Zad. 1 – Mikroskop laboratoryjny dla Zakładu Bakteriologii

TENDER DESCRIPTION

3.3. The Contracting Authority’s requirements regarding the subject matter of the contract: 1) the offered medical device must have approvals, certificates and be registered in accordance with legal provisions requiring approvals, certificates and registration, 2) the offered medical device must be placed on the market and put into use in accordance with the requirements of the Act of 7 April 2022 on medical devices (Journal of Laws 2024, item 1620), 3) the offered medical device must comply with standards or technical specifications applicable to this device; In the event that the offered medical device does not require notification to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, the Contractor is obliged, at its own expense and within its own scope, to carry out all actions necessary to satisfy all legal requirements related to the placing on the market and use of the device on the territory of the Republic of Poland. The Contractor shall carry out such actions within the time limits resulting from the applicable regulations and provide the Contracting Authority, within those time limits, with the relevant documents…

TENDER BRIEF

TENDER DOCUMENTS