Described are a system, method, and computer program product for tracking endoscopes in a forced-air drying cabinet including a compressor, a support arrangement, and an inner area accessible by a door. The method includes receiving a signal from a signal emitting member attached to or associated with an endoscope and determining an identifier of the endoscope. The method includes determining a drying protocol for the endoscope based on the identifier and identifying the support arrangement, associated with an airflow output, to support the endoscope. The method includes determining a connection status indicative of whether the endoscope has been connected to the airflow output. The method includes, in response to the connection status indicating the endoscope has been connected to the airflow output, initiating a drying process according to the drying protocol for the endoscope by causing the compressor to create an airflow from the airflow output through the endoscope.

Described are a system, method, and computer program product for tracking endoscopes in a forced-air drying cabinet including a compressor, a support arrangement, and an inner area accessible by a door. The method includes receiving a signal from a signal emitting member attached to or associated with an endoscope and determining an identifier of the endoscope. The method includes determining a drying protocol for the endoscope based on the identifier and identifying the support arrangement, associated with an airflow output, to support the endoscope. The method includes determining a connection status indicative of whether the endoscope has been connected to the airflow output. The method includes, in response to the connection status indicating the endoscope has been connected to the airflow output, initiating a drying process according to the drying protocol for the endoscope by causing the compressor to create an airflow from the airflow output through the endoscope.

A device for establishing and maintaining a sterile environment for conducting surgical procedures is disclosed. In particular, the tent-like device provides an interior space attachable to a patient's skin to allow surgical treatment of the patient. Several aspects of the invention are directed to devices to be used in connection with such a surgical procedure using the tent-like device. According to the invention, an isolation device for providing a sterile operation chamber above a skin region of a patient is provided, in particular for performing a surgical procedure, said isolation device comprising an inflatable bag coupled to a support frame, the support frame having a transport configuration and an operation configuration. In the transport configuration, the first inflatable bag is confined, such as to have compact dimensions. In the operation configuration, the first inflatable bag is extended, such as to form said sterile operation chamber.

A mobile cart that holds a bag for receiving solid waste generated during a medical or surgical procedure. The cart includes a sensor that monitors whether or not an object containing metal is placed in the bag. A processor monitors the signal output by the sensor. If the sensor signal indicates that an object with a minimal amount of metal is placed in the bag, the processor momentarily asserts an audible alarm and continuously asserts a light alarm. The light alarm remains asserted until turned off. If, while the light alarm is on, the sensor signal indicates a second object with the minimal amount of waste is placed in the container, the processor again momentarily asserts the audible alarm. This provides notice that it may be necessary to investigate the contents of the bag to determine if not one but two or more objects were inadvertently discarded.

A mobile cart that holds a bag for receiving solid waste generated during a medical or surgical procedure. The cart includes a sensor that monitors whether or not an object containing metal is placed in the bag. A processor monitors the signal output by the sensor. If the sensor signal indicates that an object with a minimal amount of metal is placed in the bag, the processor momentarily asserts an audible alarm and continuously asserts a light alarm. The light alarm remains asserted until turned off. If, while the light alarm is on, the sensor signal indicates a second object with the minimal amount of waste is placed in the container, the processor again momentarily asserts the audible alarm. This provides notice that it may be necessary to investigate the contents of the bag to determine if not one but two or more objects were inadvertently discarded.

A tissue cutting device has an outer sleeve with a distal window and an inner cutting sleeve which moves past the window to cut tissue. The inner cutting sleeve has a lumen which may have a larger proximal diameter than distal diameter. A perimeter of the window may comprise a dielectric material. A distal edge of the inner sleeve may be displaced inwardly.

A patient support apparatus has a movable patient couch, a support unit, and a coupling unit for coupling with a detector unit of a medical imaging apparatus, wherein the patient support apparatus has a damping unit that is designed to damp and/or compensate forces which act on the patient support apparatus coupled with the detector unit.

A thrombectomy catheter deployment for operation of a thrombectomy catheter may include a stand alone drive unit and a disposable pump/catheter assembly which is manually placed into a carriage assembly in the drive unit. The pump/catheter assembly may have a plurality of preconnected components including a tubular structure and a thrombectomy catheter connected thereto. A barcode reader may sense specific operational data pertaining to an individual pump and may provide an interface for operation of the reciprocating linear actuator.

A thrombectomy catheter deployment for operation of a thrombectomy catheter may include a stand alone drive unit and a disposable pump/catheter assembly which is manually placed into a carriage assembly in the drive unit. The pump/catheter assembly may have a plurality of preconnected components including a tubular structure and a thrombectomy catheter connected thereto. A barcode reader may sense specific operational data pertaining to an individual pump and may provide an interface for operation of the reciprocating linear actuator.

An improved fluid flow gauging device includes a light enhanced acrylic block flow tube to optimize visualization of pressure readings. An LED or other light source is fitted to the top of the flow tube and illuminates a float or bobbin from above to provide more accurate readings, especially in low light conditions such as modern operating rooms. In addition, the light enhanced flow tube provides a mechanical backup in the case of failure of newer electronic systems and visually matches the graphical flow display, simultaneously providing a double-check of the electronic system.