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Neonatal Heated Crib. The Neonatal Heated Crib Must Be Designed For Intensive Care In Newborns, With Microprocessor Digital Temperature Control, Offering Operation Modes Such As Pre-Heating, Manual And Servo Controlled. The Heating System Must Use Infrared Radiation, With A Centralized Polished Stainless Steel Reflector And Resistance Protective Rail, May Include A Rotating Or Rotational Heater With A Minimum Angle Of 180°. Neonatal Phototherapy Must Be Integrated, Composed Of At Minimum 15 Blue Leds And 4 White Leds, With Adjustable Intensity Control From 0% To 100% At 10% Intervals, And A Light Emitting Source With A Minimum Lifespan Of 50,000 Hours. Electrical Power Must Be Equal To Or Greater Than 65 W, With A Light Focus Of At Least 50 Cm And A Minimum Area Of 225 X 380 Mm. The Equipment Must Operate With Automatic Frequency Selection (50/60 Hz), Have A Line Filter And Have A Low Noise Level. The Bed Must Be Radio-Transparent, With Flaps, Hospital Retractable Column. The Hospital Retractable Column Must Be Manufactured In A High-Resistance Metal Structure, Which May Be Made Of Phosphated Carbon Steel, Steel Sheet With Epoxy Painting Or A Combination Of Aluminum And Steel With Electrostatic Powder Painting. The Equipment Must Have A Vertical Lifting System With A Minimum Travel Of 400 Mm, Driven By A Pneumatic Piston, Mechanical Key Or Remote Control. It Must Contain Outlets For Medicinal Gases (Oxygen, Compressed Air And Vacuum), With Connections Compatible With Standards Abnt Nbr 11906, Nbr 12188 And/Or Nbr 13534. The Column Must Include Five Hospital Standard Electrical Sockets, Distributed On A Strip With Protection Against Surges Or Overloads, In Addition To A Technical Grounding System With A Pin. Security. The Equipment Must Have A Serum Support, Supply Pressure Indicator Gauges And A Modular Front Panel, With The Possibility Of Customization And Installation Of Alarms Or Additional Indicators. The Dimensions And Finish Must Be, Conventional Defibrillator. The Conventional Defibrillator Must Be Multifunctional, With Manual And Semi-Automatic (Aed) Operating Modes, In Addition To Cardiac Stimulation And Continuous Monitoring Functions. It Must Use Biphasic Technology, Such As Truncated Exponential Or Bte, With Adjustable Energy Delivery Capacity Between 1 And 360 Joules, Performing Automatic Compensation Of Thoracic Impedance In Real Time To Guarantee Effective Defibrillation. The Equipment Must Allow Rapid Activation, With An Initialization Time Of Less Than 3 Seconds And Charging Of 200 J In Up To 3 Seconds. The Interface Must Be Intuitive, With A Color Lcd Display Of At Least 4.3, And May Include Touchscreen Operation And Simultaneous Visualization Of The Ecg Tracing And Heart Rate. It Must Offer Visual And Audible Guidance During The Service, With A Simplified Three-Step Interface (Select Power, Charge, Apply Shock). The Equipment Must Be Compatible With Wi-Fi Connectivity (2.4G/5G), Automatic External Defibrillator (Aed). The Automatic External Defibrillator (Aed) Must Be Portable, Lightweight And Microprocessed, Developed For Emergency Care In Cases Of Cardiorespiratory Arrest In Adult And Pediatric Patients. It Must Use Biphasic Wave Technology, Such As Truncated Exponential, Scope™, Star™ Or Equivalent, With Adjustment. Automatic Waveform And Energy According To Patient Impedance In Compliance With International Resuscitation Guidelines
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