Bids Are Invited For Price Registration For Acquisition Of Kits For Pcr Detection Of Cmv, Bkv And Multiplex ... in Brazil

Work Detail

Kit, For Detection Of Cytomegalovirus (Cmv) By Pcr In Real Time In Whole Blood Or Plasma Samples; With Primer And Fluorescent Probe In A Single Molecule. The Kit Must Come Accompanied By All Controls (Positive Or Standard, Negative And Internal) And A Mix Of All Reagents Necessary For The Development Of The Reaction (For Example Of Mgcl2, Dnpts, Dna Polymerase, Glycerol, Tris Hci, Edta, Among Others) And Reverse Transcriptase. Must Show Results Within 120 Minutes. The Product Must Be Packed In Reinforced Packaging And Stored At The Temperature Indicated By The Manufacturer. Must Be Registered With The Ministry Of Health And Certificate Of Origin. Packaging In Kits For A Minimum Of 96 Tests, With Product Identification Data, Manufacturers Brand, Batch Number, Manufacturing Date And Expiration Date., For Detection Of Poliomavirus (Bkv) By Pcr In Real Time In Urine Or Plasma Samples; With Primer And Fluorescent Probe In A Single Molecule. The Kit Must Come Accompanied By All Controls (Positive Or Standard, Negative And Internal) And A Mix Of All The Reagents Necessary For The Development Of The Reaction (For Example Of Mgcl2, Among Others). Must Show Results Within 120 Minutes. The Product Must Be Packed In Reinforced Packaging And Stored At The Temperature Indicated By The Manufacturer. Must Be Registered With The Ministry Of Health And Certificate Of Origin. Packaging In Kits For A Minimum Of 96 Tests, With Product Identification Data, Date Of Manufacture And Expiration Date., Test, Multiplex Qpcr Type In A Single Panel With At Least 21 Pathogens For Qualitative Detection Of Viral Nucleic Acid Including Human Adenovirus (Hadv), Human Metapneumovirus A (Hmpva), Influenza A (Flua), Influenza B (Flub), Influenza A (H1n1), Human Parainfluenza And Respiratory Syncytial Virus (Hrsva) In Biological Samples Of Human Origin. Detection System Must Include All Reagents For Reverse Transcription (One Step System), Amplification, Controls And Reaction Calibrators. Must Be Registered With The Ministry Of Health And Certificate Of Origin. Packaging With Product Identification Data, Multiplex Qpcr Type, In A Single Panel With At Least 11 Pathogens For Qualitative Detection Of Viral Nucleic Acid Including Herpes Simplex 1 And 2 (Hsv1 And Hsv2), Varicella Zoster Virus (Vzv), Erythrovirus B19 (B19), Human Herpesvirus 6 And 7 (Hhv6 And Hhv7) In Biological Samples Of Human Origin. Detection System Must Include All Reagents For Reverse Transcription (One Step System), 12/18/2025 - 18:31:06

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