Poland - Laboratory reagents

Description

1. The subject matter of the order is successive supplies of reagents along with lease of analyzers for 36 months in the scope and subject matter specified in the price form (Annex No. 1A to the SWZ) meeting the technical and quality requirements, divided into parts (packages):1) Package No. 1 - Supply of reagents for immunodiagnostics and biochemistry together with the lease of an analyzer for biochemistry and a centrifuge2) Package No. 2 - Supply of RKZ reagents, oximetry, metabolites, electrolytes together with the lease of two analyzers3) Package No. 3 - Supply of tests and laboratory reagents2. For a detailed description of the subject matter of the order, please refer to Appendix No. 1A to the SWZ - Price Form and Appendix No. 1B to the SWZ - Technical Conditions.
The subject matter of the order is successive supply for 36 months of reagents with lease of analyzers in the scope and subject matter specified in the price form (Annex No. 1A to SWZ) meeting the technical and quality conditions, divided into parts (packages):1) Package No. 1 - Supply of reagents for immunodiagnostics and biochemistry with lease of an analyzer for biochemistry and centrifuge2. For a detailed description of the subject matter of the contract, please refer to Annex No. 1A to the SWZ - Price Form and Annex No. 1B to the SWZ - Technical Conditions. (3) The Contractor shall enter in the price form in the columns "Catalog number, trade name and manufacturer" the trade name of the offered product, the name of its manufacturer and catalog number.4. The offered reagents must be authorized for marketing and use in the Republic of Poland in accordance with the Act of April 7, 2022 on medical devices (Journal of Laws item 974 and/or the Regulation of the Minister of Health on essential requirements and conformity assessment procedures for medical devices (Journal of Laws 2016 item 211). The Contractor will declare its ability to provide, at any request of the Purchaser, a CE declaration of conformity and/or a certificate of conformity issued by a notified body and/or registration of the President of the Office for Registration of Medical Products, Medical Devices and Biocidal Products. The Contractor shall also declare possession of Material Safety Data Sheets - for reagents having substances classified as hazardous in their composition, in accordance with the Ordinance of the Minister of Health of August 10, 2012 on the criteria and method of classification of chemical substances and their mixtures (i.e. Journal of Laws of 2015, item 208) and provide them to the Ordering Party within 7 days after signing the contract.5.If the Contractor offers a given product in a package containing a different quantity than that entered in the price form, the number of packages should be recalculated accordingly, rounding up to the nearest whole number. In order to check the correctness of the conversion, the Purchaser asks the Contractors to indicate the fact of converting the number of packages, e.g. by bold text6. Important!!! Offered analyzers, reagents, controls and consumables, must come from one manufacturer and constitute a complete analytical system 1. The subject matter of the order is successive supply for 36 months of reagents together with lease of analyzers in the scope and subject matter specified in the price form (Annex No. 1A to the SWZ) meeting the technical and quality conditions, divided into parts (packages):2) Package No. 2 - Supply of RKZ reagents, oximetry, metabolites, electrolytes together with lease of two analyzers2. For a detailed description of the subject matter of the contract, please refer to Appendix No. 1A to the SWZ - Price Form and Appendix No. 1B to the SWZ - Technical Conditions. (3) The Contractor shall enter in the price form in the columns "Catalog number, trade name and manufacturer" the trade name of the offered product, the name of its manufacturer and catalog number.4. The offered reagents must be authorized for marketing and use in the Republic of Poland in accordance with the Act of April 7, 2022 on medical devices (Journal of Laws item 974 and/or the Regulation of the Minister of Health on essential requirements and conformity assessment procedures for medical devices (Journal of Laws 2016 item 211). The Contractor will declare its ability to provide, at any request of the Purchaser, a CE declaration of conformity and/or a certificate of conformity issued by a notified body and/or registration of the President of the Office for Registration of Medical Products, Medical Devices and Biocidal Products. The Contractor shall also declare possession of Material Safety Data Sheets - for reagents having substances classified as hazardous in their composition, in accordance with the Ordinance of the Minister of Health of August 10, 2012 on the criteria and method of classification of chemical substances and their mixtures (i.e. Journal of Laws of 2015, item 208) and provide them to the Ordering Party within 7 days after signing the contract.5.If the Contractor offers a given product in a package containing a different quantity than that entered in the price form, the number of packages should be recalculated accordingly, rounding up to the nearest whole number. In order to check the correctness of the conversion, the Purchaser asks the Contractors to indicate the fact of converting the number of packages, e.g. by bold text6. Important!!! Offered analyzers, reagents, controls and consumables, must come from one manufacturer and constitute a complete analytical system 1. The subject of the order are successive supplies of reagents for a period of 36 months, together with the lease of analyzers in the scope and subject matter specified in the price form (Annex No. 1A to SWZ) meeting the technical and quality conditions, divided into parts (packages):3) Package No. 3 - Supplies of tests and laboratory reagents2. A detailed description of the subject matter of the order is contained in Appendix No. 1A to the SWZ - Price Form and in Appendix No. 1B to the SWZ - technical conditions. (3) The Contractor shall enter in the price form in the columns "Catalog number, trade name and manufacturer" the trade name of the offered product, the name of its manufacturer and catalog number.4. The offered reagents must be authorized for marketing and use in the Republic of Poland in accordance with the Act of April 7, 2022 on medical devices (Journal of Laws item 974 and/or the Regulation of the Minister of Health on essential requirements and conformity assessment procedures for medical devices (Journal of Laws 2016 item 211). The Contractor will declare its ability to provide, at any request of the Purchaser, a CE declaration of conformity and/or a certificate of conformity issued by a notified body and/or registration of the President of the Office for Registration of Medical Products, Medical Devices and Biocidal Products. The Contractor shall also declare possession of Material Safety Data Sheets - for reagents having substances classified as hazardous in their composition, in accordance with the Ordinance of the Minister of Health of August 10, 2012 on the criteria and method of classification of chemical substances and their mixtures (i.e. Journal of Laws of 2015, item 208) and provide them to the Ordering Party within 7 days after signing the contract.5.If the Contractor offers a given product in a package containing a different quantity than that entered in the price form, the number of packages should be recalculated accordingly, rounding up to the nearest whole number. In order to check the correctness of the conversion, the Purchaser asks the Contractors to indicate the fact of converting the number of packages, e.g. by bold text6. Important!!! Offered analyzers, reagents, controls and consumables, must come from one manufacturer and constitute a complete analytical system

Opportunity closing date

28 November 2023

Value of contract

to be confirmed