Tenders Are Invited For Medical Gases - Liquid Oxygen - Okpi in Hungary

Work Detail

Medical Gases - Liquid Oxygen - Okpi. General Description: Eü-I Liquid Oxygen: Total Planned Quantity Of Eü-I Liquid Oxygen = 360,000 M3 (Basic Planned Quantity: 306,000 M3) Development Of A Signaling System (I.E. Reaching And Monitoring The Filling Level Of The Liquid Oxygen Tank On The Web Based On The Requirements Of The Technical Description): 1 Pc. With Liquid Oxygen, With Delivery Within 1 Working Day Of The Order, With The Creation Of A Filling System Under The Following Conditions. The Offered Products: • Must Be Suitable For The Purposes Specified By The Bidder; • They Must Be Suitable Without Special Stipulation For The Purposes For Which Other Products Of The Same Type Or Purpose Are Usually Used; • They Must Have The Quality That Is Usual For Products Of The Same Type Or Purpose, And Which The Bidder Can Expect, Taking Into Account The Nature Of The Products And The Public Statement Of The Bidder, The Manufacturer, Or Their Representative Regarding The Specific Properties Of The Products; • It Must Have The Qualities And Qualities Required By The Tenderer, And It Must Have The Qualities And Qualities Included In The Description Given By The Tenderer And In The Offer; • It Must Meet The Quality Requirements Laid Down In The Law. The Winning Bidder Is Obliged To Deliver All Products In Such A Way That Their Warranty (Usability) Complies With The Professional And Quality Assurance Regulations In Force At All Times. In The Absence Of This, The Bidder May Refuse To Accept The Delivered Product. Regarding The Offered Product(S), The Bidder Must Submit In His Bid, If Relevant, The 16/2012. (Ii.16.) In Order To Prove The Conformity Of The Medical Device To The Provisions Of § 9, Paragraph (2) Of The Cr., The Manufacturers Declaration Of Conformity Required By The Mdr Or The Decree On Medical Devices And - If Necessary For Placing The Medical Device On The Market On The Basis Of The Mdr Or The Decree On Medical Devices - A Ce Conformity Assessment Certificate Or Ogyéi License. The 2005 Xcv. Act And 53/2004. (Vi. 2.) Pursuant To The Eszcsm Decree, The Tenderers Activity Related To The Subject Of This Procurement Is Subject To A Permit. The Tenderer Will Conclude The Contract Only If The Successful Tenderer Has This License (Pharmaceutical Wholesale License). Tenderer 321/2015. (X. 30.) Government Regulation (Regulation) § 46, Paragraph (3) Establishes That The Reference To A Thing, Process, Activity, Person, Patent Or Trademark Of The Make, Origin, Type Specified In The Invitation To Initiate The Procedure And In The Public Procurement Documents Is Made Only For The Purpose Of Clearly Defining The Nature Of The Object, And The Name Must Be Understood As Or Equivalent. Proof Of Equivalence Is The Responsibility Of The Tenderer

Contact Information