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| 1 | Item Wise BoQ BoQ_Ver3.0 Item Wise Normal INR Only INR Select, Excess (+), Less (-) Tender Inviting Authority: Superintendent, PBM AG of Hospital,Bikaner Name of Work: Supply of various type of test kits and consumables for Microbiology Department Contract No: ENIB No 27 (2025-26) Bidder Name : PRICE SCHEDULE(This BOQ template must not be modified/replaced by the bidder and the same should be uploaded after filling the relevent columns, else the bidder is liable to be rejected for this tender. Bidders are allowed to enter the Bidder Name and Values only ) NUMBER # TEXT # TEXT # NUMBER # TEXT # NUMBER NUMBER TEXT TEXT # NUMBER # TEXT# TEXT # NUMBER # NUMBER NUMBER NUMBER NUMBER TEXT TEXT NUMBER NUMBER NUMBER NUMBER TEXT TEXT NUMBER NUMBER NUMBER NUMBER TEXT TEXT NUMBER NUMBER NUMBER NUMBER TEXT TEXT NUMBER NUMBER NUMBER NUMBER TEXT TEXT NUMBER NUMBER NUMBER # NUMBER # TEXT TEXT NUMBER # NUMBER # DATE NUMBER # NUMBER # TEXT # S.No NAME OF ITEMS Item Code / Make Quantity Pack Size Estimated Rate MRP Addition / Deduction Addition / Deduction Values Currency Convertion against each Item Quoted Currency in INR / Other Currency BASIC RATE In Figures To be entered by the Bidder with out GSTRs. P Excise Duty GST in Figures to be entered by the Bidder Rs. Freight Charges ( Unloading & Stacking) Any Other Taxes/Duties/Levies Other Taxes 2 IIIrd Party i.e DGS&D / RITES etc Inspection Charges @0.34%+Service Tax Less for Cenvat Credit,if any respect of Supplies Under full Excise Duty Category TOTAL AMOUNT Without GST TOTAL AMOUNT With GST TOTAL AMOUNT In Words |
| 2 | Dengue Rapid test for detecting NS1 antigen & IgG & IgM antibody.• Should be capable of detecting dengue infection from day-1 & should be preferably capable of detecting all 04 serotypes of Dengue virus. • Should have High sensitivity and specificity and positive Control. |
| 3 | RA (Latex Agglutination test)- • Should be preferably CE marked/certified.• Reagent should be calibrated against WHO international standard.• Latex particles coated with purified human gamma globulin.• Should have with positive Control. |
| 4 | CRP (Latex Agglutination test)• Should be preferably CE marked/certified.• Latex particles coated with anti-human CRP.• Should have with positive Control. |
| 5 | ASO(Latex Agglutination test)• Should be preferably CE marked/certified.• Latex particles coated with purified streptolysin O. |
| 6 | HBsAg Rapid test • Should be capable of detecting preferably all subtypes of HBsAg.• Lateral Flow through technology.• Antigen sensitivity should be around 0.5ng/ml.• Should have with Positive Control.• Note:- Sensitivity & Specificity should preferably be >99% |
| 7 | Anti HCV Rapid test-• Lateral Flow through technology.• Should be capable of detecting preferably all subtypes of HCV.• Note:- Sensitivity & Specificity should preferably be >99% |
| 8 | Rapid Malaria antigen card test • Based on pLDH for Pv & HRP-2 detection for Pf i.e. • Should be Pv & Pf specific. • Should preferably be developed according to WHO guidelines & Hence approved. |
| 9 | Widal slide test• Stabilized reagent for long shelf life (18 months or more at 2 to 8 oC.)• Available in 5ml vials separately Salmonella O, Salmonella H, Salmonella A (H) & Salmonella B(H).• Should be preferably CE marked/certified. |
| 10 | UPT Card test |
| 11 | RPR Slide test• Should be preferably CE marked/certified.• Ready to use reagent.• Positive control provided with kit.• Stabilized reagent for long shelf life (18 months or more)• Specimen can be plasma/Serum can be used without heat inactivation.• Preferably calibrated to WHO reference serum for serodiagnostic test for treponemal infection. |
| 12 | Brucella (Rose Bengal Test)• Should be preferable CE marked/ certified.• Positive control should preferably be supplied along with kit.• More than 12 months reagent shelf life at 2 to 8 degree c. |
| 13 | Scrub Typhus Rapid card Test• Long Shelf Life (more than 18 months at 2-30 oC)• Lateral Flow through technology.• Sensitivity & Specificity should preferably be >99% |
| 14 | Dengue NS1 ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 15 | Dengue IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 16 | Dengue IgG ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 17 | Scrub typhus IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 18 | Scrub typhus IgGELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 19 | HAV IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 20 | HEV IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 21 | Brucella IgG ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 22 | Brucella IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 23 | Chikungunya Rapid card test. • Based in sandwich immunoassay principle.• High sensitive & Specific.• More than 12 months shelf life. |
| 24 | Chikungunya IgM ELISA Test.• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 25 | HBsAgELISA Test.• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 26 | HCVELISA Test.• 4th Generation should be able to detect antigen of core/ antibody to core, NS3, NS4, NS Region.• Must be approved from DGHS/CDSCO/NABL/NIB (Must Attach Certificate)• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 27 | 4th Generation, HIV ELISA Test kits for 96 test• 4th Generation HIV should be able for the detection of HIV p24 Antigen and antibodies to HIV – 1 (including subgroups) and HIV – 2 in Human serum/plasma.• Sensitivity should be 100% • Use of envelop antigens gp 41 & C terminus of gp 120 for HIV-1 & gp 36 for HIV-2.• Must be approved from DGHS/ CDSCO/NABL/NACO/NIB for use in Blood Centre. (Must attach certificate)• |
| 28 | 4thGeneration, HIV Rapid Test kits08. 4th Generation HIV should be able for the detection of HIV p24 Antigen and antibodies to HIV – 1 and HIV – 2.09. Sensitivity should be 100% 10. Use of envelop antigen gp-41 & C-terminus of g[ 120 for HIV-I & gp-36 for HIV-211. Test should be in single step procedure.12. Total time taken for test (including result) within 10 to 20 minutes.13. Whole Blood & Plasma (Both) may be used as sample.Must be approved from DGHS/ CDSCO/NABL/NACO/NIB for use in Blood Centre. (Must attach certificate) |
| 29 | 4th Generation HbsAg ELISA for the detection of surface Antigens of HBV (96 Test kits)• Sensitivity& Specficity should be 100% • Must be able to detect less then 0.1 Nano gm./ ml.Must be approved from DGHS/CDSCO/NABL/NACO/NIB (Must attach certificate) |
| 30 | Syphilis Rapid Strip/ Card test |
| 31 | LEPTOSPIROSIS IgG ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit |
| 32 | LEPTOSPIROSIS IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 33 | LEPTOSPIROSIS RAPID CARD TEST |
| 34 | FUNGAL MARKER 1-3 BETA-D-GLUCAN ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit |
| 35 | FUNGAL MARKER GALACTOMANNAN ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 36 | ANTI ECHINOCOCCAL IgG ANTIBODY ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 37 | TOXOPLASMA IgG ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 38 | TOXOPLASMA IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 39 | RUBELLA IgG ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 40 | RUBELLA IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 41 | CMV IgG ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 42 | CMV IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 43 | HSV IgG ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 44 | HSV IgM ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 45 | Salmonella typhi Rapid Card Test for detecting both IgG & IgM antibody.• Long shelf life (18 months or more at 2 to 30 oC.)• Should have High sensitivity and specificity and positive Control. |
| 46 | SARS CoV-2 Antibody Rapid Card Test |
| 47 | SARS CoV-2 Antibody ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 48 | Anti – HBsAntibody ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 49 | Anti HBc IgM Antibody ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 50 | HBe Antigen ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 51 | Anti HBe Antibody ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 52 | EBV IgM Antibody ELISA Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 53 | Panfungal DNA Qualitative PCR Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit.• The kit should be compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same. |
| 54 | Fungal Qualitative PCR for Mucormycosis • Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit.• The kit should be compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same. |
| 55 | HIV Quantitative PCR Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit.• The kit should be compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same. |
| 56 | EBV Quantitative PCR Test• QC certificate to be enclosed with each kit.• The kit should be an in vitro nucleic acid amplification assay for the qualitative and quantitative detection of Epstein-Barr Virus DNA from clinical samples using compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same.• The limit of detection of the kit should be 1.5 IU/µl.• Kit should have CE/IVD certificate. |
| 57 | HSV Quantitative PCR Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit.• The kit should be compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same. |
| 58 | HPV Quantitative PCR Test• QC certificate to be enclosed with each kit.• The kit should be compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same.• Kit should be TaqMan Probe-Based Real-Time PCR Assay.• Kit should be able to do detection and simultaneously genotyping of 14 High Risk HPV Genotypes• (16/18/31/33/35/39/45/51/52/56/58/59/66 and 68).• Kit should beBased on E6/E7 oncoproteins which mediate the development of cervical cancer.• Kit should have Endogenous internal control DNA which allows excluding unreliable results.• Kit should have CE/IVD certificate. |
| 59 | CMV Quantitative PCR Test• QC certificate to be enclosed with each kit.• The kit should be an in-vitro nucleic acid amplification assay for the detection and quantification of cytomegalovirus (CMV) specific DNA in human plasma samples compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same.• The Kit should be calibrated with 1st WHO International standard for CMV for Nucleic acid amplification techniques.• The Kit should have higher sensitivity and specificity compared with other diagnostic methods such as serological assays and culture methods.• Detection limit of this assay is 50 IU/ml.• No cross- reactivity with other pathogenic virus, bacteria or fungi.• Internal control included in the kit• Kit should have CDSCO & CE/IVD certificate. |
| 60 | CMV (DNA) Qualitative PCR Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit.• The kit should be compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same. |
| 61 | HSV 1/2 (DNA) Qualitative PCR Test• QC certificate to be enclosed with each kit.• The kit should be an in vitro nucleic acid amplification assay for the qualitative single tube detection of Herpes Simplex Virus-1 (HSV-1) and Herpes Simplex Virus-2 (HSV-2) from clinical samples compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same.• Kit should be able to do detect HSV 1= 0.5 copies/µl and HSV 2= 0.5 copies/µl.• Kit should have CE/IVD certificate. |
| 62 | Chlamydia Trachomatis Qualitative PCR Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit.• The kit should be compatible with multiple extraction and PCR systems especially CFX96™ Real-Time PCR Detection System (Bio-Rad), CFX96™ Deep Well Real-Time PCR Detection System (Bio-Rad), QuantStudio™ 5 Real-Time PCR (Applied Biosystem) etc and should have documented proof for the same. |
| 63 | HBsAg Rapid test • Should be capable of detecting preferably all 14 mutants of HBsAg.• Lateral Flow through technology.• Analyticalsensitivity should be around 0.1 IU/ml.• Should have with Positive Control.• Should be WHO pre-qualified and NIB Evaluated.• Should be preferably CE marked/certified.• Note:- Sensitivity & Specificity should preferably be >99% |
| 64 | GLASS SLIDE (75 X 25mm) thickness 1.45 mm |
| 65 | COVER SLIP 22 x 22 mm thickness 0.13 -0.16 |
| 66 | COVER SLIP 22 x 60 mm NO.0 English Glass |
| 67 | GLASS PETRIDISH Autoclavable 150mm X 20mm |
| 68 | PLASTIC PETRIDISH Autoclavable 100 mm X 17mm |
| 69 | PLASTIC PETRIDISH disposable sterile 100 mm X 17mm |
| 70 | GLASS PETRIDISH Autoclavable 100mm X 17mm |
| 71 | GLASS TUBES( with rim) 6 x1 inches 20ml Capacity |
| 72 | GLASS TUBES( with rim) 5 x1 inches 10ml Capacity |
| 73 | GLASS TUBES( with rim) 4 x 0.5 inches 5ml Capacity |
| 74 | YELLOW TIPS (20-200 ul) |
| 75 | BLUE TIPS upto 1000 ul |
| 76 | TEST TUBE STAND OF HARD PLASTIC/ STEEL-• 96 vials, 12mm x 75 mm / 100 mm test tubes• 12 places for 25 mm diameter test tubes• Stand for centrifuse tubes 1.5 ml, 2.2 ml & 2.7ml capacity• Stand for vials 5 ml vial with 24 vial holding capacity, hole size 14mm• 2 shelves folding stand, 18 tubes holding capacity, hole size 18 mm.• 3 shelves folding stand, 18 tubes holding capacity, hole size 16 mm |
| 77 | UNIVERSAL STERILE CONTAINER SCREW CAP 30ml capacity (Plastic) |
| 78 | MICROPIPETTE FIXED 20ul• The Lightest Manual Pipette• Fully Autoclavable at 121 °C• Rugged/Robust Construction & Durability• Universal Tip Compatibility with all brands.• Soft touch tip ejector.• Easy to mentle – dis-mentle pipette.• With narrow head nozzle. |
| 79 | MICROPIPETTE FIXED 50ul• The Lightest Manual Pipette• Fully Autoclavable at 121 °C• Rugged/Robust Construction & Durability• Universal Tip Compatibility with all brands.• Soft touch tip ejector.• Easy to mentle – dis-mentle pipette.• With narrow head nozzle. |
| 80 | MICROPIPETTE FIXED 100ul• The Lightest Manual Pipette• Fully Autoclavable at 121 °C• Rugged/Robust Construction & Durability• Universal Tip Compatibility with all brands.• Soft touch tip ejector.• Easy to mentle – dis-mentle pipette.• With narrow head nozzle. |
| 81 | MICROPIPETTE VARIABLE 5-50ul• The Lightest Manual Pipette• Fully Autoclavable at 121 °C• Rugged/Robust Construction & Durability• Universal Tip Compatibility with all brands.• Advance Volume Gearing (AVG) System to avoid sudden change in gearing.• 3-4 digit display in pipetting• Soft touch tip ejector.• Easy to mentle – dis-mentle pipette.• Large ergonomics display• With narrow head nozzle. |
| 82 | MICROPIPETTE VARIABLE 10-100ul• The Lightest Manual Pipette• Fully Autoclavable at 121 °C• Rugged/Robust Construction & Durability• Universal Tip Compatibility with all brands.• Advance Volume Gearing (AVG) System to avoid sudden change in gearing.• 3-4 digit display in pipetting• Soft touch tip ejector.• Easy to mentle – dis-mentle pipette.• Large ergonomics display• With narrow head nozzle. |
| 83 | 01. MICROPIPETTE VARIABLE 100-1000ul• The Lightest Manual Pipette• Fully Autoclavable at 121 °C• Rugged/Robust Construction & Durability• Universal Tip Compatibility with all brands.• Advance Volume Gearing (AVG) System to avoid sudden change in gearing.• 3-4 digit display in pipetting• Soft touch tip ejector.• Easy to mentle – dis-mentle pipette.• Large ergonomics display• With narrow head nozzle. |
| 84 | ANTISEPTIC HAND WASH |
| 85 | TISSUE PAPER ROLL Premium Extra Large with 425 sheets (2 Ply ) size 95 x 110 mm. |
| 86 | DRAYERS TUBES |
| 87 | FELIX TUBES |
| 88 | MARKER Fine TipBLACK/RED/BLUE |
| 89 | GLASS MARKING PENCILWHITE/BLACK |
| 90 | WHATMAN FILTER PAPER grade 1 |
| 91 | POSTMARTUM GLOVES (7.5 inches) |
| 92 | GLASS BOTTLE WITH ALUMINUM CAP FOR L.J. MEDIUM (80mm x 20 mm) |
| 93 | ANTISEPTIC HAND WASHTISSUE PAPER ROLL Premium Extra Large with 425 sheets (2 Ply ) size 95 x 110 mm. DRAYERS TUBESFELIX TUBESMARKER Fine TipBLACK/RED/BLUEGLASS MARKING PENCILWHITE/BLACKWHATMAN FILTER PAPER grade 1POSTMARTUM GLOVES (7.5 inches)GLASS BOTTLE WITH ALUMINUM CAP FOR L.J. MEDIUM (80mm x 20 mm) |
| 94 | Histoplasma Capsulatum Antigen Detection Test• Should be preferable CE marked/ certified.• QC certificate to be enclosed with each kit. |
| 95 | Stool occult blood rapid test.Specification :-• Rapid immunochemical fecal occult blood (IFOBT) kits, a 50-test (507) kit specification:• Method: Immunochemical, Lateral Flow (colloidal gold, double antibody sandwich).• Result Time: 5-15 minutes.• Accuracy/Agreement: Generally >98-99% compared to reference methods.Specificity: High for human hemoglobin; typically not affected by diet (no restriction needed). |
| 96 | Measles IgM ELISA Specification :-• Qualitative/quantitative test for acute measles, using serum/plasma on antigen-coated microplates, detec antibodies with high sensitivity (>98%) and specificity (>99%), utilizing ready-to-use reagents.Key Specifications & Components• Target: IgM antibodies to Measles Virus in human serum/plasma.• Principle: Indirect ELISA.• Performance: High sensitivity (>98%) and specificity (>99%) for acute infection diagnosis.• Controls: Include positive, negative, and cutoff calibrators for valid runs.• Sample Handling: Serum/plasma.• Example Specification (from procurement/technical docs)• Sensitivity: >98%.• Specificity: >99%,• Kit Contents: 96 tests. |
| 97 | CL detect Rapid test • Should be able to detect Leishmania Ag from skin lesions.• Immunochromatographic test assay.Sensitivity & Specificity: > 90% & 95% Total in Figures 0.0 0.0 0.0 67.0 0.0 0.0 0.0 0.0 0.0 INR Zero Only 4.0 Construction of chamber for 100mm sluice plates item5 10.0 Nos Quoted Rate in Figures Select % 0.0 0.0 Zero Only Quoted Rate in Words Please Enable Macros to View BoQ information |
