Supply of sterile and non-sterile medical products for patients of the Specialist Hospital in Zabrze Sp. z o. o.; Case No. DZP/14 PN/2026.

The Specialist Hospital in Zabrze Sp. z o. o. in Poland from Europe region has released this tender for Supply of sterile and non-sterile medical products for patients of the Specialist Hospital in Zabrze Sp. z o. o.; Case No. DZP/14 PN/2026. The subject of the order has been divided into 26 Lots, i.e.: • Part 1 Package No. 1 Equipment: Transfusion devices, catheters, tubes, drains, connectors, disposable procedural, gas and specialist equipment, injections • Part 2 Package No. 2 Hemostatic pressure dressing after blood collection • Part 3 Package No. 3 Specialist dressings • Part 4 Package No. 4 Disposable procedural equipment, specialist dressings • Part 5 Package No. 5 Specialist dressings, gauze and non-woven dressing sets, sterile metal instruments • Part 6 Package No. 6 Equipment: Transfusion devices, catheters, tubes, drains, connectors, disposable procedural, gas and specialist equipment, injections, hemostats, simple and specialist dressings • Part 7 Package No. 7 Biopsy containers with formalin • Part 8 Package No. 8 Matrix Hemostatic • Part 9 Package No. 9 Tests for the diagnosis of contact dermatitis • Part 10 Package No. 10 Bacterial-viral respiratory filter • Part 11 Package No. 11 Tracheostomy tubes • Part 12 Package No. 12 Dressing for central venous catheters with chlorhexidine • Part 13 Package No. 13 Transfusion devices, cannulas, needles, caps for intravenous catheters, syringes, oxygen masks • Part No. 14 Package No. I Containers for used needles and disposable instruments • Part No. 15 Package No. II Containers for histopathological specimens • Part No. 16 Package No. III Medical blood pressure monitors • Part No. 17 Package No. IV Accessories for ECG/USG examinations - Electrodes and gels • Part No. 18 Package No. V Small medical equipment - tourniquet, thermometers • Part No. 19 Package No. VI Disposable secretion inserts for medical suction devices • Part No. 20 Package No. VII Defibrillation electrodes • Part No. 21 Package No. VIII Defibrillation electrodes • Part No. 22 Package No. IX Neutral electrodes, VIO 300D and APC2 coagulation accessories • Part No. 23 Package No. X Stimulation electrodes • Part No. 24 Package No. XI Ducts and bedpans • Part No. 25 Package No. XII Spirometry accessories • Part No. 26 Package No. XIII Disposable inserts for the suction system with gelling powder, inactivating secretions A detailed description of the subject of the order is attached as Appendix No. 3 to SWZ – Assortment and price form. 1. For packages 1-7 (except for package 1 items 6, 21, 73, package 5 items 216 and 217, package 6 item 278) and packages 10-13 and packages II-XIII, the Ordering Party requires that the offered medical devices meet the requirements of the Act of 7 April 2022 on medical devices (Journal of Laws 2024, item 1620, i.e. of 2024.11.05, as amended), the Regulation of the Minister of Health of 5 November 2010 on the method of classifying medical devices (Journal of Laws of 2010, No. 215, item 1416), the Regulation of the Minister of Health of 17 February 2016 on the essential requirements and compliance procedures for medical devices (Journal of Laws of 2016, item 211),Regulation (EU) 2019/1020 of the European Parliament and of the Council of 20 June 2019 on market surveillance and compliance of products - to the extent applicable and in accordance with Directive 93/42/EEC (Journal of Laws 1993, item 169.1, as amended) and had certificates authorizing use on the medical market in force in Poland and in the EU, Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 (MDR). 2. For packages 1-7 (except for package 1 items 6, 21, 73, package 5 items 216 and 217, package 6 item 278) and packages 10-13, the Ordering Party requires that medical devices have a UDI code carrier on the label and on all higher levels of the packaging in the case of class III implantable devices and class IIa and IIb devices – if it applies to the selected medical device. 3. For packages 8-9, the Ordering Party requires medicinal products that meet the requirements specified in the Act of 6 September 2001 - Pharmaceutical Law (Journal of Laws 2026, item 612, i.e. of 2026.05.07), consistent with the description of the subject of the order contained in the Assortment and Pricing Forms constituting Appendix No. 3 to the Technical Specifications. 4. For package 1 items 21, 73, for package 5 items 216 and 217 The Ordering Party requires cosmetics within the meaning of the Act of 4 October 2018 on cosmetic products (consolidated text: Journal of Laws of 2018, item 2227). 5. In package 6, item 278, the Ordering Party requires a biocidal product subject to the Act of 9 October 2015 on biocidal products (Journal of Laws of 2021, item 24, i.e. of 2021.01.05, as amended). 6. The Ordering Party informs that if the description gives trade names of products, indicates trademarks, patents or the origin, source or specific process that characterizes the product supplied by a specific Contractor, they refer only to the quality, type of product, and the Ordering Party cannot, for objective reasons, describe the subject of the order in a sufficiently precise and understandable manner, therefore such indication is accompanied by the words "type" "or equivalent". 7. In each case of using in the description of the subject of the order the characteristics of the material, product referred to in Art. Pursuant to Article 101, Section 1, Item 2 of the Public Procurement Law, the Contracting Authority allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet to meet the requirements set by the Contracting Authority. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications (TSQ), by submitting a list of equivalent goods (materials). In such a case, the Contractor is obligated to demonstrate, in particular through the relevant evidence, that the goods (materials) it offers meet the requirements (equivalence criteria) specified by the Contracting Authority.on market surveillance and compliance of products – to the extent applicable and in accordance with Directive 93/42/EEC (Journal of Laws 1993, item 169.1, as amended) and have certificates authorizing use on the medical market in force in Poland and in the EU, Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 (MDR). 2. For packages 1-7 (except for package 1 items 6, 21, 73, package 5 items 216 and 217, package 6 item 278) and packages 10-13, the Ordering Party requires that medical devices have the UDI code carrier on the label and on all higher levels of the packaging in the case of class III implantable devices and class IIa and IIb devices – if this applies to the selected medical device. 3. For packages 8-9, the Ordering Party requires medicinal products that meet the requirements specified in the Act of 6 September 2001 - Pharmaceutical Law (Journal of Laws 2026, item 612, i.e. of 2026.05.07), consistent with the description of the subject of the order contained in the Assortment and Pricing Forms constituting Appendix No. 3 to the Technical Specifications. 4. For package 1, items 21, 73, for package 5, items 216 and 217, the Ordering Party requires cosmetics within the meaning of the Act of 4 October 2018 on cosmetic products (i.e. Journal of Laws of 2018, item 2227). 5. In package 6, item 278, the Ordering Party requires a biocidal product subject to the Act of 9 October 2015 on biocidal products (Journal of Laws 2021, item 24, i.e. of 2021.01.05, as amended). 6. The Ordering Party hereby informs that if the description includes product trademarks, trademarks, patents, or the origin, source, or specific process that characterizes a product supplied by a specific Contractor, these refer only to the quality or type of the product, and the Ordering Party cannot, for objective reasons, describe the subject of the order in a sufficiently precise and understandable manner, therefore such indication is accompanied by the words "type" or "or equivalent." 7. In each case of using material or product characteristics referred to in Art. 101, paragraph 1, item 2 of the Public Procurement Law in the description of the subject of the order, the Ordering Party allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet to meet the requirements set by the Ordering Party. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications by submitting a list of equivalent goods (materials). In such a case, the Contractor is obliged to demonstrate, in particular by means of the evidence in question, that the goods (materials) offered by him meet the requirements specified by the Ordering Party (equivalence criteria).on market surveillance and compliance of products – to the extent applicable and in accordance with Directive 93/42/EEC (Journal of Laws 1993, item 169.1, as amended) and have certificates authorizing use on the medical market in force in Poland and in the EU, Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 (MDR). 2. For packages 1-7 (except for package 1 items 6, 21, 73, package 5 items 216 and 217, package 6 item 278) and packages 10-13, the Ordering Party requires that medical devices have the UDI code carrier on the label and on all higher levels of the packaging in the case of class III implantable devices and class IIa and IIb devices – if this applies to the selected medical device. 3. For packages 8-9, the Ordering Party requires medicinal products that meet the requirements specified in the Act of 6 September 2001 - Pharmaceutical Law (Journal of Laws 2026, item 612, i.e. of 2026.05.07), consistent with the description of the subject of the order contained in the Assortment and Pricing Forms constituting Appendix No. 3 to the Technical Specifications. 4. For package 1, items 21, 73, for package 5, items 216 and 217, the Ordering Party requires cosmetics within the meaning of the Act of 4 October 2018 on cosmetic products (i.e. Journal of Laws of 2018, item 2227). 5. In package 6, item 278, the Ordering Party requires a biocidal product subject to the Act of 9 October 2015 on biocidal products (Journal of Laws 2021, item 24, i.e. of 2021.01.05, as amended). 6. The Ordering Party hereby informs that if the description includes product trademarks, trademarks, patents, or the origin, source, or specific process that characterizes a product supplied by a specific Contractor, these refer only to the quality or type of the product, and the Ordering Party cannot, for objective reasons, describe the subject of the order in a sufficiently precise and understandable manner, therefore such indication is accompanied by the words "type" or "or equivalent." 7. In each case of using material or product characteristics referred to in Art. 101, paragraph 1, item 2 of the Public Procurement Law in the description of the subject of the order, the Ordering Party allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet to meet the requirements set by the Ordering Party. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications by submitting a list of equivalent goods (materials). In such a case, the Contractor is obliged to demonstrate, in particular by means of the evidence in question, that the goods (materials) offered by him meet the requirements specified by the Ordering Party (equivalence criteria).Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 (MDR). 2. For packages 1-7 (except for package 1 items 6, 21, 73, package 5 items 216 and 217, package 6 item 278) and packages 10-13, the Ordering Party requires that medical devices have the UDI code carrier on the label and on all higher levels of the packaging in the case of class III implantable devices and class IIa and IIb devices - if it applies to the selected medical device. 3. For packages 8-9, the Ordering Party requires medicinal products that meet the requirements specified in the Act of 6 September 2001 - Pharmaceutical Law (Journal of Laws 2026, item 612, i.e. of 2026.05.07), consistent with the description of the subject of the order contained in the Assortment and Pricing Forms constituting Appendix No. 3 to the SWZ. 4. For package 1, items 21, 73, for package 5, items 216 and 217, the Ordering Party requires cosmetics within the meaning of the Act of 4 October 2018 on cosmetic products (consolidated text: Journal of Laws of 2018, item 2227). 5. In package 6, item 278, the Ordering Party requires a biocidal product subject to the Act of 9 October 2015 on biocidal products (Journal of Laws of 2021, item 24, i.e. of 2021.01.05, as amended). 6. The Ordering Party informs that if the description gives trade names of products, indicates trademarks, patents or the origin, source or specific process that characterizes the product supplied by a specific Contractor, they refer only to the quality and type of product, and the Ordering Party cannot, for objective reasons, describe the subject of the order in a sufficiently precise and understandable manner, therefore such indication is accompanied by the words "type" "or equivalent". 7. Whenever the description of the subject of the contract uses material or product characteristics referred to in Article 101, Section 1, Item 2 of the Public Procurement Law, the Ordering Party allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet to meet the requirements set by the Ordering Party. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications by submitting a list of equivalent goods (materials). In such a case, the Contractor is obligated to demonstrate, in particular through the relevant evidence, that the goods (materials) offered meet the requirements specified by the Ordering Party (equivalence criteria).Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 (MDR). 2. For packages 1-7 (except for package 1 items 6, 21, 73, package 5 items 216 and 217, package 6 item 278) and packages 10-13, the Ordering Party requires that medical devices have the UDI code carrier on the label and on all higher levels of the packaging in the case of class III implantable devices and class IIa and IIb devices - if it applies to the selected medical device. 3. For packages 8-9, the Ordering Party requires medicinal products that meet the requirements specified in the Act of 6 September 2001 - Pharmaceutical Law (Journal of Laws 2026, item 612, i.e. of 2026.05.07), consistent with the description of the subject of the order contained in the Assortment and Pricing Forms constituting Appendix No. 3 to the SWZ. 4. For package 1, items 21, 73, for package 5, items 216 and 217, the Ordering Party requires cosmetics within the meaning of the Act of 4 October 2018 on cosmetic products (consolidated text: Journal of Laws of 2018, item 2227). 5. In package 6, item 278, the Ordering Party requires a biocidal product subject to the Act of 9 October 2015 on biocidal products (Journal of Laws of 2021, item 24, i.e. of 2021.01.05, as amended). 6. The Ordering Party informs that if the description gives trade names of products, indicates trademarks, patents or the origin, source or specific process that characterizes the product supplied by a specific Contractor, they refer only to the quality and type of product, and the Ordering Party cannot, for objective reasons, describe the subject of the order in a sufficiently precise and understandable manner, therefore such indication is accompanied by the words "type" "or equivalent". 7. Whenever the description of the subject of the contract uses material or product characteristics referred to in Article 101, Section 1, Item 2 of the Public Procurement Law, the Ordering Party allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet to meet the requirements set by the Ordering Party. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications by submitting a list of equivalent goods (materials). In such a case, the Contractor is obligated to demonstrate, in particular through the relevant evidence, that the goods (materials) offered meet the requirements specified by the Ordering Party (equivalence criteria).which meet the requirements specified in the Act of 6 September 2001 - Pharmaceutical Law (Journal of Laws 2026, item 612, i.e. of 2026.05.07), consistent with the description of the subject of the order contained in the Assortment and Pricing Forms constituting Appendix No. 3 to the Technical Specifications. 4. For package 1, items 21, 73, for package 5, items 216 and 217, the Ordering Party requires cosmetics within the meaning of the Act of 4 October 2018 on cosmetic products (i.e. Journal of Laws of 2018, item 2227). 5. In package 6, item 278, the Ordering Party requires a biocidal product subject to the Act of 9 October 2015 on biocidal products (Journal of Laws of 2021, item 24, i.e. of 2021.01.05, as amended). 6. The Ordering Party hereby informs that if the description includes product trademarks, trademarks, patents, or the origin, source, or specific process that characterizes a product supplied by a specific Contractor, these refer only to the quality or type of the product, and the Ordering Party cannot, for objective reasons, describe the subject of the order in a sufficiently precise and understandable manner, therefore such indication is accompanied by the words "type" or "or equivalent." 7. In each case of using material or product characteristics referred to in Art. 101, paragraph 1, item 2 of the Public Procurement Law in the description of the subject of the order, the Ordering Party allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet to meet the requirements set by the Ordering Party. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications by submitting a list of equivalent goods (materials). In such a case, the Contractor is obliged to demonstrate, in particular by means of the evidence in question, that the goods (materials) offered by him meet the requirements specified by the Ordering Party (equivalence criteria).which meet the requirements specified in the Act of 6 September 2001 - Pharmaceutical Law (Journal of Laws 2026, item 612, i.e. of 2026.05.07), consistent with the description of the subject of the order contained in the Assortment and Pricing Forms constituting Appendix No. 3 to the Technical Specifications. 4. For package 1, items 21, 73, for package 5, items 216 and 217, the Ordering Party requires cosmetics within the meaning of the Act of 4 October 2018 on cosmetic products (i.e. Journal of Laws of 2018, item 2227). 5. In package 6, item 278, the Ordering Party requires a biocidal product subject to the Act of 9 October 2015 on biocidal products (Journal of Laws of 2021, item 24, i.e. of 2021.01.05, as amended). 6. The Ordering Party hereby informs that if the description includes product trademarks, trademarks, patents, or the origin, source, or specific process that characterizes a product supplied by a specific Contractor, these refer only to the quality or type of the product, and the Ordering Party cannot, for objective reasons, describe the subject of the order in a sufficiently precise and understandable manner, therefore such indication is accompanied by the words "type" or "or equivalent." 7. In each case of using material or product characteristics referred to in Art. 101, paragraph 1, item 2 of the Public Procurement Law in the description of the subject of the order, the Ordering Party allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet to meet the requirements set by the Ordering Party. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications by submitting a list of equivalent goods (materials). In such a case, the Contractor is obliged to demonstrate, in particular by means of the evidence in question, that the goods (materials) offered by him meet the requirements specified by the Ordering Party (equivalence criteria).Therefore, such an indication is accompanied by the words "type" or "or equivalent." 7. Whenever the characteristics of a material or product referred to in Art. 101, paragraph 1, item 2 of the Public Procurement Law are used in the description of the subject of the contract, the Ordering Party allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet in order to meet the requirements set by the Ordering Party. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications by submitting a list of equivalent goods (materials). In such a case, the Contractor is obligated to demonstrate, in particular using the relevant evidence, that the goods (materials) offered meet the requirements specified by the Ordering Party (equivalence criteria).Therefore, such an indication is accompanied by the words "type" or "or equivalent." 7. Whenever the characteristics of a material or product referred to in Art. 101, paragraph 1, item 2 of the Public Procurement Law are used in the description of the subject of the contract, the Ordering Party allows the submission of offers containing equivalent goods (materials). All goods (materials) specified in the documentation, originating from specific manufacturers, define the minimum quality parameters and performance characteristics that the goods must meet in order to meet the requirements set by the Ordering Party. The Contractor may refer in its offer to the use of goods (materials) equivalent to those described in the Technical Specifications by submitting a list of equivalent goods (materials). In such a case, the Contractor is obligated to demonstrate, in particular using the relevant evidence, that the goods (materials) offered meet the requirements specified by the Ordering Party (equivalence criteria). with tender notice no. 686506-2026 published on 07 Oct 2026. The tender is due to expire on 10 Nov 2026. This tender is sourced from TED Europa and is eligible for suppliers interested in Medical consumables. Interested bidders can obtain further information including complete bid documents or ways to participate by registering on Tender Impulse and referencing via Tender Impulse ID 15305281.