The subject of the contract is the purchase and delivery of magnetic resonance imaging equipment along with necessary modernization work as part of the National Reconstruction and Resilience Plan – component D "Effectiveness, accessibility and quality of the health protection system", investment D1.1.1 Development and modernization of the infrastructure of high-specialty care centers and other medical entities. The detailed description of the subject of the order includes:
- Summary of required conditions and parameters;
- Description of construction works along with attachments;
- Draft provisions of the contract for public procurement along with attachments, which constitute annexes to this specification (available in separate files).

LOT-0002
Purchase and delivery of magnetic resonance imaging equipment along with necessary modernization work.
1. The subject of the order is the purchase and delivery of magnetic resonance imaging equipment along with necessary modernization work as part of the National Reconstruction and Resilience Plan – component D "Effectiveness, accessibility and quality of the health protection system", investment D1.1.1 Development and modernization of the infrastructure of high-specialty care centers and other medical entities. The detailed description of the subject of the order includes: Summary of required conditions and parameters; Description of construction works along with attachments, Draft provisions of the contract for public procurement along with attachments, which constitute annexes to this specification (available in separate files).
2. Conditions for participation in the proceedings:
1. Ability to operate in the economic trade.
The Ordering Party does not specify conditions in this regard.
2. Authorization to conduct specific economic or professional activities, if arising from separate regulations.
The Ordering Party does not specify conditions in this regard.
3. Economic or financial situation.
The Ordering Party does not specify conditions in this regard.
4. Technical or professional capacity.
The Ordering Party does not specify conditions in this regard.
A list of substantive evidence required to confirm compliance with the conditions for participation in the proceedings, which the Contractor submits at the request of the Ordering Party (applies to the Contractor whose offer has been rated highest):
1. Ability to operate in the economic trade.
The Ordering Party does not require any substantive evidence.
2. Authorization to conduct specific economic or professional activities, if arising from separate regulations.
The Ordering Party does not require any substantive evidence.
3. Economic or financial situation.
The Ordering Party does not require any substantive evidence.
4. Technical or professional capacity.
The Ordering Party does not require any substantive evidence.
3. Information on the substantive evidence.
In order to confirm the compliance of the offered supplies with the requirements and characteristics specified in the summary of the required conditions and parameters, the Contractor must submit the following documents along with the offer:
- completed summary of required conditions and parameters by indicating the full name of the device, manufacturer’s name, country of origin, distributor, and year of production along with filling out the "Offered Parameter" column,
- a declaration of compliance for medical devices in accordance with the Act of April 7, 2022, on medical devices (Journal of Laws 2024, item 1620) – included in the Offer Form,
- for goods that are medical devices a certificate of conformity issued by a notifying body or a declaration of conformity;
- for medical devices offered within the subject of the order, the Contractor must submit one of the following documents:
- in the case of manufacturers or authorized representatives residing or based within the territory of Poland – products notification to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products;
- in the case of distributors and importers employed or based in Poland, who have introduced products intended for use within this territory – notification of this introduction to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products;
- a document confirming registration in the Medical Devices Register, notification to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, or notification to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products;
- documents such as: catalog cards, brochures, data sheets, technical specifications, manufacturer’s declarations, reports, instructions, etc. containing the description of the subject of the order along with catalog numbers if available, confirming compliance with the requirements specified in the summary of required conditions and parameters which serves as Annex 4 to the Terms of Reference.
- declaration of conformity with the CE standard;
If the contractor has not submitted the substantive evidence or if the submitted substantive evidence is incomplete, the Ordering Party will call for their submission or supplementation on the basis of Article 107(2) of the Public Procurement Law within the deadline set by themselves.
NOTE!!!
The Ordering Party does not provide for the supplementation of substantive evidence that serves to confirm compliance with the requirements specified in the description of the evaluation criteria.