Tenders Are Invited For Medical Equipments – Provision Of Role Capability Dbr

Medical Equipments – Provision Of Role Capability Dbr. Creation Of A Dynamic Procurement System, The Subject Of Which Is: Procurement Of Specialist Materials, Tools And Services To Ensure The Health And Other Functioning Of Role Level Care Units, Up To A Net Amount Of Huf 45,960,046,803 Within A Period Of 48 Months. During The Implementation Of The Dbr, The Tenderer Is The Kbt. Based On Section 107 (2), The Exact Technical Description And Contractual Conditions For The Specific Public Procurements To Be Implemented In The System Will Be Made Available To Bidders Participating In The Dbr At The Same Time As The Invitation To Tender Is Sent. Product Categories And Planned Quantities: Medical Specialist Materials 1,317,825 Pieces Medical Equipment 3,931 Pieces Medical Furniture 2,788 Pieces Medical Containers, Tent Kits 8 Sets Tools And Services That Ensure And Support The Operation Of Role Levels 107,000 Pieces The Highest Contract Value To Be Concluded In The Dynamic Purchasing System Per Product Category: I. Net 3,341 Huf 637,000 Ii. Net Huf 1,102,568,844 Iii. Net Huf 79,555,059 Iv. Net Huf 1,208,945,926 V. Net Huf 4,225,000,000 Bidder Kbt. On The Basis Of § 107, Paragraph (2), It Reserves The Possibility That During The Implementation Of The Dbr, At The Same Time As The Invitation To Tender Is Sent, The Options For Partial Tendering May Be Determined In The Invitation To Tender, Depending On The Subject Matter And Nature Of The Specific Public Procurements, For The Specific Procurement Requirement Contained Therein. (Guidelines Of The Council Operating Within The Framework Of The Public Procurement Authority On The Dynamic Procurement System (February 10, 2022) All Applicants Who Meet The Eligibility Criteria Will Be Admitted To The Dbr, The Number Of Applicants To Be Invited To Tender Will Not Be Limited. Regarding The Definition Of The Technical Description, The Tenderer Draws Attention To The Provisions Of § 9 Of Government Decree 16/2012 (Ii.16): The Bidder Shall Demonstrate The Conformity Of The Medical Device In Accordance With The Provisions Of The Mdr, The Ivdr, The Decree On Medical Devices, Or The Decree On In Vitro Diagnostic Medical Devices With A Declaration Of Conformity And - If The Placing Of The Medical Device Or The In Vitro Diagnostic Medical Device On The Market Is Necessary On The Basis Of The Mdr, The Ivdr, The Decree On Medical Devices, Or The Decree On In Vitro Diagnostic Medical Devices - Ce Conformity Must Prove With A Certificate.