I Would Like To Talk To You About Our New Covid-19 Antibody Testing Dear Medical Distributor, My name is Alexander Camman,I have recently been in charge of all the business done in Peru. WHPM Established in 1993 in Los Angeles California, has been designated a GMP registered center for in vitro diagnostic medical devices by the FDA. Our IFOB colon cancer test is the #1 sold in the world. I wanted to contact and introduce myself, as I will be your dedicated account manager and main point of contact here at WHPM, to make sure that all your needs are taken care of. I'm excited to tell you about our new COVID-19 quick test that is CE Certified and made in the United States of America.. I would love to discuss how we can help introduce these products into your company's product line. What is the best way to contact you? I am open to communication on various platforms; mainly by phone, Email or Whatsapp. However, if you prefer another method of communication please let me know! Please see all my contact options below. If you are interested you can contact me Direct. Thank You For Your Time
* Manufactured by Guangzhou Wondfu Biotech Co., Ltd, the leading and publicly traded corporation authorized to manufacture and distribute COVID anti-body rapid tests * Diagnosis for COVID-19 with instant result in 15 minutes * Detection for both IgG and IgM antibody
COVID-19 (Sars-CoV-2) antibody test kit now available. -Diagnosis for coronavirus disease (COVID-19) -Easy to use, instant result in 15 minutes Product name : SARS-CoV-2 Antibody Test (Lateral Flow Method) Packing size : 20 tests per box Reaction Time] : 15 mins Sample type : Whole blood, serum and plasma Storage condition : 2~ 30 Shelf life : 12 months Qualification : CFDA, CE
High accuracy High quality, with CE certificate. 10 tests per box
COVID-19 IgM/IgG Antibody Detection Kit (Colloidal Gold Immunochromatography) is suitable for the qualitative detection of COVID-19 by detecting SARS-CoV-2 IgM/IgG antibodies in human serum, plasma, or whole blood. Common signs of infection with SARS-CoV-2 include respiratory symptoms, fever, cough, shortness of breath, and dyspnea. In more severe cases, infection can cause pneumonia, severe acute respiratory syndrome, kidney failure, and even death. SARS-CoV-2 can be excreted through respiratory secretions or transmitted through oral fluids, sneezing, physical contact, and through air droplets
We are a manufacturer of SARSCoV2 RAPID TEST CASSETTE in China. We can provide customers following SARSCoV2 rapid testing products that have obtained the CE or other certifications. And has been exported to Thailand, the Philippines, Germany, Italy, Ecuador, South Africa and other countries. SARSCoV2 IgG/IgM Rapid Test Cassette; SARSCoV2 Antigen Rapid Test (nasopharyngeal swab); SARSCoV2 Antigen Rapid Test (Saliva); SARSCoV2 and Influenza A+B Antigen Combo Rapid Test; SARSCoV2 Neutralizing Antibody Test Kit;
Test type : Antibody (one drop of finger stick blood, 15 minutes detection time) Packing : Individually packed 10 test kits per box Available Certificates : FDA registered, CE, ISO 13485:2016 MOQ : 8000 pcs / 1 Pallet
PANODYNE - The new rapid lgM-lgG combined antibody test* for COVID-19 from Multibrands International is now available to test for the detection of lgG and lgM antibodies of coronavirus from a small specimen of human serum, plasma or whole blood. The detection works with proteins to indicate if a person's immune system has responded with the COVID-19 virus to indicate infection.
Product Description - COVID-19 Test Kit: ANTIBODY Price of product ( USD price or FOB price) - Quantity dependent Product origin - Switzerland Key Specifications/Special Features - CE Mark: 96%/92% sensitivity; 100%/100% specificity (clinical). Approx. 10 minute result time Minimum Order Size and Packaging details - 1000 10 per box, 100 box minimum
The kit is intended for the in vitro qualitative determination of Novel Coronavirus (2019-nCoV) IgG/IgM antibody in human serum, plasma or whole blood. Testing is limited to supplementary detection indicator for suspected nucleic acid negative results or in conjunction with nucleic acid detection in the diagnosis of suspected cases. It should not be used as the basis for diagnosis and exclusion of Novel Coronavirus Pneumonia.
