Request For Information Regarding The Counterpulsator in Finland

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This Is Not A Procurement Notice Or A Request For Tender, But The Purpose Of This Request For Information Is To Map The Suppliers Available On The Market Who Have In Their Selection An Antipulsator With Consumables Related To The Device, The Maintenance And Support After The Warranty Period That Is Part Of The Device. The Aim Of This Request For Information Is To Map And Collect Information On What Kind Of Alternatives There Are In The Market For The Antipulsator (Iabp). The Device Must Be Suitable For The Treatment Of Adult Patients And The Device Has A Transport Certificate For The Transfer Of Patients Outside The Hospital. The Device Must Operate On Batteries For At Least Two (2) Hours. The Device Must Have Modern Rhythm Detection Based On Both The Ecg And The Pressure Curve. The Device Must Be Automatic/Semi-Automatic. The Device Must Also Have A Connection For A Fiber Optic Catheter. The Device And Consumable Parts/Device-Related Accessories Suitable For The Device Are Ce-Marked And Mdr Approved (Or Mdr Approval Is Being Prepared). Device Support And Training Must Be Found In Finland. This Request For Information Does Not Ask For Or Give Offers For This. The Publication Of This Notice Does Not Obligate The Procurement Entity To Carry Out The Actual Procurement. With This Request For Information, Only Information Is Requested About Counterpulsators On The Market With Their Accessories And In Terms Of Maintenance And Support Related To The Device. The Information Collected With This Request For Information Will Remain Completely Confidential And Will Only Be Used For Planning A Possible Acquisition. Those Who Responded To The Request For Information Will Not Be Compensated For Answering The Request For Information. This Is A Market Survey In Accordance With Section 65 Of The Procurement Act.

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