|Introduction / Description|
Information about when the Vocera Communications EMDAN product should not be used.
This section of the Directions For Use (DFU) is intended to describe when the device should not be used (contraindications). The device should not be used under known or reasonably foreseeable hazardous conditions where the risk of use clearly outweighs any possible benefit.
Vocera Communications Engage Medical Device Alert Notification is contraindicated as a primary alarm notification system for medical devices or medical device system alarms.
Vocera's Engage Medical Device Alert Notification is contraindicated in the event of any of the following foreseeable hazards of which users should become aware: