Drager Fabius MRI anesthesia machine received FDA clearence





Draeger Medical, Inc. announced Dräger Fabius MRI receives FDA clearance to provide advanced anesthesia technology in the MR environment.  The Fabius MRI is designed for use with 1.5T and 3.0T MRI systems. An integrated Teslameter provides an acoustic alarm if the Fabius MRI is positioned within a field strength greater than 40mTesla (400 Gauss).

The Fabius MRI employs the same user interface as Dräger’s Fabius GS, Fabius Tiro and Apollo machines, creating a uniform and consistent interface for the anesthesia provider wherever anesthesia is required. The size of the MRI system often requires the anesthesia provider to be outside the room or some distance away from the device during an examination. To accommodate this, additional optical alarm displays (LEDs) at the top of the system provide visual indication for all alarm conditions for the safety of the patient in this
specialized environment.

The Fabius MRI also continues the same quality of care to which clinical personnel are accustomed – from the OR application to the MRI environment. The standard configuration includes the advanced ventilation modes (volume and pressure controlled, pressure support and SIMV) that are especially needed for the care of premature infants, newborns, and ICU patients and makes them available for use in this environment.

The high-speed piston ventilator provides controlled compliance compensation, even with the longer ventilation tubes often used in the MRI environment, providing even for the smallest infant.  Dräger also offers a range of MRI-compatible accessories, all tested and certified for use with the Fabius MRI machine.