1. The subject of the contract is the supply of medical equipment and apparatus. 2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ. 3. The subject of the order also includes the assembly and commissioning of the offered equipment and training of the Ordering Party's staff in its current operation, maintenance and operation (does not apply to parts no. 3 - 8). 4. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, European Union Directive 93/42/EEC of 14 June

1993 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. It must have Declarations of Conformity and CE Certificates.

1. The subject of the order is the supply of medical equipment and apparatus - laser therapy apparatus.

2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ.

3. The subject of the contract also includes the assembly and commissioning of the offered equipment and the training of the Ordering Party's staff in its ongoing operation, maintenance and operation.

4. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

5. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, the European Union Directive 93/42/EEC of 14 June 1993 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. It must have Declarations of Conformity and CE Certificates.

1. The subject of the contract is the supply of medical equipment and apparatus - peripheral nerve stimulator

2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ.

3. The subject of the contract also includes the assembly and commissioning of the offered equipment and the training of the Ordering Party's staff in its ongoing operation, maintenance and operation.

4. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

5. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, the European Union Directive 93/42/EEC of 14 June 1993 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. It must have Declarations of Conformity and CE Certificates.

1. The subject of the contract is the supply of medical equipment and apparatus - transport refrigeration equipment

2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ.

3. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

4. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, the European Union Directive 93/42/EEC of 14 June 1993 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. It must have Declarations of Conformity and CE Certificates.

1. The subject of the contract is the supply of medical equipment and apparatus - gel positioners

2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ.

3. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

4. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, the European Union Directive 93/42/EEC of 14 June 1993 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. It must have Declarations of Conformity and CE Certificates.

1. The subject of the contract is the supply of medical equipment and apparatus - temperature recorder

2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ.

3. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

4. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, the European Union Directive 93/42/EEC of 14 June 1993 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. It must have Declarations of Conformity and CE Certificates.

1. The subject of the contract is the supply of medical equipment and apparatus - anti-decubitus devices

2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ.

3. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

4. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, the European Union Directive 93/42/EEC of 14 June 1993 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. It must have Declarations of Conformity and CE Certificates.

1. The subject of the contract is the supply of medical equipment and apparatus - a specialized trolley for the transport of surgical instruments

2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ.

3. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

4. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, the European Union Directive 93/42/EEC of 14 June 1993 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. It must have Declarations of Conformity and CE Certificates.

1. The subject of the contract is the supply of medical equipment and apparatus - Trolley for patients over 150 kg

2. The subject of the contract for individual parts of the contract is described in detail in Appendix No. 2 to the SWZ.

3. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

4. The offered subject of the order must be compliant and approved for marketing and use in the territory of the Republic of Poland in accordance with the requirements of the Act of 7 April 2022 on medical devices, the European Union Directive 93/42/EEC of 14 June 1993 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. It must have Declarations of Conformity and CE Certificates.