Purchase and delivery of defibrillators, fire brigade equipment, tanker truck and hydraulic spreader for civil protection and civil defense needs under the Civil Protection and Civil Defense Program for 2025-2026

… his own expense. 4.The offered equipment should meet all safety and energy consumption requirements set out in the law in force in Poland, should be allowed to be placed on the market on the territory of the Republic of Poland, should comply with the relevant technical standards, have certificates allowing for use in the European Union and is marked in accordance with the applicable regulations (if applicable). 5.The Contractor will provide a guarantee for individual equipment, as indicated in Annex 5.1-5.4 to the FTZ, the warranty period is counted from the date of signing the delivery and acceptance protocol without any comments. 6.Products classified as medical devices (part II) And the subject of the contract) must meet the requirements of the Act of 7 April 2022 on medical devices (Journal of Laws of 2022, No. Journal of Laws 2024, item 1620 as amended) and the implementing acts referred to therein and Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (OJ U. EU. L. of 2017, No 117, p. 1 as amended; hereinafter referred to as: ‘Regulation 2017/745’), as well as bear the CE marking and the EU declaration of conformity or the declarations referred to in Article 22(1)(b) and (c) of Regulation (EU) 2017/745. 1 or 3 of Regulation 2017/745 and labels and instructions for use in Polish or English, except for patient information, which shall be provided in Polish or expressed by harmonised symbols or recognisable codes. 7.The subject of the contract will be marked in accordance with the requirements for release for free circulation to the extent defining the subject of the contract. (applies to medical devices) In accordance with Art. 4 EU Regulation 2017/745 on medical devices, a unique device identification code (UDI) is placed on the device label and packaging. 8.Equivalent technical solutions. Whenever standards, technical assessments, technical specifications and technical reference systems referred to in Art. 1 point 2 and paragraph. 3 of the Public Procurement Act, the contractor should assume that such a reference is accompanied by the words ‘or equivalent’. N.B.: If the trade name of the company, commodity or product is indicated in the tender documentation, the Ordering Party shall allow equivalent solutions in accordance with the technical data and parameters contained in the documentation. The proper name is the name under which the object designated by it occurs (or would occur) both in Poland and in other countries. By an equivalent product, the Ordering Party understands a product with technical parameters, technology, functionality, performance and quality not inferior to those specified in the SWZ. The presented solutions define the minimum level of technical parameters, technology, functionality, performance and quality. If the Contracting Authority accepts solutions equivalent to those described in the documentation annexed to the FTZ, but does not specify the minimum parameters that would confirm this equivalence, the Contractor must