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Patient population Adult and pediatric patients (age 3 and above).
Method of measurement Oscillometric
Initial inflation pressure 160mmHg +/- 20mmHg
Blood pressure range (mmHg) 60 < Systolic BP < 270, 30 < Diastolic BP < 170
Blood pressure accuracy Measurements determined with this device are equivalent to those obtained by a trained observer using the cuff/stethoscope auscultation method, within the limits prescribed by the American National Standard, Electronic or automated sphygmomanometers.
Blood pressure determination time 35-40 seconds typical for Adult cuff
Heart rate range 30-200 bpm +/- 2% or +/- 3 bpm, whichever is greater
Temperature range 86°F (30.0°C) – 109.4°F (43.0°C)
Temperature accuracy +/- 0.2°F (+/-0.1°C)
Functional oxygen saturation range 40-100%
Functional oxygen saturation accuracy 70-100% +/- 2 digits
(Note: because pulse oximeter equipment measurements are statistically distributed, only about two-thirds of pulse oximeter equipment measurements can be expected to fall within ± 2 digits of the value measured by a CO-oximeter.)
Operating conditions 10°C (50°F) to 40°C (104°F) Less than 90% RH
Storage conditions -20°C (-4°F) to 55°C (131°F) Less than 90% RH
Power External power supply for non-battery version: Globtek model: GTM21089-1506-T3 (SunTech part number: 19-0013-00)
External power supply for Battery version, rechargeable by Globtek model: GTM21089-1509-T3 (SunTech part number 19-0014-00)
Calibration Check once per year for BP and Temperature
Safety systems Independent hardware over-pressure circuit and redundant software overpressure algorithm to limit cuff pressure to less than 330 mmHg. Independent hardware timing circuit and redundant software timer algorithm to limit the duration of a blood pressure cycle to less than 180 seconds.
Dimensions Length = 5.5 inches, Height = 11.5 inches, Width = 3.8 inches; Length =14.0 cm, Height = 29.2 cm, Width = 9.7 cm
Standards UL60601-1, CAN/CSA C22.2 601-1
IEC 60601-1, IEC 60601-1-2 (EMC), IEC 60601-1-4, ISO 9919, AAMI SP10:2002, ASTM E 1112, EN 12470-3
Meets “Non-invasive Sphygmomanometers — General Requirements & Supplementary Requirements for Electro-Mechanical BP Measuring Systems”, EN 1060-1, EN 1060-3
Classification Protection against electric shock: Class II (for non-battery version), Internally Powered Equipment (for battery version); Applied parts: Type BF; Mode of operation: Continuous

 

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