Frequently asked questions
Yes. The charger can be connected directly to the operating table and charges the battery during operation.
Yes. Patient positioning can be adjusted quickly and precisely during surgery using either the hand control or optional foot control. The backrest, seat, leg section, and headrest can be adjusted smoothly, while the table can be tilted forward and backward to optimize surgical access, patient comfort, and surgeon ergonomics. This flexibility helps improve workflow efficiency and reduce physical strain on clinical staff.
Under normal use, a fully charged lithium battery supports approximately 50 procedures. The actual number of procedures depends on factors such as average patient weight and how frequently the table’s motors are operated during each procedure. The estimate of 50 operating cycles is based on an average patient weight of 80 kg (176 lbs) and normal motor usage. The hand control features a battery status indicator and provides an audible warning when the remaining battery capacity is low.
Yes. RiEye Mk2S has been developed to provide excellent ergonomic access for the surgeon, particularly around the patient’s head. The table also offers generous legroom underneath, allowing comfortable use of microscope pedals and other equipment commonly used in microsurgical procedures.
The battery can be charged in an external charging dock or directly on the operating table.
Yes. The hand control features large, intuitive buttons with clear symbols and indicator lights that display the selected function and ongoing movements.
The battery can be removed and reinstalled without tools using a simple one-handed release mechanism.
Yes. A clearly marked red button ("Trend") on the hand control activates the Trendelenburg position. The position can be customized during installation in collaboration with hospital staff to meet local clinical preferences. This function can be useful if a patient experiences dizziness or signs of fainting.
Yes. RiEye Mk2S is classified as a medical device under MDR (EU) 2017/745, complies with relevant international safety and performance requirements, and is FDA registered and manufactured in compliance with applicable medical device regulations.
Yes. Up to six user-defined positions can be stored and recalled.
