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, ChipOx Nellcor-compatible SpO2 and temperature feature.
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.
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.
Videos
Adview 2 Demo
Measuring BP, Heart Rate, Temperature & Pulse Oximetry Demo