Tenders Are Invited For Emergency Training Dolls – Purchase And Delivery Of A High-Fidelity Phantom For The Air Ambulance Service

Emergency Training Dolls – Purchase And Delivery Of A High-Fidelity Phantom For The Air Ambulance Service. 1. The Subject Of The Order Is The Delivery Of A Brand New, Unused, High-Fidelity Phantom Free From Physical And Legal Defects, Together With Transport, Unloading, Carrying, Assembly (If Applicable) And Commissioning, Demonstrating The Correct Operation Of All Functions Of The Subject Of The Order, As Well As Conducting Instruction/Training For The Indicated Staff Of The Ordering Party At The Headquarters At Ul. Moonowa 5 In Warsaw. The Kit Must Enable Practical Training, Providing High-Fidelity Training That Reproduces The Anatomy And Physiology Of An Adult Human, With The Ability To Treat Injuries, Perform A Wide Range Of Critical Life-Saving Procedures And Advanced Resuscitation Procedures, As Well As Learning How To Cooperate And Control The Situation By The Medical Team In Conditions Corresponding To Real Clinical Scenarios. 2. A Detailed Description Of The Subject Of The Order Is Included In Annex No. 1 To The Swz (Description Of The Subject Of The Order). The Conditions For The Implementation Of The Subject Of The Order Are Included In The Draft Provisions Of The Agreement Constituting Annex No. 2 To The Swz. 3. The Ordering Party Does Not Allow The Submission Of Offers For Medical Devices From Third Countries That Are Not Parties To International Agreements. 4. Third Countries That Are Not Parties To International Agreements Are Countries Other Than Those Indicated In Art. 16B Of The Act On Public Procurement, Countries Are Deemed To Be Not Parties To The Agreement Of The World Trade Organization On Government Procurement Or Other International Agreements To Which The European Union Is A Party, Guaranteeing Access To The Public Procurement Market On The Basis Of Reciprocity And Equality. 5. For The Country Of Origin Of The Medical Device, In Accordance With Art. 60 Of Regulation (Eu) No 952/2013 Of The European Parliament And Of The Council Of 9/10/2013 Establishing The Union Customs Code, The Country Is Deemed To Be The Country In Which: 1) The Medical Device Was Completely Manufactured, 2) The Medical Device Was Subjected To The Last Significant, Economically Justified Processing Or Processing, In An Enterprise Adapted For This Purpose, Which Resulted In The Production Of A New Product Or Constituted An Important Stage Of Production, If More Than One Person Was Involved In The Production Of The Medical Device Than One Country.