Equipment for the control of biomedical devices during extracorporeal circulation. The equipment includes at least one basic structure and a (e.g., tangible) controller or a control unit/device/component/etc. that is assembled on the basic structure and provided with at least one control unit/etc. operationally connectable to at least one biomedical device for extracorporeal circulation and configured to control it. The controller/etc. comprise at least one emergency control unit, operationally connectable to the biomedical device and configured to control the latter following a malfunction of the control unit.

A fluid supply warning and communication system including a digital regulator in fluid tight engagement with a primary fluid reservoir. A method of using the fluid supply warning and communication system by flowing a fluid from a primary fluid reservoir to an end use appliance and detecting flow rate and pressure of the fluid with a digital regulator. A gas supply warning and communication system including an oxygen flow monitor that monitors SpO2, flow rate, pulse rate, and battery levels. A method of using the gas supply warning and communication system by flowing oxygen from a primary gas reservoir to an end use appliance, and measuring SpO2, flow rate, pulse rate, tank status, and battery levels.

A method of initiating operation of an external unit for a medical system further comprising an internal unit implanted into a body of a patient; a transformer core arranged under the skin of the patient; and internal cabling connecting the internal unit and the transformer core, the internal cabling comprising an internal winding around the transformer core, wherein the external unit comprises external cabling including an external winding around the transformer core to allow supply of power from the external unit to the internal unit via the transformer core, the method comprising the steps of: evaluating, by the external unit, a signal indicative of a magnetic flux in the transformer core; when the signal indicates that the magnetic flux in the transformer core is below a predefined threshold flux, providing power to the internal unit by the external unit via the transformer core.

A clamping device for acting onto a medical tubing includes a clamp arrangeable on the medical tubing and displaceable between an open position in which the clamp unblocks the medical tubing and a close position in which the clamp closes the medical tubing. The clamping device further includes a drive system configured to act on the clamp for switching the clamp between the open position and the close position. The clamping device also includes a main control circuit and a secondary control circuit electronically independent from the main control circuit, and a relay switchable between a first position and a second position. In the first position, the relay electronically couples the drive system to the main control circuit while the drive system is electronically decoupled from the secondary control circuit. In the second position, the relay electronically couples the drive system to the secondary control circuit while the drive system is electronically decoupled from the main control circuit. The secondary control circuit causes the clamp to adopt the close position when the relay is in the second position.

A liquid ventilation system includes a reservoir holding a perfluorochemical (“PFC”) fluid, and a suction pump connected to the reservoir to reduce pressure within the reservoir. A sensor is configured to measure an intra-lung pressure. An appliance is configured to be disposed within a patient. The appliance carries an injector to supply the PFC fluid through the appliance. An extraction valve is disposed on an extraction line between the appliance and the reservoir. The extraction valve is arrangeable between a first position enabling fluid communication from the appliance to the reservoir and a second position disabling fluid communication from the appliance to the reservoir.

A syringe pump includes a lead screw, a motor, and a sliding block assembly. The lead screw has threads and the motor is coupled to the lead screw to rotate it. The half-nut housing has a half nut and a barrel cam. The half nut is disposed within the half-nut housing. The half nut has half-nut threads at an end adjacent to the lead screw void. The half nut engages or disengages with the threads of the lead screw. The half nut includes a half-nut cam-follower surface and a half nut slot. The barrel cam is disposed within the half-nut housing and engages with the half-nut cam-follower surface. The barrel cam includes a pin to fit within the half nut slot such that the barrel cam rotates between a first position and a second position to actuate the half nut between the engagement position and the disengagement position, respectively.

Disclosed herein is a system and method for controlling oxygen supply equipments. The system is equipped with pressure sensors coupled to the oxygen supply equipments. Depending on the oxygen supply selected by a user for the patient, the pressure sensor monitors the current pressure of the preset oxygen supply during an inhalation phase corresponding to the patient. If the current pressure is less than a minima value or if a pressure drop rate is higher than or equal to a threshold rate or both, the system generates an alarm notifying the user to check the preset oxygen supply and in the meanwhile switches the preset oxygen supply from one oxygen supply equipment to another oxygen supply equipment or vice-versa.

A method includes receiving, from a primary pressure sensor, a pressure measurement indicative of a pressure of a patient cavity and controlling, by an insufflator, a supply of the insufflation fluid to the patient cavity based on the pressure measurement from the primary pressure sensor. The method further includes delivering, by a trocar, the supplied insufflation fluid to the patient cavity via an access port, wherein: the access port comprises a seal and a retractor; and the access port facilitates access therethrough to the patient cavity.

Systems and methods for nitric oxide generation are provided. In an embodiment, an NO generation system can include a controller and disposable cartridge that can provide nitric oxide to two different treatments simultaneously. The disposable cartridge has multiple purposes including preparing incoming gases for exposure to the NO generation process, scrubbing exhaust gases for unwanted materials, characterizing the patient inspiratory flow, and removing moisture from sample gases collected. Plasma generation can be done within the cartridge or within the controller. The system has the capability of calibrating NO and NO.sub.2 gas analysis sensors without the use of a calibration gas.

Provided is an extended use self-contained, wearable medical device. The device is preferably configured with an infusion deployment mechanism for variably inserting and retracting an infusion needle to different depths, or completely retracting the infusion needle from the infusion site and then re-inserting the infusion needle after a predetermined period of time, throughout an infusion cycle for extending the viability of the infusion site. Another embodiment comprises dual needle deployment mechanisms which may also variably insert and retract the infusion needles. A flow sensor is preferably provided for detecting the stoppage of flow through the infusion cannula and signaling the needle deployment mechanism to attempt infusion at a different depth or to deploy a second infusion needle. A re-fillable reservoir assembly is preferably provided for supplying a drug over the extended use of the device. Another embodiment comprises a partially reusable and partially disposable medical device implementing the above features.