Bids Are Invited For Acquisition Of Equipment For Hospital Use (3-Channel Portable Electrocardiograph, Tissue Expander And), To Compose The Price Recording System.

Electrocardiograph, Portable, 3 Channels, Microprocessed And Digital, Which Allows The Simultaneous Acquisition Of 12 Leads; - It Must Be Capable Of Operating In Manual And Automatic Mode. - Enable Selection In Three Sensitivity Levels; - Must Have Signal For Calibration; - Must Have At Least 3 Channels; Must Have An Integrated Printing System (Printer), For Registration On Plain Or Thermal Paper; Must Print At Least 3 Channels Of Simultaneous Ecg Data; - It Must Be Capable Of Simultaneously Acquiring Signals From All Electrodes; - Automatic And Manual Selection Of Derivations; - Must Be Capable Of Printing At At Least Speeds Of 25 And 50 Mm/Second; - Activated By Membrane Keyboard Or Easy-To-Clean Keys With Function Indicator Leds. - Must Include In The Records, At A Minimum, The Following Information:. Date And Time Of Recording; Sensitivity Adjustment; Travel Speed; Derivation Identification; Protection Against Defibrillator Discharge, Filter, Expander, Tissue, For Skin Graft, Made Of Stainless Steel Or Superior Material, Weight Less Than 5Kg Composed Of: - Replaceable Blade Shaft With Diameter Of Approximately 32Mm, 36Mm, 64Mm, 120Mm Or Shaft Of Replaceable Stainless Steel Blades With Spring Mechanism And At Minimum Two Adjustments; - 10 Skin Graft Conductors, Sterile And Disposable, Compatible With The Equipment; - Box/Container For Accommodating Accessories (Blade Shafts And Expander) For Autoclave Sterilization. Minimum 2-Year Warranty. Primary Packaging Packed In Accordance With Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Appropriate Technique; According To Rdc 185/2001; The Label Of The Primary Packaging And/Or The Product Itself Must Contain Identification Information And Characteristics Of The Product, Such As: Name Of The Manufacturer, Batch, Date Of Manufacture, Expiration Date Of The Product, Name Of The Person Responsible, Equipment, For Testing Otoacoustic Emissions (Eoa) And Brainstem Auditory Evoked Potential (Abr/Bera/Apr) In A Unique Device For Neonatal Hearing Screening With The Following Minimum Characteristics: -Perform Transient Evoked Otoacoustic Emissions (Oae) Measurements (Te) And By Product Of Distortion (Dp); - Perform Brainstem Auditory Evoked Potential Test (Abr/Bera/Apr); - Have Software(S) That Performs Transient Oae, Distortion Oae And Auditory Evoked Potential, Data Storage And Export With Their Lifetime Licenses; - Must Be Able To Perform The Requested Tests Without The Need For An External Computer; - The Equipment Must Provide Necessary Parameters For Identifying Hearing Loss Of 35 Db; -Must Store Data From At Least 200 Measurements; -Have Outputs For Computer And Printer Or Wireless Communication With These Equipment; Accessories: -1 (One) Printer Compatible With Equipment With Sufficient Inputs Par, 11/01/2024