Bids Are Invited For Price Registration For Eventual Future Acquisition Of Rapid Test Kit, Analysis Of Laboratory Tests And Biopsy, For The Municipal Health Secretariat.
Bids Are Invited For Price Registration For Eventual Future Acquisition Of Rapid Test Kit, Analysis Of Laboratory Tests And Biopsy, For The Municipal Health Secretariat.
Quick Test For Ns1 Antigen Detection For Dengue Virus. Quick Test Immunocromatographic Testing Of Lateral Flow For Qualitative Detection Of Dengue Virus Antigen (Den-1, Den, Den3, And Den). The Test Should Allow Reliable Diagnosis With Minimum Specificity Of 98, 6% And Minimum Sensitivity Of 94, 6%, From Human Serum, Plasma Or Total Blood Samples Of Venous Or Digital Puncture, From 24 Hours Of Patient Symptoms. The Result Should Come Out Within 30 Minutes, With The Purpose Of Early Identifying Individuals With Dengue Virus Infection. You Should Track Individually Packed Test Plate (Cassette), Migration Buffer (Diluent/Reagent Solution), Disposable (Individual) Capillary Pipettes Or Contagotes For Blood And Package Leaflet Samples In Portuguese Language; Minimum Validity Of 12 Months From The Delivery Date; Packed In Reinforced And Appropriate Packaging For Product Integrity; Label With Batch Nr, Date Of Manufacture, Validity And Origin. Have Anvisa/Ms Registration. Test Storage Temperature From 2 ° C To 30 ° C., Quick Igm/Igg Antibody Detection For Dengue Virus. Quick Test Immunocromatographic Test Of Lateral Flow For Qualitative Igm And Igs Detection Separately On The Same Test Cassette, Dengue Virus Including The Four Serotypes (Dec, Den-4). The Test Should Allow Reliable Diagnosis With A Minimum Specificity Of 96, 6% And Minimum Sensitivity Of 97, 5%, Plasma Or Total Venous Or Digital Puncture Blood. The Result Should Come Out Within 30 Minutes, With The Purpose Of Identifying Individuals Who Have Or Had Infection By The Dengue Virus. You Should Track Individually Packed Test Plate (Cassette), Fast Testing Kits For Antigen Research For Sar-Cov-2. (Covid-19): Rapid Test Immunocromatographic Test For Specific Qualitative Detection Of Sar-Cov-2 Antigens (Ag), Directly From Nasopharyngeal Swab Sample And Human Oropharyngeal Swab. The Test Should Not Have Cross Reactivity With Other Viruses And Bacteria Tested, Except Sars-Cov-2 And Without Interference By Other Substances That May Be Present In The Sample. It Should Present Results Accurately: Having Sensitivity Of The Immunocromatopomatographic Test Of At Least 84, 4 % And Greater Than 99, 9 % Specificity, Providing Accurate And Rapid Results In A Maximum Of 30 Minutes. It Should Be Licensed By The Competent National Bodies, According To National And International Rules, Anvisa. Have At Least 24 Months Of Expiration, With Storage And Use Conditions At A Temperature Of 2 To 30 ° C. Fortured In Kit, Containing In Each Box: - Unit Cassettes For Testing; - Extraction Buffer; - Extraction Tube; - Dripping Lid; - Swab For Sample Collection; -Instruction Manual Of Use. Note: The Collection Should Be Through The Nasopharyngeal., Fta Test-Abs Igg For Syphilis Diagnosis. Anti-Toneponema Pallidum, If Present In The Serum, Will Bind To The Antigens Fixed On The Blade And Will Be Revealed By An Ancient Watermaglobulin Marked With Fluorescein Isotocynate.
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