Ascom (US), a supplier of mission critical on-site wireless communications, reported that its new integration suite ClinicalConneX is powered by Ascom's Unite Professional Messaging and Alarm Application.
ClinicalConneX | Cardiomax is the first Ascom medical device cleared by the US Food and Drug Administration (FDA), Center for Devices and Radiological Health (CDRH).
Cardiomax is a component within the ClinicalConneX integration suite and provides an interface to Patient Monitoring Systems that forward alarm information to Ascom handsets or a wide variety of display devices, including pagers, mobile handsets and LED signs.
Cardiomax provides near real time alarms intended to serve as a parallel, redundant, forwarding mechanism to inform healthcare professionals of particular medical related events captured by Patient Monitoring Systems.
The display device can provide a combination of visual, audio and vibratory awareness mechanisms upon receipt of the secondary alert notification.
ClinicalConneX | Cardiomax has been designed to integrate with a variety of both standards-based and proprietary Patient Monitoring Systems.