Ultrasonic Diagnostic Apparatus Product Description - Abdominal,Obstetrics,Gynecology, Cardiology, Neural and Small parts Price of product ( USD price or FOB price) - 3000/per unit Product origin - China Key Specifications/Special Features - 1.Color 12.1' LED monitor with high resolution, USB port; 2.Light weight of 2.5kgs, and Laptop design; 3.Built-in battery can drive the main unit to work for more than 3 hours; 4. General, OB/GYN, cardiology, urinary, small organs, and so on 5. VGA Outpout,AV Outpout,working station, connect with computer, external monitor and HP printer directly Minimum Order Size and Packaging details - 1pcs
3-part Hematology Reagents & Instruments (branded, Oem For Mindray, Sysmex Etc), Hematology Controls From Diagon, Hungary (long Shelf Life & Long Open Vial Stability) Rapid Card Tests For Malaria, Dengue, Chikungunya Etc Clinical Chemistry Reagents Elisa Kits For All Parameters Elisa Reader & Washer For Any Further Diagnostics Solution, Contact Us.
Medical diagnostic reagents, full range of hepatitis diagnostic kits some of our kits are ce-marked. We have elisa and rapid test kits.
Diagnostic tool Features Universal dash programmer is the most sold programming-device for digital speedometers worldwide. The system is a high-quality tool, which offers a maximum of flexibility and working comfort despite simplest operation. You can serve almost any vehicle with the tacho universal. Specification Outstanding characteristics of our programming system are: 1.The current odometer reading is decoded and shown in the lcd display 2.Easy self explanitory operation by clear menu guidance 3.Backlit display makes working possible in overcast conditions 4.All datasets can be edited, saved and loaded 5.The stored data can be transferred to a pc for archiving 6.Up to 200 files can be stored in the universal dash programmer 7.Broken speedometers can be repaired comfortably 8.You receive further developed software from us by internet 9.New types and manufacturers can be released within seconds by telephone. There is no need to send the unit to us.
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
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
General Information One-Step Quinolone Test is a competitive immunoassay for the semi-quantitative detection of the presence of Quinolone in milk ,honey,tissue extract and aquatic products sample. Detection limit: Milk 50 ppb ,Honey 50ppb , Tissue extract 50ppb , Aquatic products 20ppb , Specimen: Milk ,Honey,Tissue extract,Quatic products Reading Time : 5-10 min
General Information One-Step Sulfonamides Rapid Test is a competitive immunoassay for the semi-quantitative detection of the presence of Sulfonamides residue in Milk,Honey,Tissue extract and Aquatic products. Specimen: Milk, Honey, Tissue extract, Aquatic products Reading Time : 5-10 min
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 animals tissue. Detection limit:AOZ 1ppb , AMOZ 1ppb , AHD 1ppb , SEM 1ppb Specimen: Animals tissue Reading Time :10-15 min
General Information One-Step Ractopamine Rapid Test does not require any equipment for the detection of pig urine,Tissue and Feed Ractopamine residues. Detection limit: 3ppb Specimen: Urine, Tissue ,Feed Reading Time :3-5 min
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 4-30C, 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 1Clock 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.
Intended use The malaria rapid test is a lateral flow chromatographic Immunoassay for the simultaneous detection and differentiation of plasmodium falciparum (pf) 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. Storage Store the test kits at room temperature 4- 30 degrees c. The sealed pouch has a self life of 24 months.Of transmitting disease.
Uncut Sheet Influenza A/B Rapid Test Specimen:nasal swab Intended Use The Influenza A +B Test is a rapid chromatographic immunoassay for the qualitative detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. This kit is intended to be used as an aid in the diagnosis of influenza A and influenza B virus in nasal swab specimens. Principle The Influenza A +B Test is a qualitative membrane strip based immunoassay for the detection of influenza type A and B nucleoprotein antigens in nasopharyngeal swab and nasal aspirate specimens. In this test procedure, influenza type A antibody is immobilized in the A line, influenza type B antibody is immobilized in the B line. After a specimen is placed in the specimen well, it reacts with influenza type A antibody and/or B antibody coated particles that have been applied to the specimen pad. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized antibody. If the specimen contains influenza type A, a colored line will appear in the A line region indicating a influenza type A positive result. If the specimen contains influenza type B, a colored line will appear in the B line region indicating a influenza type B positive result. Absence of any T lines (A and B) suggests a negative result. To serve as a procedural control, a colored line will always appear at the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred. Storage and Stability 1.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. 2.The test must remain in the sealed pouch until use.
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.
Intended Use The Malaria Gold Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of antibodies including IgG, IgM and IgA to Plasmodium falciparum (Pf) and vivax, ovale, and malariea (Pv.o.m) 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 Gold Rapid Test must be confirmed with alternative testing method(s) and clinical findings. Reagents And Materials Provided 1. Each kit contains 25 test devices, each sealed in a foil pouch with three items inside: a. One cassette device. b. One plastic dropper. c. One desiccant. 2. Sample diluent (1 vial, 5 ml) 3. One package insert (instruction for use). Materials Required But Not Provided 1. Clock or Timer 2. Lancing device for whole blood test
Uncut Sheet Hiv 1/2 Tri-lines Rapid Test Package:30sheets/pouch Specimen:Whole blood/Serum/plasma Intended Use The HIV-1/2 Rapid Screen Test (RST) is a qualitative test for the detection of antibodies to Human Immunodeficiency Virus type 1 and 2(HIV-1/2) in human serum/plasma and whole blood. It is considered as an initial screening test for HIV-1/2 antibodies. All positive specimens must be confirmed with Western Blot or other qualified EIA. Precaution 1.For in vitro diagnostic uses only. 2.All patient samples should be treated as if capable of transmitting diseases. 3.Do not use test kit beyond expiration date. 4.Icteric, lipemic, hemolysed, heat treated and contaminated sera may cause erroneous results. Summary And Explanation Of The Test It has been shown that the acquired immunodeficiency syndrome (AIDS) is caused by viruses transmitted by sexual contact, transfusion, use of contaminated blood products and sharing contaminated needles. HIV-1 and HIV-2 viruses have been isolated from patients with AIDS and AIDS-related complex (ARC), high-risk persons for AIDS. HIV-1 and HIV-2 viruses delete T helper cells, a subpopulation of T cells for body defense, thus causing AIDS patients susceptible to opportunistic infections and developing malignant tumors. The incidence of specific antibodies to HIV-1/2 is high in AIDS, ARC and persons with high risk for AIDS. The HIV-1/2 Rapid Screen Test is designed to detect antibodies to HIV-1/2 in AIDS patients, ARC or high risk persons and identify any potential donors carrying these antibodies in serum specimens. Principle HIV-1/2 RST is a chromatographic immunoassay (CIA) for the detection of antibodies to HIV-1/2 in human serum/plasma and whole blood. HIV-1/2 specific antigens are precoated onto membrane as a capture reagent on the test region. During the test, specimen is allowed to react with the colloidal gold particles, which have been labeled with HIV-1/2 specific antigens. Antibodies to HIV-1/2, if present, a red colored band will develop on the membrane in proportion to the amount of HIV-1/2 antibodies present in the specimen. Absence of this red colored band in the test region suggests a negative result. To serve as a procedural control, red colored band in the control region will always appear regardless the presence of antibodies to HIV-1/2.