Request For Quotation A Set Of Reagents For The Automatic Biochemical Analyzer Brams Kryptor Compact Plus

A Set Of Reagents For The Quantitative Determination Of The Determination Of Pregnancy-Associated Protein A Plasma Should Quantitatively Determine The Concentration Of Papp-A (Pregnancy-Associated Protein-A Plasma) In Human Serum. The Set Must Be Compatible With The Automatic Biochemical Analyzer B•R•A•M•S Kryptor Compact Plus Installed In The Customers Laboratory. The Kit Should Consist Of: Ready-To-Use Xl-Conjugate Containing Monoclonal Antibody To Papp-A Conjugated With Xl665, Buffer, Bovine Albumin, Non-Specific Mouse Immunoglobulin And Potassium Fluoride.; Ready-To-Use K-Conjugate Containing A Monoclonal Antibody To Papp-A Conjugated With Europium Cryptate, Buffer, Bovine Albumin, Mouse Nonspecific Immunoglobulins, Potassium Fluoride; Ready-To-Use Diluent Containing Newborn Calf Serum, Sodium Azide, Preservatives: The Set Must Have A Sticker With A Barcode Containing All The Information Necessary For Registering A New Batch Of Reagents; The Number Of Tests In The Set Should Be 75; Sample Type - Serum; The Volume Of The Sample Required For The Analysis Should Be At Least 50 Μl; Incubation Time Should Be No More Than 19 Minutes; The Results Must Be Presented In Mu/L; The Stability Of The Set In The Analyzer (Stability After Opening) Must Be No Less Than 29 Days; The Principle Of Analysis Should Be A Sandwich Method; The Storage Temperature Should Be No Less Than 2°C And No More Than 8°C. The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate With The Ministry Of Health Of The Republic Of Kazakhstan. Application For Participation In The Competition, As Well As All Correspondence And Documents. Delivery Is Carried Out By The Supplier At His Own Expense. Packaging Of 75 Tests, Die For Dilution. Tablets Must Be Intended For Diluting Samples On The B·R·A·H·M·S Kryptor Compact Plus Device; The Number Of Tablets In The Package Must Be At Least 30 Tablets; Tablets For Dilution Should Have 24 Wells In Each; There Should Be 30 Adhesive Films In The Set; Tablets Must Remain Stable For At Least 29 Days; The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate In The Ministry Of Health Of The Republic Of Kazakhstan. The Application For Participation In The Competition, As Well As All Correspondence And Documents Related To The Application For Participation In The Competition, Are Drawn Up And Provided In Kazakh Or Russian At The Choice Of The Potential Supplier. Delivery Is Carried Out By The Supplier At His Own Expense. Packaging Of 30 Dies, The Calibrator For Plasma Pregnancy-Related Protein A Should Be Used To Correct The Standard Curve Stored In B·R·A·H·M·S Kryptor Compact Plus. The Calibrator Must Be Compatible With The Automatic Biochemical Analyzer B•R•A•M•S Kryptor Compact Plus Installed In The Customers Laboratory. The Package Should Consist Of: Papp-A/Prombp Complex Of Human Origin, Human Blood Serum And Sodium Azide; The Sticker With The Barcode Must Contain Information About The Batch Of The Calibrator, Including The Concentration Value. The Number Of Bottles In The Package Should Be 6; The Stability Of The Calibration Must Be At Least 15 Days; The Principle Of Analysis Should Be A Sandwich Method; The Storage Temperature Should Be No Less Than 2°C And No More Than 8°C. The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate In The Ministry Of Health Of The Republic Of Kazakhstan. Application For Participation In The Competition, Delivery Is Carried Out By The Supplier At Its Own Expense. Packaging 6X1 Fl, The Buffer Should Be A Concentrate Of Phosphate-Salt Buffer Solution (Pbs), Which Should Be Intended For The Preparation Of Systemic Fluid; The Buffer Must Be Compatible With The Automatic Biochemical Analyzer B•R•A•M•S Kryptor Compact Plus Installed In The Customers Laboratory; The Buffer Should Be In The Form Of A Powder; The Package Must Contain At Least 5 Sachets; Each Bag Must Be At Least 65 Grams; A Bag Of Powder Should Be Diluted In The Ratio Of 1 Bag To 5 Liters Of Distilled Water; The Composition Of The Powder Should Contain Potassium Phosphate In A Concentration Of At Least 25%, Sodium Phosphate In A Concentration Of At Least 50% And Sodium Chloride In A Concentration Of At Least 50%; Ph Should Be In The Range From 6.8 To 7.0; ; A Bag Of Powder Should Be Diluted In The Ratio Of 1 Bag To 5 Liters Of Distilled Water; The Buffer Solution Should Remain Stable For At Least 15 Days; The Storage Temperature Should Be No Less Than 18°C ​​And No More Than 30°C. The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate In The Ministry Of Health Of The Republic Of Kazakhstan. The Application For Participation In The Competition, As Well As All Correspondence And Documents Related To The Application For Participation In The Competition, Are Drawn Up And Provided In Kazakh Or Russian At The Choice Of The Potential Supplier. Delivery Is Carried Out By The Supplier At His Own Expense. Packaging 5X65 G, A Set Of Reagents For Determining The Free Beta Subunit Of Human Chorionic Gonadotropin Should Quantitatively Determine The Concentration Of Free Β-Hcg (Free Beta Subunit Of Human Chorionic Gonadotropin) In Human Blood Serum. The Set Must Be Compatible With The Automatic Biochemical Analyzer B•R•A•M•S Kryptor Compact Plus Installed In The Customers Laboratory. The Kit Should Consist Of: Ready-To-Use Xl-Conjugate Containing Monoclonal Antibody To Free Β-Hcg Conjugated With Xl-665, Buffer, Bovine Albumin, Non-Specific Mouse Immunoglobulins, Potassium Fluoride; Ready-To-Use K-Conjugate Containing A Monoclonal Antibody To Free Β-Hcg Conjugated With Europium Cryptate, Buffer, Bovine Albumin, Mouse Nonspecific Immunoglobulins, Potassium Fluoride; Ready-To-Use Diluent Containing Newborn Calf Serum, Preservatives: The Kit Must Have A Sticker With A Barcode Containing All The Information Necessary For Registering A New Batch Of Reagents; The Number Of Tests In The Set Should Be 75; Sample Type - Serum; The Volume Of The Sample Required For The Analysis Should Be At Least 26 Μl; Incubation Time Should Be No More Than 19 Minutes; The Results Must Be Presented In Ng/Ml; The Stability Of The Set In The Analyzer (Stability After Opening) Must Be No Less Than 29 Days; The Principle Of Analysis Should Be A Sandwich Method; The Storage Temperature Should Be No Less Than 2°C And No More Than 8°C. The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate In The Ministry Of Health Of The Republic Of Kazakhstan. Delivery Is Carried Out By The Supplier At His Own Expense., A Set Of Controls For Prenatal Screening Must Be Used To Control The Quality Of The Analysis In The B•R•A•M•S Kryptor Compact Plus Device Installed In The Customers Laboratory; The Package Should Have Three Levels Of Control, 2 Vials Per Level; Each Vial Should Contain A Lyophilized Mixture Of Such Human Antigens As Afp, Free Β-Hcg And Papp-A, Human Blood Serum And A Preservative; A Sticker With A Barcode Must Contain Information About The Batch Of Controls, In Particular, The Values ​​Of The Target Concentrations, The Obtained Values ​​Of The Standard Deviations, And The Acceptable Concentration Ranges; The Package Must Contain Self-Adhesive Labels With A Bar Code Of 32 For Each Control; The Number Of Bottles In The Package Should Be 6; The Principle Of Analysis Should Be A Sandwich Method; The Storage Temperature Should Be No Less Than 2°C And No More Than 8°C. The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate In The Ministry Of Health Of The Republic Of Kazakhstan. The Application For Participation In The Competition, As Well As All Correspondence And Documents Related To The Application For Participation In The Competition, Are Drawn Up And Provided In Kazakh Or Russian At The Choice Of The Potential Supplier. Delivery Is Carried Out By The Supplier At His Own Expense. Packing 3X2 Fl, Die For Reactions. Tablets Must Be Intended For Incubation Of Samples And Reagents, As Well As For Measuring Fluorescence On The B·R·A·H·M·S Kryptor Compact Plus Device.; The Number Of Tablets In The Package Must Be At Least 60 Tablets; Reaction Tablets Must Have 96 Wells In Each; There Should Be 60 Adhesive Films In The Set; Tablets Must Remain Stable For At Least 7 Days; The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate In The Ministry Of Health Of The Republic Of Kazakhstan. The Application For Participation In The Competition, As Well As All Correspondence And Documents Related To The Application For Participation In The Competition, Are Drawn Up And Provided In Kazakh Or Russian At The Choice Of The Potential Supplier. Delivery Is Carried Out By The Supplier At His Own Expense. Packaging Of 60 Dies, The Solution 4 Solution Should Be Intended For Flushing The B·R·A·H·M·S Kryptor Compact/Kryptor Compact Plus Liquid System. The Solution Must Be Compatible With The Automatic Biochemical Analyzer B•R•A•M•S Kryptor Compact Plus Installed In The Customers Laboratory; There Should Be At Least 4 Ready-To-Use Bottles Of 55 Ml In The Package; The Solution Must Contain Sodium Hydroxide At Least < 2.0%; The Solution Should Remain Stable For At Least 29 Days; The Storage Temperature Should Be No Less Than 2°C And No More Than 8°C. The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate In The Ministry Of Health Of The Republic Of Kazakhstan. The Application For Participation In The Competition, As Well As All Correspondence And Documents Related To The Application For Participation In The Competition, Are Drawn Up And Provided In Kazakh Or Russian At The Choice Of The Potential Supplier. Delivery Is Carried Out By The Supplier At His Own Expense. Packaging 4X55 Ml., The Calibrator For The Free Beta Subunit Of Human Chorionic Gonadotropin Should Be Used To Correct The Standard Curve Stored In B·R·A·H·M·S Kryptor Compact Plus. The Calibrator Must Be Compatible With The Automatic Biochemical Analyzer B•R•A•M•S Kryptor Compact Plus Installed In The Customers Laboratory. The Packaging Should Consist Of: Ready-To-Use Highly Purified Free Β-Hcg, Serum Of Newborn Calves And Preservatives; The Sticker With The Barcode Must Contain Information About The Batch Of The Calibrator, Including The Concentration Value. The Number Of Bottles In The Package Should Be 6; The Stability Of The Calibration Should Be No Less Than 15 Days; The Principle Of Analysis Should Be A Sandwich Method; The Storage Temperature Should Be No Less Than 2°C And No More Than 8°C. The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate With The Ministry Of Health Of The Republic Of Kazakhstan. The Application For Participation In The Competition, As Well As All Correspondence And Documents Related To The Application For Participation In The Competition, Are Drawn Up And Provided In Kazakh Or Russian At The Choice Of The Potential Supplier. Delivery Is Carried Out By The Supplier At His Own Expense. 6X1 Fl, The Solution 3 Solution Should Be Intended For Flushing The B·R·A·H·M·S Kryptor Compact/Kryptor Compact Plus Liquid System. The Solution Must Be Compatible With The Automatic Biochemical Analyzer B•R•A•M•S Kryptor Compact Plus Installed In The Customers Laboratory; There Should Be At Least 4 Ready-To-Use Bottles Of 30 Ml Each In The Package; The Solution Should Contain Sodium Hydroxide Not Less Than <0.5% And Sodium Hypochlorite Not Less Than <5.0%.; The Solution Should Remain Stable For At Least 29 Days; The Storage Temperature Should Be No Less Than 2°C And No More Than 8°C. The Product Release Date Must Be No Earlier Than 2023; The Supplier Provides Documents Confirming The Compliance Of The Supplied Goods With The Requirements Established By Technical Regulations, Provisions Of Standards Or Other Documents In Accordance With The Legislation Of The Republic Of Kazakhstan, Including A Registration Certificate In The Ministry Of Health Of The Republic Of Kazakhstan. The Application For Participation In The Competition, As Well As All Correspondence And Documents Related To The Application For Participation In The Competition, Are Drawn Up And Provided In Kazakh Or Russian At The Choice Of The Potential Supplier. Delivery Is Carried Out By The Supplier At His Own Expense. Packaging 4X30 Ml