GTR 113368276
Tenders Are Invited For Purchase Of Medical Equipment And Apparatus For The Specialist Hospital In Zabrze Sp. Z O. O.; Case No. Dzp/07 Tp/2026.
ICB — International Competitive Bid
Closed
central europe
Tender Information
GTR Reference
113368276
Tendering Authority
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Tender No
DZP/07 TP/2026
Financer Name
Self-Funded
Work Title
Tenders Are Invited For Purchase Of Medical Equipment And Apparatus For The Specialist Hospital In Zabrze Sp. Z O. O.; Case No. Dzp/07 Tp/2026.
Bid Type
ICB — International Competitive Bid
Country
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Geographical Region
central europe
Political Region
European Union
Last Date of Bid Submission
29-05-2026
Closed
Work Detail
Package No. 1 - Video Rectoscope Set X 2 Pcs. A Detailed Description Of The Subject Of The Order Is Attached As Annex No. 3 To The Swz - Technical Parameters, Assortment And Price Form. Chapter Iii Of The Swz. 3. Conditions Required From Contractors - Contractors Submitting An Offer In The Procedure Declare That They Undertake To Comply With The Following Requirements: 1) They Will Offer Equipment Consistent With The Description Of The Subject Of The Order - Technical Parameters. 2) They Will Offer Complete Equipment, Brand New, Not Ex-Exhibition, Year Of Production Not Earlier Than 2026. 3) They Will Ensure The Transport Of The Equipment To The Ordering Partys Headquarters At Their Own Expense And Risk. After Installing The Subject Of The Order, The Contractor Will Take Away All Transport And Other Packaging Delivered And Not Required To Be Retained By The Ordering Party For The Purpose Of Possible Warranty Activities. 4) They Will Offer The Subject Of The Order That Meets The Requirements Specified In:• Act On Medical Devices Of April 7, 2022 (Journal Of Laws 2024.1620 Of 2024/11/05)• Regulation Of The Minister Of Health Of November 5, 2010 On The Method Of Classifying Medical Devices (Journal Of Laws Of 2010, No. 215, Item 1416),• Regulation Of The Minister Of Health Of February 17, 2016 On Essential Requirements And Compliance Procedures For Medical Devices (Journal Of Laws Of 2016, Item 211),• Regulation (Eu) 2019/1020 Of The European Parliament And Of The Council Of June 20, 2019 On Market Surveillance And Product Compliance - To The Extent Applicable.• Notice Of The President Polish Committee For Standardization Of August 9, 2019 On Harmonized Standards (M.P. Of 2019, Item 940), • Council Directive 93/42/Eec Of June 14, 1993 Regarding Medical Devices (Journal Of Laws Of 2019, Item 169.1, As Amended), • Regulation (Eu) 2017/745 Of The European Parliament And Of The Council Of 5 April 2017 On Medical Devices, Amending Directive 2001/83/Ec, Regulation (Ec) No. 178/2002 And Regulation (Ec) No. 1223/2009 And Repealing Council Directives 90/385/Eec And 93/42/Eec (Oj U.U.E.L.2017, Item 117.1, As Amended)5) Transport Of All Medical Devices Will Take Place In Accordance With The Requirements Specified In The Current Documents Confirming The Admission Of The Subject Of The Order To Trading And Use In Accordance With The Medical Devices Act Of April 7, 2022. Pursuant To Eu Regulation (Eu) 2017/745 (Mdr Regulation), The Distributor Of Medical Devices Is Obliged To Store And Transport In Accordance With The Conditions Specified By The Manufacturer.6) They Will Sign A Contract With Annexes, The Template Of Which Is Annex No. 4 To The Swz.7) They Will Offer A Minimum Warranty Period: Min. 24 Months For Packages 2,3,4,5 And Min. 36 Months For Package No. 1 From The Date Of Signing The Equipment Handover And Acceptance Protocol.8) The Equipment Handover And Acceptance Protocol Will Be Signed After The Equipment Has Been Accepted (Without Comments), The Con
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