Supplier: Disposable gloves, balloons, soft sterile 1 ml medical droppers
Plastic dropper pack Manufactured using American jomar injection blow molding process in a clean room environment and conforms to pharma standards. Set comprises of bottle, nozzle and a cap Pack consists of two system 1. With open nozzle and a tamperevident cap in which case end user have just to open the pilferproof cap and dispence the medication 2. Blocked nozzle with a cap to pierce the blocked nozzle just before usage Sizes ranges from 5,10,15ml to 500ml. One carton consists of 2000 sets fo bottle, nozzle and cap. The gross wt of the 2000 sets with the carton is approximately 12kg.
Clarification of a possibly already occurred immune reaction of the body against SARS-CoV-2 by determination of the specific IgM and/or IgG immunoglobulins (Antigens: S1, S2 and N Proteins). Price-Details: 25% discount for government, clinics and medical facilities. Companies will only receive the discount if they can prove that they use the product for their own purposes and not for commercial purposes. Ask for special deal for 1,000,000 units and more. Performance: The rapid test has a very high accuracy because - unlike most rapid blood tests and laboratory tests - it uses 3 proteins (S1, S2 and N) to detect the antibodies (so-called trinity method). The significance of the rapid test increases during the course of the infection with the formation of antibodies in the blood (between day 4-11 in about 70% of patients). The overall sensitivity of the test (IgM/IgG) is 98.6% (> 1,100 clinical trials). The specificity of the test (reaction only to Covid19) is 99.5% (> 1,500 clinical trials). Please compare this with other tests! Advantages Quick result: The rapid test shows a significant result within 20 minutes. Test procedure: We provide a simple and fast test procedure with two drops of blood from the fingertip, from venous blood or from unfrozen serum. Certified Quality: The test is â??Made in Germany with CE conformity declaration and fulfils the FDA & WHO-requirements. What is included per unit: 1x Cassette (Polystyrene) 1x Support Pad (PVC 3.0 x 60 mm) 1x Cellulose Nitrate Membrane (Cellulose nitrate membrane coated with mouse, anti-human IgM and IgG antibodies) 1x Specimen Pad (Glass fiber / GF) 1x Liquid Absorption Pad (Cellulose acetate membrane) 1x Chemical Coupling Pad (Sealed glass fiber, coated with SARS-CoV-2 antigens and mouse IgG controls) 2g Desiccant (Molecular sieve desiccant) 1x, Aluminum Foil Package (12 x6.5 cm, three-layers of aluminum foil paper) 1x Tag (80 x 50 mm, single-sided plastic tag) 1x Sealable Bag (A sealable bag for disposal of the used cassette) 1x Lancet (Lancets for fingerstick whole blood only) 1x Plastic pipette (A transfer plastic pipette with the line mark of 50 ) 1x Squeezable plastic liquid dropper ampoule (Plastic ampoule containing dilution buffer 1) 1x Instructions for Use
Intended use: AIVD COVID-19(SARS-CoV-2) IgG/IgM Rapid Test is a single use, rapid device for qualitative detection of total antibodies against 2019 novel coronavirus (SARS-CoV-2) in human serum, plasma or whole blood specimens. The kit is intended for screening of patients suspected for infection with SARS-CoV-2, and as an aid in the diagnosis of the coronavirus disease 2019 (COVID-19). Descriptionï¼? Novel coronavirus pneumonia (NCP) or SARS-COV-2, that was officially named by the WHO as â??Corona virus disease 2019â?? (COVID-19), is a respiratory infection caused by a new virus that was first identified in late 2019. IgM/IgG Rapid Kit can specifically detect IgM and IgG antibodies of COVID-19, covering the entire course of infection and recovery period of patients. This approach improves the overall diagnosis of COVID-19 in both acute and recovery phases of illness. This kit utilizes the principle of colloidal gold immunochromatography to qualitatively detect the new coronavirus (COVID-19) IgG / IgM antibodies in human serum and plasma. Lateral flow immunochromatographic assay provides an easy workflow, short turnaround time, and rapid diagnosis of COVID-19 suspected patients. This method does not require expensive medical instruments and consumables. Just take the specimen and add it to the sample well, and then add the required amount of a diluent. The IgG / IgM antibodies in the sample will interact with the colloidal gold-labeled COVID-19 recombinant antigen on the conjugate pad. Then the conjugate pad will release re-solubilized conjugate onto the nitrocellulose membrane. The nitrocellulose membrane (NC membrane) diffuses it forward. As the sample moves along the device binding reagents situated on the nitrocellulose membrane bind to the target at the test line. If the sample contains a COVID-19 IgG antibodies, they will bind to the colloidal gold-labeled novel coronavirus recombinant antigen, diffuse forward, and then react with the anti-human IgG antibodies immobilized on the NC membrane detection line (T2 line). Similarly, if the specimen contains IgM antibodies to COVID-19, the antibodies will react with antigen-coated particles, the conjugate migrate laterally forward, and cause a colored line (T1 line). The darker the color of colloidal gold on the test line, the higher the concentration antibodies to COVID-19 in the sample. Accuracy:ï¼?> 90% Specificity: 97% Basic Protocolï¼? 1. Remove the test specimen, required reagents from storage conditions, and equilibrate to room temperature. 2. Unpack the aluminum foil bag, place the test horizontally on the table and number it. 3. Add 10ul serum, plasma or whole blood sample to the sample well with a pipette or a dropper. Slowly add 2 drops of sample dilution (about 60uL) to the sample well. 4. Read the results within 10-15 minutes after adding the sample, and the results will be invalid after 30 minutes.
CTK Biotech's, CE Certified , the OnSite Typhoid IgG/IgM Combo Rapid Test is a lateral flow immunoassay for the detection and differentiation of IgG and IgM anti-Salmonella typhi (S. typhi) and paratyphi in human serum, plasma or whole blood. Product Description Utilizes O Antigen And H Antigen From Both Typhi And Paratyphi Serovars To Maximize Sensitivity Differentiates Between Igg And Igm To Determine Stage Of Infection One Step Procedure Minimizes Operator Error Due To Sample Preparation High Level Of Reproducibility Test Kits Can Be Used And Stored In A Wide Range Of Temperatures Product Specification:- Brand Name : CTK Biotech Pkg Qty : 1 Number Of Items : 30 Specifications : Test Result Within 15 Minutes Allows Medical Professionals To Take Immediate Action Contains1 : Individually Sealed Foil Pouches Containing:One Dip Strip Device,One Desiccant,Plastic Droppers,Sample Diluent (ref Sb-R0160, 5 Ml/Bottle)
The PocRoc SARS-CoV-2 Neutralizing Antibody Rapid Test Kit is developed for in vitro qualitative detection of SARS-CoV-2 neutralizing antibodies in human serum, plasma, or whole blood samples. SARS-CoV-2 Neutralizing antibody is an important marker for assessing the effectiveness of the SARS-CoV-2 vaccines. The reagent is for neutralizing antibody detection in samples from individuals after vaccine injection or recovered from COVID-19. PocRoc�® SARS-CoV-2 Neutralizing Antibody Rapid Test Kit has great significance for the development of SARS-CoV-2 vaccines, evaluation of effectiveness, and evaluation of neutralizing antibody levels in human bodies. For Medical Professional Use Only! TEST PROCEDURE Do not open the sealing strip until you are ready to perform a test, and the single-use test is suggested to be used under a low environment humidity (RHâ?¤70%) within 1 hour. 1. Allow all the components of the kit and specimens to reach room temperature prior to testing. 2. Take out the test card and place it on a clean dry surface. 3. Identify the test card for each specimen. 4. Use a dropper to deliver one drop (~40�¼l) of serum, plasma, or whole blood samples into the sample well on the test card, followed by one drop (~40l) of sample buffer. 5. Start the timer and read the result immediately after 15 minutes, and the result after 30 minutes is invalid.
