Bids Are Invited For Price Registration For The Acquisition Of Various Kits For Immunocromat Tests (Rapid Tests) For Various Diseases

Hidden Blood Test In The Stool. One Step Type Or Similar. No Diet. Rapid Test By Immunocromatographic Methodology Or Similar Recognized In The Laboratory Environment., Test For Qualitative And Quantitative Determination Of Vdrl By Flocculation, Using Cardiolipin Antigen. Application: To Detect Nonspecific Antitreponemic Antibodies. Contains Positive Control., Waaler Rose Test By Hemaglutination. Contains Positive Control., Le Cell Test By Latex Agglutination Or Similar Methodology, Provided It Is Rapidly Accomplished. Contains Positive Control., Qualitative Testing By The Immunocromatographic Method For Determining Hcg In Serum And Urine. With Sensitivity Of 25 Iu. Presentation: Individual Packaging., 16/04/2025, Testing Of Rotavirus Determination In Feces By The Latex Agglutination Method Or Immunocromatographic On Tape Or Cassette, Or Similar Technology. With Quality Control., Quick In Vitro Immunocromatographic Test For Qualitative Detection Of Symptomic Swab Antigen Antigen (Vrs) Antigen (Vrs) Samples, Nasal And Aspirated Washing Of Symptomatic Patients., For Qualitative Dehydrogenase Glutamate Detection (Gdh) And Toxins A And B Of Clostridium Difficile In Stool Samples., Duo Duo Immunocromat Test (Combo) Fast, For Qualitative Detection Of Antibodies Igg/Igm And Antigen Ns1 Of The Parallel Dengue Dengue Virus. The Test Should Allow The Use Of Total Blood, Serum And Plasma., For Qualitative Detection Of Igg/Igm Antibodies Of The Zika Virus. The Test Should Allow The Use Of Total Blood For Qualitative Detection Of Igg/Igm Antibodies From Chikungunya Virus. The Test Should Allow The Use Of Total Blood, Fast In Vitro Immunochromatographic Test For Qualitative Detection Of Covid-19 Virus Antigen In Human Nasopharyngeal Secretion Samples. Presentation: In Appropriate And Reinforced Packaging That Ensures The Integrity Of The Product. Label Containing: Batch Number, Date Of Manufacture, Validity And Origin. Minimum Validity: 12 (Twelve) Months After Delivery., For The Detection And Qualitative Differentiation Of Antigen Of The Influenza Causing Human Samples Of Nasopharyngeal Secretion, With Differentiation For Type B Influenza Viruses, Influenza Type A And H1n1 Mutation, Should Have A Specific Region For Determination. Presentation: In Appropriate And Reinforced Packaging That Ensures The Integrity Of The Product. Label Containing: Batch Number