Occult Blood In Stools, Type One Step Or Similar, Without Diet. Rapid Test Using Immunochromatographic Or Similar Methodology Recognized In The Laboratory Environment, Qualitative And Quantitative Determination Of Vdrl By Flocculation, Using Cardiolipin Antigen, To Detect Nonspecific Antitreponemal Antibodies. Containing Positive Control, Waaler Rose By Hemagglutination, Containing Positive Control, Le Cell By Latex Agglutination Or Similar Methodology, As Long As It Is Quickly Performed. It Must Contain Positive Control, Qualitative Test Using The Immunochromatographic Method For The Determination Of Hcg In Serum And Urine, With A Sensitivity Of 25 Iu, In Individual Packaging, Determination Of Rotavirus In Feces Using The Latex Agglutination Method Or Immunochromatographic Method On A Strip Or Cassette Or Similar Technology, Rapid, Quality Controlled, Rapid In Vitro Immunochromatographic Test, For The Qualitative Detection Of Respiratory Syncytial Virus (Rsv) Antigen In Clinical Samples Of Nasopharyngeal Swabs, Nasal Washes, And Respiratory Tract Aspirates From Symptomatic Patients, For The Qualitative Detection Of Glutamate Dehydrogenase (Gdh) And Clostridium Difficile Toxins A And B In Stool Samples, Rapid In Vitro Duo (Combo) Immunochromatographic Test, For The Qualitative Detection Of Igg/Igm Antibodies And Dengue Virus Ns1 Antigen In A Parallel Run. The Test Should Allow The Use Of Whole Blood, Serum And Plasma, For The Qualitative Detection Of Igg/Igm Antibodies To The Zika Virus. The Test Must Allow The Use Of Whole Blood For The Qualitative Detection Of Igg/Igm Antibodies To The Chikungunya Virus. The Test Should Allow The Use Of Whole Blood, A Rapid In Vitro Immunochromatographic Assay, For The Qualitative Detection Of The Antigen Of The Virus That Causes Covid-19 In Human Samples Of Nasopharyngeal Secretion. Minimum Validity Of 12 Months After Delivery. Presentation In Appropriate And Reinforced Packaging That Guarantees The Integrity Of The Product. Label With Batch Number, Date Of Manufacture, Expiration Date And Origin, For The Detection And Qualitative Differentiation Of The Antigen Of The Virus That Causes Influenza In Human Samples Of Nasopharyngeal Secretion, With Differentiation For The Influenza Virus Type B, Influenza Virus Type A And The Mutation H1n1 (Must Have Specific Region For Determination). Minimum Validity Of 12 Months After Delivery. Presentation In Appropriate Reinforced Packaging That Guarantees The Integrity Of The Product. Label With Batch No.
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