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 and heart rate feature only. 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) Oral/Axillary Probe and Well (Blue) (20) Probe Covers (1) User Manual
Technical Specifications Dimensions Height: 8" Width: 6.75" Depth: 5.2" 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). Temperature Temperature Accuracy Quick Mode (Oral): ± 0.3°C Std. Mode (Aux/Rectal): ± 0.1°C Direct Mode: ± 0.1°C Response Time 4 Sec (Quick Mode) 10-15 Sec. (Axillary/Rectal) 60 Sec. (Direct Mode) 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