ADC, a world leader in core diagnostic products for more than 30 years, has partnered with SunTech Medical®, the premier developer of innovative blood pressure technology, to create the next generation in modular diagnostics: The ADC ADView 2 Modular Diagnostic Station. Features and Benefits Clinical-grade Advantage™ BP technology from SunTech Medical Contemporary, compact design with an integrated handle and easy-to-read display Manual blood pressure mode for real-time verification Next-generation EMR ready with HL7 messaging for electronic data transfer Network enabled with built-in Ethernet or optional Wi-Fi Lithium-ion power for longer-lasting battery life and a lighter weight Built-in memory with up to 99 charting sessions New Pediatric Mode to ensure accurate measurements for younger patients Firmware upgradeable This Adview 2 model comes with blood pressure, heart rate and ChipOx Nellcor-compatible SpO2 feature. Optional thermal printer can be connected to your ADView 2 using one of the unit’s two USB ports. 1 paper roll is included with the optional printer. Optional barcode scanner available
Materials Included Adview 2 Monitor Unit (1) Lithium Ion Battery (1) Adult Plus Cuff (1) Large Adult Plus Cuff (1) Mini USB to USB Cable (1) Adult SpO2 Finger Sensor (1) 8' Extension Cable (1) User Manual
Technical Specifications Dimensions Height: 8" Width: 6.75" Depth: 5.2" SpO2 Saturation Normal (No Motion): 70-100%Arms ± 2% Saturation Motion: N/A Low Perfusion: N/A Pulse Heart Rate: 20-300 BPM: ±3 BPM Pulse Heart Rate w/ Motion: 20-300 BPM: ±3 BPM Blood Pressure/Heart Rate Range Pressure: Diastolic: 20-200 mmHg (adult), 20-160 mmHg (pediatric). Systolic: 40-260 mmHg (adult), 40-230 mmHg (pediatric) Heart Rate: 30-220 BPM (Beats Per Minute) Accuracy: Meets or exceeds ANSI/AAMI/ISO 81060-2:2013 standard for non-invasive accuracy (±5mmHg mean error with 8mmHg standard deviation). Conditions For Use Operating: 10°C (50°F) to 40°C (104°F) 15 – 90% RH non-condensing - 700 kPa - 1060 kPa. Operating the monitor in an environment at maximum temperature can produce temperatures exceeding 41°C (41.6°C highest recorded) on a patient-applied part. Storage -20°C (-4°F) to 55°C (149°F) 15 – 90% RH non-condensing - 500 kPa - 1060 kPa. Performance can be affected if used or stored outside the specified temperature, humidity, or altitude listed in the ranges above. Power: Internal Power Supply Input: 100-240 VAC @ 1.5A max, 50-60 Hz. Output: +9VDC @ 5A IEC 320 type input connector. Calibration The accuracy of cuff -pressure transducers/indicators should be verified bi-annually. Safety Systems Independent hardware over-pressure circuit and redundant software overpressure algorithm to limit cuff pressure to less than 300 mmHg (+20/-10mmHg). Independent hardware timing circuit and redundant software timer algorithm to limit the duration of a blood pressure cycle to less than 180 seconds. Standards ANSI/AAMI ES60601-1:2005/(R)2012 and A1:2012, C1:2009/(R)2012 and A2:2010/(R)2012, EN 60601-1:2006/A1:2013, IEC 60601-1-2: 2007 EMC, IEC 80601-2-30: 2013, ISO 80601-2-61: 2011, ISO 15223-1:2012, ISO 10993-1, 2009, ISO 10993-5, 2009, EN ISO 10993-10, 2010, ISO 81060-2:2013, EN 50419: 2006, EN ISO 14971:2009, CSA C22.2 No. 60601-1, EN ISO 81060-1: 2012, IEC 60601-1-6: 2013 Classifications Equipment Classification: Class IIa per MDD, Class I (Electrical Shock), Continuous mode of operation, CE Ingress of Liquid Ingress Protection: IPX1: This device is protected against harmful effects of dripping water per IEC 60529.
Warranty Information 3-Year Warranty on the Unit 2-Year Warranty on the Blood Pressure Cuffs 1-Year Warranty on the Battery