Bids Are Invited For Registration Of Prices For Rapid Tests: (1) By Immunochromatographic Assay, For Qualitative, Simultaneous And Differentiated Detection Of Sars-Cov-2 Antigens And Influenza Type A And Type B (2) By Immunochromatographic Assay, For Specific Qualitative Detection Of Antigens Of Sars-Cov-2 (3) Detection Of Dengue Virus (4) Pregnancy And Urinalysis

Rapid Test, By Immunochromatographic Assay, For Qualitative, Simultaneous And Differentiated Detection Of Sars-Cov-2 And Influenza Type A And Type B Rapid Test, By Immunochromatographic Assay For Qualitative, Simultaneous And Differentiated Detection Of Sars-Cov-2 And Antigens Influenza Type A And Type B. Sample Type: Nasopharyngeal Swab And Nasal Swab Sensitivity: Sars-Cov-2: 96.52%; Influenza A: 97.44% Influenza B: 90.63%. Specificity: Sars-Cov-2: ≫99.9%; Influenza A: 100%; Influenza B: 98.82%. Presentation: Cassette. Storage: 2-30°C. Anvisa Registration. (9064), For Specific Qualitative Detection Of Sars-Cov-2 Antigensrapid Test, By Immunochromatographic Assay, For Specific Qualitative Detection Of Sars-Cov-2 Antigens In Nasopharyngeal Swab Samples. The Acquired Rapid Test Must: Present Sensitivity Greater Than 93% And Specificity Greater Than 99%; Present A Minimum Validity Period Of Six Months After Receipt Of These Tests; Enable Storage At Room Temperature; Have All The Necessary Materials For Sample Collection And Testing In Your Diagnostic Kit (Test Device, Extraction Buffer, Sterile Swab, Etc.); The Test Must Be Carried Out In A Closed System (Flask/Tube Type), To Minimize Contamination Of The Test Performer; The Swab Must Have A Shaft Of Comfortable Thickness For Use In Children And Adults, So That It Does Not Cause Bleeding, And Must Have A Leaflet With The Respective Technical Characteristics And Instructions For Use In Portuguese; Offer Technical Support And Training For Using The Test. Anvisa Registration. (9065), Rapid Test For Qualitative Detection Of Igg/Igm Antibodies (From The Fifth Day Of Symptoms) To Dengue Virus In A Human Whole Blood Sample). Containing: Test Devices, Buffer Solution, Dropper, Must Present Leaflet With The Respective Technical Characteristics And Instructions For Use In Portuguese Language And Have Anvisa Registration. Box With At Least 20 Units. (9066), Rapid Test For Qualitative Detection Of The Ns1 Antigen (From The First To The Fifth Day Of Symptoms) Of The Dengue Virus In A Human Sample Of Whole Blood, Serum Or Plasma) With Particles Of Anti-Dengue Ns1 Antibody Conjugated To Gold And Antibody -Dengue Ns1 Coated On The Device Membrane. Can Be Stored At Room Temperature Or Under Refrigeration (2-30°C). Containing: Test Devices, Must Present Leaflet With The Respective Technical Characteristics And Instructions For Use In Portuguese Language. Anvisa Registration. Box With At Least 20 Units. (9067), Pregnancy Test Reagent Strip (Beta Hcg) - Single-Step Immunochromatographic Strip Pregnancy Test, Specific For Determination Of Human Chorionic Gonadotropin (Hcg) In Urine Serum Sample With A Sensitivity Of 25 Mui/Ml . The Strips Must Be Individually Packaged In Packages With A Maximum Of 100 Strips, Containing A Desiccant Bag For Preserving The Strips And Instructions For Use. (Use Only For In Vitro Diagnosis). Anvisa Registration. (9068)