Product Code Product Description PRS-ZE0080 Field Inspection Testing Kit PRS-ZE0082 Field Inspection Pocket Vane Tester PRS-ZE0082/1 Extension Rod for PRS-ZE0082 PRS-ZE0084 Heavy Duty Pocket Penetrometer, 0-10 kgf/cm2 STANDARDS : ASTM D2573 The PRS-ZE0080 Field Inspection Testing Kit is ideal for geotechnicians, geologists and agronomists. It consists of the PRS-ZE0084 Pocket Penetrometer and of the PRS-ZE0082 Field Inspection Pocket Vane Tester. The instrument is contained in a practical carrying case. PRS-ZE0080 Field Inspection Testing Kit Dimensions (packed) 240x210x50 mm Weigth (approx.) 1.8 kg The PRS-ZE0082 Field Inspection Pocket Vane Tester is especially designed to measure the undrained shear strength (CU) of cohesive soils, consists of a cylindrical body with a torsional spring and three interchangeable vanes of different sizes used depending upon the expected strength of the soil. The height/diameter ratio of all vanes is 2. During operation the vane is driven for 5-6 cm into the soil and then turned with the handle. Deep measures (i.e. on the top of undisturbed samples) can be obtained using the extension rod. All stainless steel construction. Supplied in a plastic case. Extension rod should be ordered separately. PRS-ZE0082 Field Inspections Pocket Vane Tester Vane Dimensions (height x dia.) 32x16; 40x20, 50.8x25.4 mm Measuring Range 0 to 240 kPa (0-24 N/cm') Torque Value 5 N - m Extension Rod 500 mm depth. Overall Dimensions (assembled) 310x105 mm Weight 1.3 kg The PRS-ZE0084 Heavy Duty Pocket Penetrometer is designed for making field classification of cohesive soils in terms of consistency, shear strength and approximate unconfined compressive strength. Heavy duty model is all stainless steel construction, three interchangeable tips: 4.5 mm dia. for very hard soil, 6.35 mm for medium and soft soil, 8.98 mm for soft soil. Supplied complete with plastic case. PRS-ZE0084 Heavy Duty Pocket Penetrometer Measuring Range 0 to 10 kgf/cm' Dimensions (assembled) 210 mm length x 20 mm dia. Weight (approx.) 0.5 kg
The clenbuterol rapid test can be used to determine the clenbuterol residue in the tissue.The sensitivity is up to 1ppb. The major advantages of the one step test strip are that results can be obtained within 10 min and that all reagents are included in the test device.It relatively has many other advantages such as lower cost , fewer lable and berif sample preparation than the traditional test methords .
Nkbiotech one step organophosphorus pesticides test strip is a rapid test to qualitatively detect the presence of organophosphorus pesticides in specimens. The major advantages of the one step test strip are that results can be obtained within 10 min and that all reagents are included in the test device.It also relatively has many other advantages such as lower cost , fewer lable and berif sample preparation than the traditional test methods .This product can be used in testing the exist of pesticides in vegetables and fruit rapidly and conveniently outside in the opendoors ., it also possible to detect sulfamethazine below the maximum residue limit in muscle, tissue after a simple sample preparation.
The one step sulfamethazine test strip is a rapid test to qualitatively detect the presence of sulfamethazine in specimens at the sensitivity of 10ppb. The major advantages of the one step test strip are that results can be obtained within 10 min and that all reagents are included in the test strip. It relatively has many advantages such as lower cost , fewer lable and berif sample preparation than the traditional test methods . Using the one step sulfamethazine test strip, it is possible to detect sulfamethazine below the maximum residue limit in muscle, tissue after a simple sample preparation.
It is used for testing mechanical properties of the inspection chambers and the manholes. It can take load test for the chamber body and ring-stiffness test, lateral compression test, Ring-tiffness test for the chamber riser. Beside the above tests, This machine can be also used for various products' external load resistance test. It is ideal testing equipment for factories, mines, science research department. Available standards: Bs en13598-1:2003 plastics piping systems for non-pressure underground drainage and sewerage - unplasticized poly(vinyl chloride) (pvc-u). Polypropylene (pp) and polyethylene (pe) - part 1: specifications for ancillary fittings including shallow inspection chambers Bs en13598-2:2003 plastics piping systems for non-pressure underground drainage and sewerage - unplasticized poly(vinyl chloride) (pvc-u). Polypropylene (pp) and polyethylene (pe) - part 2: specifications for manholes and inspection chambers in traffic areas and deep under Main technical parameters: Max load: 100kn Measuring range: 1%--100% Load resolution:1n Load measuring accuracy: 1% Speed accuracy:5% Load speed: 5-50mm/min Gate model:4.5mïwidth1.8mïength :2.5mïvalid test space22.214.171.124m
Sandeep Garg & Company equipped with the latest XRF analyzers for accurate reading on any metal. Our XRF alloy analyzers are portable hand-held devices that follows stringent quality control norms to ensure the requisite quality of metal scraps as per the contractual standards.
For in vitro qualitative detect of Covid-19 antigen in nasal(NS) swab specimens directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 5 days of the onset of the symptoms. This test is only provided for use by clinical laboratories or to healthcare workers for point-of-care testing, and not for at home testing. 1.Easy to collect samples simple operation without professional equipment. 2.The test results are available in 15 minutes, and the test results are clearly visible. 3.Convenient transportation and low price, higher accuracy. 4.Suitable for large-scale rapid screening. Shelf life: 24 Months Test Result time: 10 Mins Packing: 25 Pieces per Box
Place of Origin: China Brand Name: OEM Model Number: FFN-502 Power Source: manual Warranty: 2 years After-sale Service: Onsite Training Material: Plastic Shelf Life: 2 years Quality Certification: iso Instrument classification: Class III Safety standard: None Type: early wholesale pregnancy test midstream Intend use: female laboratory diagnosis pregnancy test kit Certificate: CE/ ISO9001/ ISO13485 specimen: secretion read time: 10-15mins expiration: 24 months format: cassette,strip method: colloidal gold shipment: by sea/air is available Specification: private label popular pregnancy test
The rapid response antigen Test has been developed in Canada and is approved for utilization in Canada, Peru,Portugal, Brazil, Australia, Kuwait, Indonesia, the Philippines, and many other countries. 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 nasopharyngeal secretions from individuals suspected of COVID-19 within 6 days of symptom onset. This test is also authorized for use with NASAL specimen making it easier for application at POC. The test is authorized for use at the Point of Care i.e., in a patient care setting. Results are for the identification of SARS-CoV-2 viral nucleoprotein antigen. The antigen is generally detectable in nasopharyngeal and nasal secretions during the acute phase of infection
GraceTree COVID-19 IgM/IgG Rapid differential detection kit for IgM and IgG against COVID-19 in human serum, plasma and whole blood Feature & Type : IgM/IgG 1) COVID-19 IgM/IgG : blood test 2) Dual-band results for simple interpretation 3) Multivariable analysis of immunoglobin IgG & IgM 4) Positive percent agreement (PPA) = 96.0% Negative percent agreement (NPA) = 98.99% 5) Room temperature storage ( 2~30C / 36~86F ) 6) Time to result : 2 min 7) Expiration date of this kit is 6 months after its manufacture date 8) MATERIALS PROVIDED - Test device individually foil-pouched with a desiccant - Assay solution in dropping bottle - Capillary tube for sample loading - Instructions for Use - Packing: 1 box of 25 Test units - Product Origin : South Korea - Certificate : FDA EUA Certificate will be proved near 15. September. 2020 - Shipping Terms : FOB - Payment Terms : T/T - MOQ : Under Discussion - Contract : Direct contract seller / Depending on volume, direct contract with a subsidiary of seller which is listed on stock market(in S.Korea) - LOI, POF needed for seller
Top 5 manufacturer in China Produce 100K sets / day Full certificate (FDA, TUV, ANVISA)for sell more than 30 countries. every box contains: 20 Individually sealed foil pouch packed test devices 2 Dilution Buffer vials (12mL/vial) 20 Extraction Tubes 20 packs of swab (2 swabs/pack) 1 Workstation 1 Package insert 1 Positive control swab (on request only) 2 Dilution Buffer vials (12mL/vial) 20 Extraction Tubes 20 packs of swab (2 swabs/pack) 1 Workstation 1 Package insert
USA Manufactured, highly accurate, rapid COVID-19 Antigen test. Clinically validated by third-party medical institutions in USA and Europe (Denmark, Poland). The test is highly specific and sensitive (Specificity 100%, Sensitivity 99.1%). Manufacturer has a decade of experience in rapid testing. Available in either bulk or home-use packaging. Manufcatured and ships out of Miami, Florida.
USA Manufactured, highly accurate, rapid COVID-19 Antibody test. Clinically validated in the USA by Harvard and UCSF Universities, and found to be best-in-class of Antibody tests. 95-100% accuracy in identifying patients after days 12. Manufacturer has a decade of experience in rapid testing. Available in either bulk or home-use packaging. Manufcatured and ships out of Miami, Florida.
SARS-CoV-2 Antigen Test Card Sterilized Swab Extraction Tube Sample Extraction Buffer Instructions for Use Tube Stand (for package with 20 kits) CE license and ISO 13485 certified Our products have been exported to more than 70 countries: Britain, Germany, Italy, Brazil, Argentina, Australia, India, Malaysia, South Africa, etc.
Covid-19 AG (Antigen) Rapid Test Kit *Made in Korea -> Best Quality, No defects, Transparent Business *Our Covid rapid test is rapid and reliable, early identifying an active infection in 15minutes! *High Clinical Sensitivity over 90%! *Clinical Specificity showed 100% for negative patients! *Test procedure: Only 3 steps! (Abbott test kits: 5~8steps) - Method: Immunochromatographic Assay - Test Type: Cassette - Sample Type: Nasopharyngeal Swab - Testing time: Less than 15min - Shelf-life: 18month - Kit Components: Test Device, Test Extraction, Buffer, Filter Cap, Sterilized Swabs for Specimen Collection - Certification: FDA, CE, ANVISA - Certified country: USA, EU, France, Italy, Brazil, Peru, Russia, India, Kazakhstan, Kenya Features: - Result within 15min without instrument required. - 1 step Test without special skill. - High correlation with RT-PCR. - Superior accuracy compared to conventional products. - Room temperature storage for 18months - Cost effective, high performing test desgined for decentralized testing. - Simplify of test method. - Enable intuitive sample processing with prefilled, utilized tubes. *Payment Term: 100% T/T with PO (negotiable)
COVID finger prick, rapid antigen test, or rapid test, is a rapid diagnostic test suitable for point-of-care testing that directly detects the presence or absence of an antigen. It is commonly used for the detection of SARS-CoV-2, the virus that causes COVID-19. Rapid tests are a type of lateral flow tests that detect protein, distinguishing it from other medical tests that detect antibodies or nucleic acid, of either laboratory or point-of-care types. Rapid tests generally give a result in 1 to 15 minutes, require minimal training or infrastructure, and have significant cost advantages. NO Lab Required for results.
Product Description Product Features Product name Realy Tech Novel Antigen Rapid Test Device Saliva Test Certificate CE/ ISO9001/ ISO13485 Specimen Plsama/Serum size - strip(2.5mm,3.0mm, 3.5mm, 4.0mm) cassette(3mm, 4mm) or according to the customers' requirements Sensitivity - over 99.5% Packing Details - strip Cassette 1pcs/foil bag, 50bags/mid-box, 40mid-boxes/carton; in bulk, 2000pcs/carton Shelf Life 2years HIV test cassette Specimen:serum/plasma Model No:HIV-P02D Over 98% accurate conveniency:self-testing The HIV 1/2 Rapid Test Device (Serum/Plasma) detects antibodies to HIV-1 and HIV-2 through visual interpretation of color development on the internal strip. Recombinant HIV-1 and HIV-2 antigens are immobilized on the test region of the membrane. During testing, the specimen reacts with HIV antigen conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there are sufficient HIV-1 or HIV-2 antibodies in the specimen, a colored band will for m at the corresponding test region of the membrane. The presence of this colored band indicates a positive result, while its absence indicates a negative result. The appearance of a colored band at the control region serves as a procedural control,indicating that the proper volume of specimen has been added and membrane wicking has occurred.