MAQUET has received FDA 510(k) clearance for an upgrade of the SERVO-i ventilator for conditional use in the magnetic resonance (MR) environment. The SERVO-i is intended for treatment and monitoring of all patients, neonatal, pediatric and adult who require mechanical ventilation. The new SERVO-i MR environment option is capable of providing critically ill patients with advanced ventilatory care using the same machine wherever they are in the hospital—in the ICU, in the MR examination room and during transport to and from the MR room.
||MR Press Release
||Critical Care News Article "New Opportunities for MRI examinations of ventilated ICU patients’s