1. The subject of the order is the delivery of disposable medical devices. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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.

4. The subject of the contract has been divided into 20 parts, 5. 12. The subject of the contract will be delivered at the expense, risk and transport of the Contractor

1. The subject of the order is the delivery of disposable medical devices - drainage kit. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - blood autotransfusion kits. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - compresses. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - surgical cotton wool. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - needles for anesthesia. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - skin stapler. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - triangular slings. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - blades compatible with shaver Formula. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - ELITE blades. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - Serfas Energy electrode. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - pressure transducer. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - disposable equipment different I. 2. The subject of the contract for individual parts of the contract has been described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - drainage kit. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - disposable equipment different II. 2. The subject of the contract for individual parts of the contract has been described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - resin immobilization dressings. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - wristbands. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - support dressings. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - tupfery. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - sterile under-plaster sleepers, bands, scarves. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.

1. The subject of the order is the delivery of disposable medical devices - dressing adhesives. 2. The subject of the contract for individual parts of the contract is described in detail in the Annex to the SWZ. 3. 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. 4. The Ordering Party requires that the generic name of the product, trade name (if the product has one), manufacturer, product sizes, series, expiry date, CE symbol and catalogue code, UDI code (if applicable, in accordance with EU Regulation 2017/745) be placed on each unit packet and collective packaging. Each sterile product must have a unit (immediate) packaging. 5. The validity period of the products may not be shorter than 12 months from the moment of delivery to the Ordering Party's headquarters. 6. The subject of the contract will be delivered at the expense, risk and transport of the Contractor.