Rolling Door Shutter Door Steel Strips C67
Supplier: Taian Henson Metal Co., Ltd., China
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Agriculture Fertilizers & Pesticides · 20 types
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Rolling Door Shutter Door Steel Strips C67
The Rolling Door Shutter Door Steel Strips C67 from EximNext is designed to provide robust security and functionality for commercial and industrial applications. Manufactured using high-quality C67 steel, these strips are engineered to withstand harsh conditions while ensuring longevity and reliability.
Key specifications include:
1. Made from C67 steel grade, known for its high tensile strength and durability, ideal for heavy-duty use.
2. Precision-engineered to fit various rolling shutter systems, ensuring compatibility and ease of installation.
3. Available in multiple dimensions to meet specific project requirements.
4. Offered in bulk supply, catering to large-scale operations and manufacturers.
These steel strips are widely used in warehouses, retail shops, and factories where security is paramount. They provide an effective barrier against unauthorized access while allowing for easy operation and maintenance.
At EximNext, we offer flexible MOQ options to accommodate your business needs. Our rolling door shutter strips come with necessary certifications, ensuring compliance with industry standards for safety and quality. We provide competitive pricing and reliable shipping terms, including FOB and CIF, to facilitate your procurement process.
Choosing EximNext means partnering with verified suppliers and gaining access to a global marketplace, enabling you to source high-quality rolling door shutter door steel strips with confidence.
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Samsung 25 CU FT 3 Door French Door Refrigerator
Introducing the Samsung 25 CU FT Mega Capacity Counter Depth 3-Door French Door Refrigerator, a perfect blend of style and functionality for modern kitchens. This refrigerator not only enhances your kitchen's aesthetics but also optimizes your food storage with its impressive capacity. Its Family Hub feature allows you to connect with family members, manage groceries, and even stream music, making it a truly smart addition to your home.
Key specifications include a spacious 25 cubic feet interior, adjustable shelves for customized storage, and an energy-efficient LED lighting system that illuminates every corner. The advanced cooling technology ensures that your food stays fresher for longer, while the external ice and water dispenser provides convenience at your fingertips. Plus, the sleek counter-depth design creates a built-in look without sacrificing space.
Ideal for residential kitchens, catering businesses, and food service industries, this refrigerator is perfect for bulk supply needs. With competitive pricing and certified quality, it suits a wide array of applications.
EximNext offers flexible MOQ options and competitive trade terms, including FOB and CIF shipping arrangements. We ensure that all our products meet rigorous ISO and CE certifications, guaranteeing you receive export quality goods.
Why choose EximNext? Our verified suppliers bring you the best in wholesale pricing and a global reach, ensuring that your kitchen remains stocked with the finest appliances. Elevate your kitchen experience with the Samsung 25 CU FT Refrigerator today!
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Samsung Bespoke 4 Door French Door Refrigerator
The Samsung Bespoke 4 Door French Door Refrigerator is an innovative appliance that seamlessly blends advanced technology with stylish design. Offered by EximNext, this refrigerator is not only functional but also customizable, allowing you to choose finishes and configurations that fit your kitchen aesthetic. With ample storage space and intelligent features, this refrigerator meets the varied needs of modern households.
Key specifications include a spacious interior with adjustable shelving, energy-efficient operation, and a state-of-the-art cooling system that maintains optimal temperatures for all your food items. The flexible storage options ensure easy organization of groceries, while the innovative SmartThings technology allows you to control and monitor your refrigerator from your smartphone.
Ideal for use in residential kitchens, this refrigerator is perfect for families, food enthusiasts, and anyone looking to enhance their culinary experience.
EximNext offers significant trade benefits, including flexible MOQ and various shipping terms like L/C and T/T. Our verified suppliers guarantee export-quality products with certifications such as CE and ISO. By choosing EximNext, you tap into a global marketplace that ensures competitive pricing and comprehensive support for your bulk supply needs.
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Rapid Antigen Test kit
SARS-CoV-2 Rapid Antigen Test kit Colloidal Gold Method Medical Simple Rapid Convenient Sensitivity : 98.4% Specificity : 98.1% Test Time : 10-15min
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One Step Fecal Occult Blood Rapid Test Cassette
One Step Fecal Occult Blood (FOB) Rapid Test Cassette (Feces) Cat. No.: RH0301T INTENDED USE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is a qualitative detection of human occult blood in feces forself-testing. PRINCIPLE The One-Step Fecal Occult Blood (FOB) Diagnostic Kit is an immunochromatographic sandwich method, which employ two specific monoclonal antibodies to selectively identify hemoglobin in test samples. The result is very specific, and easier to interpret than those of guaiac-based test. The sensitivity is very high with the ability to detect 200ng/ml hemoglobin in feces. In addition, the accuracy of the test is not affected by interfering substances, and dietary restriction is not necessary. STORAGE The kits should be stored at temperature 4-30�°C, the sealed pouch for the duration of the shelf life (24 months). Do the test in 1 hour after open the pouch. WARNING AND PRECAUTIONS 1. For in vitro diagnostic use only. 2. Do not use kit beyond the expiration date. 3. Patient specimens may contain infectious agents and should be handled as though capable of transmitting disease. Wear disposable gloves throughout the specimen collection and assay procedures. 4. The test device should not be reused. REAGENTS AND MATERIALS PROVIDED 1. One pouched cassette with desiccant. 2. One operating Instruction MATERIALS REQUIRED BUT NOT PROVIDED 1. Clock or Timer SPECIMEN COLLECTION AND PREPARATION 1. Collect stool sample by using the sample collection device provided. 2. Unscrew the top of the sample collection device, take out the sample collection stick, and collect the sample by dipping the stick into 3 different places of the stool sample. 3. Put the sample collection stick back in the sample collection device and screw together tightly. 4. If the sample cannot be tested on the day of collection, store the stool sample at 4C. Bring the specimen to room temperature before testing. ASSAY PROCEDURE 1. Remove the test device from foil pouch by tearing along the notch. 2. Specimen collection. Please see also SAMPLE COLLECTION AND PREPARATION 3. Shake the sample collection device several times. 4. Holding the sample collection device upright, carefully unscrew the tip of collection device. 5. Squeeze 2-3 drops of the sample solution on the test sample pad. 6. Read the test results in 5 minutes. INTERPRETATION OF RESULTS Negative: Only one colored band appears on the control region (C). No colored band in the test region (T). Positive: In addition to the control band (C), a distinct colored band also appears in the test region (T). Invalid: If no bands appear, or a test band appears without a control band, the test should be repeated using a new test device.
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One-Step Beta-Lactam Rapid Test
General Information One-Step Beta-Lactam Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Beta-Lactam residue in milk. Specimen: Milk Reading Time : 5-10min
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Malaria Pf/Pv Combo Antigen Rapid Test
INTENDED USE The Malaria Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Plasmodium falciparum (Pf) antigen and P. vivax, P. ovale, or P. Malariea antigen in whole blood. This device is intended to be used as a screening test and as an aid in the diagnosis of infection with Plasmodium. Any reactive specimen with the Malaria Rapid Test must be confirmed with alternative testing method(s) and clinical findings. SUMMARY AND EXPLANATION OF THE TEST Malaria is a mosquito-borne, hemolytic, febrile illness that infects over 200 million people and kills more than 1 million people per year. It is caused by four species of Plasmodium: P. falciparum, P. vivax, P.ovale, and P. malariae. These plasmodia all infect and destroy human erythrocytes, producing chills, fever, anemia, and splenomegaly. P. falciparum causes more sever disease than the other plasmodial species and accounts for most malaria deaths. P. falciparum and P. vivax are the most common pathogens, however, there is considerable geographic variation in species distribution1. Traditionally, malaria is diagnosed by the demonstration of the organisms on Giemsa stained smears of peripheral blood, and the different species of plasmodium are distinguished by their appearance in infected erythrocytes1. The technique is capable of accurate and reliable diagnosis, but only when performed by skilled microscopists using defined protocols2, which presents major obstacles for the remote and poor areas of the world. The Malaria Rapid Test is developed for solving these above obstacles. It detects the antibodies generated in serum or plasma in response to the infection of plasmodium. Utilizing the Pf. specific antigen (HRP-II) and pan-malaria antigen (aldolase), the test enables simultaneous detection and differentiation of the infection of P.falciparum and or P. vivax, ovale, and malariae3-5, by untrained or minimally skilled personnel, without laboratory equipment.
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One-Step Influenza A/B Rapid Test
General information One-step influenza a/b test is detection influenza type a and type b nucleoprotein antigen extracted from the nasal swab specimen. Sensitivity : 91.3% , specificity : 95.7% Detection limit:5.1x105tcid50/ml Specimen: nasal swab Reading time : 15-20min
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HSV IgG/IgM Rapid Test
The Herpes Simplex Virus Rapid Test is a rapid qualitative lateral flow test designed for the quantitive detection of IgG antibodies to Herpes Simplex Virus (HSV) in human serum/plasma samples. HSV-1 is usually associated with infection in oropharyngeal area and eyes, while HSV-2 causes mostly genital and neonatal infections (5, 6), however, the tissue specificity is not absolute (7). HSV-2 can be isolated occasionally from the oropharynx and 5-10% of primary genital infections may be caused by HSV-1. Infants infected with HSV appear normal at birth, but almost invariably develop symptoms during the newborn period (5, 8, 9). Neonatal HSV infection may remain localized or become disseminated. Localized infection may involve one or a combination of sites. These are skin, eyes, mouth or the central nervous system. Disseminated infection is manifested by pneumonitis, hepatitis, disseminated intravascular coagulopathy and encephalitis. Of the infants with neonatal HSV, about one half of those surviving will develop severe neurological or ocular sequelae. A number of serological procedures have been developed to detect antibodies to HSV. These include complement fixation, indirect immunofluorescent antibody, plaque neutralization, and ELISA (6, 8, 10). Antibody of the IgG class is produced during the first 2-3 weeks of infection with HSV and exists only transiently in most patients. Serologic procedures, which measure the presence of IgG antibodies, help discriminate between primary and recurrent infections, since IgG antibodies is rarely found in recurrent infections. High affinity IgG antibodies to HSV, if present in a sample, may interfere with the detection of IgG specific antibody (9). High affinity IgG antibody may preferentially bind to HSV-1 antigen leading to false negative IgG results. Also, rheumatoid factor, if present, along with antigen specific IgG, may bind to IgG causing false positive IgG results. Both problems can be eliminated by deactivating IgG in the sample before testing for IgG.
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TROP I Rapid Test
One Step Troponin Test (Whole blood/Serum/Plasma FOR IN VITRO DIAGNOSTIC USE ONLY SPECIMEN COLLECTION 1. Testing should be performed immediately after the specimens have been collected. Do not leave the specimens at room temperature for prolonged periods. Specimens may be stored at 2-8C for up to 3 days. For long-term storage, specimens should be kept below -20C. 2. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly. MATERIALS PROVIDED 1. Test cards individually foil pouched with a desiccant 2. Plastic dropper 3. Package insert MATERIALS REQUIRED BUT NOT PROVIDED 1. Timer/clock 2. Pipette 3. Controls ASSAY PROCEDURE 1. Read package insert carefully before testing. Allow the test devices, whole blood, serum or plasma to equilibrate to room temperature (15-30C) prior to testing. Do not open pouches until ready to perform the assay. 2. Remove the test device from the foil pouch and use it as soon as possible. 3. Place the test device on a clean and level surface. Hold the dropper provided vertically and transfer 3 drops of specimen (100�µl) to the specimen well (S) in the test device. 4. Wait for the red line(s) to appear. The result should be read between 10 to 15 minutes. INTERPRETATION OF RESULTS 1. Positive Two colored lines should be observed in the viewing window. The line in the test region (T) is the probe line; the line in the control region (C) is the control line, which is used to indicate proper performance of the device. The color intensity of the test line may be weaker or stronger than that of the control line. 2. Negative The control line appears in the test window, but the test line is not visible. 3. Invalid No line appears in the control region. Under no circumstances should a positive sample be identified until the control line forms in the viewing area. If the control line does not form, the test result is inconclusive and the assay should be repeated.
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Rubella Virus Ab IgG/IgM Rapid Test
1. The One Step RV IgG/IgM Test can be performed used on Whole Blood /Serum / Plasma. 2. To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures. 3. Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. For long term storage, specimens should be kept below -20â??. Whole blood should be stored at 2-8â?? if the test is to be run within 2 days of collection. Do not freeze whole blood specimens. 4. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly. Test Procedure Allow the test, specimen, buffer and/or controls to reach room temperature 15-30â?? (59-86â??) prior to testing. 1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible. 2. Place the test device on a clean and level surface. 3. Hold the dropper vertically and transfer 1 drop of specimen (approximately 10μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below. 4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes. Interpretation of Results Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of RV specific IgG antibodies. The appearance of T1 test line indicates the presence of RV specific IgM antibodies. And if both T1 and T2 line appear, it indicates that the presence of both RV specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is. Negative: One colored line appears in the control region(C). No apparent colored line appear in the test line region. Invalid: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.
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Toxoplasma Gondii IgG/IgM Tri-Lines Rapid Test
Uncut Sheet Toxoplasma Gondii IgG/IgM Tri-Lines Rapid Test Specimen :Whold Blood/Serum/Plasma INTENDED USE The One Step TOXO IgG/IgM Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Toxoplasma gondii in Whole Blood /Serum / Plasma to aid in the diagnosis of TOXO infection. Toxoplasma gondii is an obligate intracellular protozoan parasite with a worldwide distribution. Serological data indicates that approximately 30% of the population of most industrialized nations is chronically infected with the organism. A variety of serologic tests for antibodies to Toxoplasma gondii have been used as an aid in diagnosis of acute infection and to assess previous exposure to the organism. These tests are the Sabin-Feldman dye test, direct agglutination, indirect hemagglutination, latex agglutination, indirect immunofluorescence, and ELISA. Recently, lateral flow chromatographic immunoassay, such as The Toxo IgM/IgG Rapid Test (Whole Blood/Serum/Plasma) was introduced into the clinic for the serodiagnosis of Toxoplasma gondii infection. One step TOXO IgG/IgM Test is a simple, visual qualitative test that detects TOXO antibodies in human Whole Blood/serum/plasma. The test is based on immunochromatography and can give a result within 15 minutes. Storage and Stability Store as packaged in the sealed pouch at room temperature or refrigerated (4-30â?? or 40-86â??). The test device is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use.
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HCG Serum/Urine Rapid Test
INTENDED USE The HCG s/u Gold Rapid Screen Test(RST)is a chromatographic immunoassay for the early detection of human chronic gonadotropin (HCG) in serum/plasma or urine specimens. INTRODUCTION HCG is a glycoprotein hormone secreted by the developing placenta during pregnancy. The concentration of HCG in serum is approximately equal to the concentration in urine. The concentrations of HCG in urine and serum continue to rise during the first trimester of pregnancy to as high as 100,000 mIU/ml. HCG appears in urine shortly after conception, and continues to increase during the early stages of pregnancy, making it an excellent indicator for the detection of pregnancy. PRINCIPLE The membrane of the test device was coated with anti HCG antibodies on the test region and goat anti mouse IgG antibodies on the control region. During the test, urine specimen is allowed to react with the HCG monoclonal antibody-colloid gold conjugate, which was pre-dried on the test strip. The mixture then moves upward on the membrane chromatographically by capillary action. For a positive specimen, the conjugate binds to the HCG forming an antibody-antigen complex. This complex is captured by anti HCG antibody immobilized on the test region (T) and produces a pink color band when HCG concentration is equal to or greater than 25mIU/ml. Absence of this colored band in the test region suggests a negative result. To serve as a procedural control, a colored band at the control region(C) will always appear regardless the presence or absence of HCG. STORAGE
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Nitrofurans Rapid Test(AOZ,AMOZ, AHD, SEM)
General Information One-Step Nitrofurans Rapid Test are competitive immunoassay for the semi-quantitative detection of the presence of AOZ,AMOZ, AHD, SEM residue in animal tissue. Detection limit:AOZ 1ppb , AMOZ 1ppb , AHD 1ppb , SEM 1ppb Specimen: Animal tissue Reading Time :10-15 min
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One-Step Bovine Brucella Ab Rapid Test
General Information Method: Double Antigens Sandwich Method Sensitivity : 99.5% Specificity : 98.8% Specimen : Serum / Plasma Reading Time : 5- 10 min
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One-Step Tetracycline Rapid Test
General Information One-Step Tetracycline Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Tetracycline residue in Milk,Honey,Tissue extract and Aquatic products. Detection limit: Milk 100 ppb ,Honey 20ppb , Tissue extract 100 ppb , Aquatic products 100ppb Specimen: Defatted milk, Honey, Tissue extract, Aquatic products Reading Time : 5-10min
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Quinolone Rapid Test(Milk)
Antibiotics Residue In Milk Rapid Test(Quinolone Rapid Test) INTENDED USE Quinolone Test is a competitive immunoassay for the semi-quantitative detection of the presence of Quinolone in milk. Cut-off: 50 ppb Assay Time: 10 - 15 min Sample: milk PRINCIPLE OF THE ASSAY Quinolone Test is based on competitive lateral flow immunochromatographic assay. The Quinolone conjugate in the test zone will capture the immuno-gold, when there is very little dissociative Quinolone in the sample. A visible red test band indicates a negative result when the control line shows that the card is valid. The test band will be not visible if Quinolone is present in concentration of 50 ppb and above which explains a positive result.
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Covid-19 IgG/IgM Rapid Test Cassette
Name Testing kit for New coronavirus (2019-nCOV) IgG/IgM antibody Rapid Test WB/S/P Specifications 25 tests Introduce This kit uses the colloidal gold immunochromatographic principle to qualitatively detect novel coronavirus igg/igm antibodies in human serum, plasma, or whole blood. the sample to be tested was added to the sample hole of the test paper, and then added 2 drops of sample diluent. the igg/igm antibody in the sample combined with the recombinant new coronavirus antigen labeled with the colloidal gold on the binding pad formed complex. under the action of chromatography, it diffused forward along the nitrocellulose membrane (nc membrane). the nitrocellulose membrane was fixed with two detection lines (g line, m line) and one quality control line (c line). the g line was fixed with anti-human igg antibody for the detection of new coronavirus igg antibody; the m line was fixed with anti-human igm antibody for the detection of new coronavirus igm antibody; and the c line had quality control for the detection of the new coronavirus ig antibody. If the sample contains a new coronavirus IgG antibody, then the antibody binds to the recombinant new coronavirus antigen labeled with colloidal gold, diffuses forward, and then binds to the anti-human IgG antibody fixed on the NC membrane detection line (G line). if the sample contains a novel coronavirus igm antibody, then the antibody binds to the recombinant new coronavirus antigen labeled with colloidal gold, diffuses forward, and then binds to the anti-human igm antibody fixed on the nc membrane detection line (m line). The darker the color of the colloidal gold accumulated on the detection line, the higher the concentration of the new coronavirus antibody in the sample. To monitor the effectiveness of the test card, set up a quality control line (line C), whether there is a detection line (line T), quality control line (line C) should be color, otherwise the test results are judged invalid. Storage Stored at 4 to 30c and valid for 18 months. After the aluminum foil bag is unsealed, please use it as soon as possible. Sample 1. It is suitable for human serum, plasma and whole blood samples. 2. The samples should be used as soon as possible; if they cannot be used immediately, the serum / plasma samples should be kept at 2-8C for 5 days and -20C for long-term preservation; the whole blood samples should be placed at 2-8C to avoid hemolysis; 3.The sample contains a large amount of lipids, hemolysis or turbidity, do not use, so as not to affect the judgment of the results.
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Giardia Ag Feces Rapid Test
The Giardia Ag Feces Rapid Test from EximNext is a cutting-edge diagnostic tool designed for the qualitative detection of Giardia lamblia antigens in fecal samples. This rapid test employs a sandwich lateral flow immunochromatographic assay, providing quick and reliable results in a matter of minutes. With its user-friendly design, this test facilitates easy and efficient screening for giardiasis, a common intestinal infection.
Key features include its high sensitivity and specificity, ensuring accurate detection of Giardia antigens, which is crucial for effective diagnosis and treatment. The test is designed for use in various clinical settings, including hospitals, clinics, and laboratories, making it an essential tool for healthcare professionals. Additionally, it requires minimal training for use, further enhancing its practicality.
This product is particularly valuable in the healthcare and diagnostic industries, where rapid and accurate testing is critical for patient care. It is also suitable for use in veterinary practices, allowing for efficient testing of animals suspected of giardiasis.
EximNext offers flexibility in minimum order quantities (MOQ) and ensures that our Giardia Ag Feces Rapid Test complies with international certifications, providing peace of mind regarding its quality. Various packaging options are available, and we guarantee prompt shipping under FOB and CIF terms, with payment options including L/C and T/T.
When you choose EximNext, you are assured of sourcing from verified suppliers, enjoying competitive pricing, and leveraging our global reach to obtain this essential diagnostic tool.
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Dengue Ns1 Rapid Test
The Dengue NS1 Rapid Test by EximNext is a cutting-edge diagnostic tool designed for the swift and reliable detection of Dengue virus infections. This test provides healthcare professionals with immediate results, essential for timely diagnosis and patient management in endemic areas. With its user-friendly design and accurate results, this rapid test is a must-have for clinics, hospitals, and health centers.
Key specifications include high sensitivity and specificity rates, ensuring accurate detection of the NS1 antigen during the early phase of infection. The test is easy to administer and requires minimal training, making it accessible for various healthcare settings. Results are available in just 15 minutes, significantly speeding up the diagnosis process.
The Dengue NS1 Rapid Test is critical in regions where Dengue fever is prevalent, assisting in effective patient management and outbreak control.
EximNext offers flexible MOQ options, allowing healthcare providers to stock according to demand. Our rapid tests are certified by ISO and CE, ensuring compliance with international standards. Each test kit is meticulously packaged to maintain product integrity and is shipped under reliable terms including L/C and T/T.
By choosing EximNext, you leverage our global reach and partnerships with verified suppliers, ensuring competitive pricing and consistent supply of essential diagnostic tools.
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About flexible rapid door Trade
flexible rapid door is one of the most actively traded commodities in global B2B markets. Major exporting countries include Ukraine, Russia, Argentina, and India, which together account for over 80% of global production. Buyers from the Middle East, Africa, and Southeast Asia represent the largest import demand.
When sourcing flexible rapid door, buyers typically evaluate suppliers based on price per metric ton, minimum order quantities, certifications (ISO, HALAL, SGS), and payment terms. The most common payment methods used in flexible rapid door trade are Letter of Credit (L/C) and Telegraphic Transfer (T/T).
EximNext connects buyers with 1,240+ verified flexible rapid door suppliers across 67 countries. Post a buy requirement to receive competing quotes within 24 hours, or browse our verified supplier directory to compare prices, certifications, and response times.
Search Products on EximNext — Source From Verified Global Suppliers
This is the EximNext product search page — one place to search across our entire B2B catalogue of wholesale and export-ready products. Type any product name, material, grade, or HS-style keyword into the search bar above and instantly browse matching listings from verified manufacturers, suppliers, exporters, and wholesalers in more than 200 countries. Whether you are sourcing raw materials, components, machinery, or finished goods, the search brings the right products and the right factories to one screen so you can compare and shortlist in minutes instead of days.
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