What You'll get:
Augustine Bair Hugger 505 Patient Warming System + 90050 Rolling Cart
Attached Power Cord
Anything Else Not Mentioned or Pictured NOT INCLUDED.
Other Accessories that are Not pictured or mentioned under "What You'll Get" are Not included
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Pulled from a working environment. Unit tested to power on with no problems. All buttons and controls are functional and responsive. Works great!
Pictures are of the actual unit. Scratches and scuffs from typical use. Units buttons have been worn down but are still functional. Please reference pictures for cosmetics.
Taken from the Internet:
Dimensions: 13 in. high x 10 in. deep x 11 in. wide 33 cm high x 25 cm deep x 28 cm wide
Mounting: IV pole clamp, bedrail hook with safety strap; can be placed on hard surface
Relative Noise Level: 53 decibels
Hose: Detachable, flexible, washable; compatible with the 241 blood/fluid warming system
Filtration System: 0.2µm level
Recommended Filter Change: Every 12 months or 500 hours of use.
Temperature Control: Electronically controlled using a thermocouple sensor
Heat Generated: 1800 BTUs (average)
System time to 100°F (37.7°C): ~17 secs
Operating temperatures: Air temperatures reaching the patient are approximately 2°C lower than the listed temperatures.
Average temperatures at the end of the hose:
HIGH: 43°C ± 3°C 109.4°F ± 5.4°F
MED: 38°C ± 3°C 100.4°F ± 5.4°F
LOW: 32°C ± 3°C 89.6°F ± 5.4°F
Thermostat: Independent bulb and capillary
Overcurrent Protection: Dual fused input lines
Alarm System: Over-heat: flashing red light with audible alarm; heater shuts down
Certifications: IEC 60601-1; IEC/EN 60601-1-2; UL 60601-1; CAN/CSA-C22.2,No.601.1; EN 55011; EN 80601-2-35.
Classification: MEDICAL — GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1; CAN/CSA-C22.2, No.601.1; ANSI/AAMI ES60601-1:2005 CSA-C22.2 No. 60601-1:08; EN 80601-2-35; Control No.4HZ8
Classified under IEC 60601-1 Guidelines (and other national versions of the Guidelines) as Class I, Type BF, Ordinary equipment, Continuous operation. Not suitable for use in the presence of flammable anesthetic mixtures with air or with oxygen or nitrous oxide. Classified by Underwriters Laboratories Inc. with respect to electric shock, fire and mechanical hazards only, in accordance with UL 60601-1, EN 80601-2-35 and in accordance with Canadian/CSA C22.2, No. 601.1. Classified under the Medical Device Directive as a Class IIb device.
Blower Motor: Operating speed: 3150 rpm
Airflow: 28-30 cfm
Power Consumption: Peak: 1000W
Leakage: current <100µA
Heating Element: 850W Resistive
Power Cord: 15-foot, SJT, 3 cond., 10A 4.6 meter, HAR, 3 cond., 10A
Device ratings: 110-120 VAC, 60 Hz, 9.5 Amperes, or 220-240 VAC, 50 Hz, 4.5 Amperes, or 100 VAC, 50/60 Hz, 10 Amperes
Fuses: 10A, 200mA (110 - 120 VAC Units) 6.3A, 100mA (220 - 240 VAC Units) 15A, 160mA (100 VAC Units)
Diagnostics: Over-heat test can be performed by the biomedical group
Items are sold as-is with no returns or refunds available unless explicitly stated.