of product ( USD price or FOB price) : "10,000-99,999: $8.45 100,000-249,999:$7.98 250,000-499,999: $7.78 500,000+: Contact" Product origin : China Minimum Order Size and Packgaing details : 10,000 Individual tests (25/box)
Test kits for covid-19 We have testing kits for Covid-19 In inventory now for immediate shipping. High sensitivity rapid test kits for Covid-19. 250K available now for USA and international shipping, Inventory moving fast.
The COVID-19 IgG/IgM (Whole Blood/Serum/Plasma) Rapid Test Device utilizes lateral flow technology that is used for the qualitative, differential detection of both anti-SARS-CoV-2 IgM and IgG antibodies. In general, antibodies can be detected 1-3 weeks after infection. This test is intended to screen patients for COVID-19. Combining RNA and Antibody tests can significantly raise the sensitivity for detecting COVID-19 in infected individuals. This test has been authorized by the FDA under a EUA for professional use CLIA and CLIA WAIVED for Point Of Care. This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens. This product is intended for professional use and not for home use. FACT SHEET FOR HEALTHCARE PROVIDERS This test has been authorized by the FDA under a EUA for use by authorized CLIA laboratories. This device is CLIA waived for point of care use for fingerstick whole blood specimens only. The user should be trained in the procedure. Wear appropriate protective attire for your safety when handling patient samples. This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens. There should be a blue line in the control region (next to ) before testing, discard the device if there is no blue line.
Highest accuracy Fast result interpretation Cost effective Made with best choices of materials Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Accuracy: 99.9% Sensitivity: 20 miu/ml Specimen: urine .
Highest accuracy Fast result interpretation Cost effective Made with best choices of materials Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Accuracy: 99.9% Sensitivity: 20 miu/ml Specimen: urine .
Highest accuracy Fast result interpretation Cost effective Made with best choices of materials Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Sensitivity: 94.3% Specificity: >98.9% Specimen: whole blood/serum/plasma .
