Abstract: A flow tube (10) has a housing (12, 14) including at least a first housing half (12) and a second housing half (14). Each housing half (12, 14) has a connection surface (20, 22) intended for combination with the other housing half (12, 14). The connection surfaces (20, 22) enclose a mounting gap (30) for an orifice element (16). Outside of the mounting gap (30) the connection surfaces (20, 22) butt against each other in some sections by respective abutting surface portions (32, 34), and outside of the mounting gap (30) and outside of the abutting surface portions (32, 34) the housing halves (12, 14) are integrally combined with each other. A method is provided for producing the flow tube, namely for integrally joining the housing halves (12, 14).

Abstract: Pump assemblies for fluid flow are provided. A pump assembly includes a fluid flow pump, a first tubing pathway configured to receive a fluid input tube and a second tubing pathway configured to receive a fluid output tube. A non-contact tubing dimension measurement assembly is configured to measure a tubing outside diameter (OD). Methods of operating a fluid flow pump are also provided.

Abstract: A surgical system for the treatment of ocular problems including a surgical cassette, a surgical console operatively coupled to the surgical cassette and further including a processor, a vacuum source positioned in-line with a vacuum regulator and a mass air flow controller, and a tank fluidly connected to the mass air flow controller, wherein the processor is configured to calculate an air flow set point in accordance with a received at least one user-defined fluid flow rate set point; and wherein the mass air flow controller modulates air flow from the tank to the vacuum source in accordance with the received the air flow set point to meet a user-defined fluid flow rate.

Abstract: The present invention provides a system for managing occlusions during phacoemulsification surgery. More specifically, the present invention provides a user of a surgical console an alert when a partial or full occlusion of a surgical tool causes the vacuum pressure to become greater than a predetermined pressure threshold setting and automatically reduces the vacuum pressure when the predetermined pressure threshold setting is exceeded.

Abstract: A system and method for promoting and safeguarding the wellbeing of patients in relation to a fluid injection may obtain patient data; determine, based on the patient data, an initial risk prediction for a patient for a fluid injection to be administered to the patient, the initial risk prediction including a probability that the patient experiences at least one adverse event in response to the fluid injection; provide, to a user device, before the fluid injection is administered to the patient, the initial risk prediction; determine, after the fluid injection is started, sensor data associated with the patient; determine, based on the sensor data determined after the fluid injection is started, a current risk prediction including a probability that the patient experiences the at least one adverse event in response to the fluid injection; and provide, to the user device, the current risk prediction.

Abstract: Sensors are disclosed that detect whether a cannula is properly inserted to its full depth in a subject's skin. The sensors may be used with a blood glucose monitor, or with a continuous insulin infusion pump, infusion set, or other system involving intermittent or continuous testing and/or drug delivery.

Abstract: An apparatus (1) for negative pressure wound therapy comprises a source of reduced pressure (10) and first (22a) and second (26a) chambers, the first chamber being in fluid communication with the source of reduced pressure such that a negative pressure may be generated in the first chamber, the negative pressure being prevented from exceeding a predetermined value by way of a pressure release means (30), and the second chamber comprising means (28) for establishing a fluid connection with a wound. A valve (24) between the first and second chambers permits the negative pressure in the second chamber to increase in response to an increase in the negative pressure in the first chamber and prevents the negative pressure in the second chamber from dropping in response to a drop in the negative pressure in the first chamber.

Abstract: A biopsy device includes an instrument set and an instrument drive unit removably coupled to the instrument set. The instrument set includes an instrument set housing; an elongate outer cannula having a tissue receiving aperture in a side wall thereof; an elongate inner cannula disposed within an outer cannula lumen; an aspiration vent fluidly coupling the outer cannula lumen to atmosphere; and an aspirate valve in the aspiration vent, and configured such that the outer cannula lumen is vented to atmosphere only when the aspirate valve is open. The instrument drive unit includes a drive unit support structure removably coupled to the instrument set housing; a motorized inner cannula driver configured to axially oscillate the inner cannula relative to the outer cannula to sever tissue extending through the tissue receiving opening; and an actuating member configured to selectively mechanically prevent the aspirate valve from closing.

Abstract: An apparatus for delivering a powdered agent into a subject's body may include a first passage for receiving a pressurized gas. The apparatus also may include a container housing a powdered agent. The container may be in fluid connection with the first passage. At least a portion of the pressurized gas is introduced into the powdered agent in the container to fluidize the powdered agent. The apparatus also may include a second passage for receiving the powdered agent from the container. In a first configuration of the apparatus, the second passage may not be in fluid connection with the container. In a second configuration of the apparatus, the second passage may be in fluid connection with the container. The apparatus may be configured to transition between the first configuration and the second configuration.

Abstract: The various embodiments disclosed here relate to systems, methods, and devices for monitoring bladder health via pressure. Certain implementations are directed to patients who require daily catheterization. The various embodiments have at least one tube coupled to a catheter, a pressure sensor and a processor. Further implementations feature an optional pump and measure volume. Certain embodiments include a digital device with a software application capable of displaying the monitored readings.

Abstract: A compensating of the sensor module occurs with the implementing of the transfer function in the measuring circuit of the sensor module. The transfer function generates sensor measured values as a function of primary signal. In a later sensor calibration, sensor measured values provided on the sensor module interface are registered as a function of supplied pressure values and stored in a calibration database. In a later electronics module calibration, measured value signals provided on the signaling interface are registered as a function of sensor measured values supplied by means of a calibration signal source and stored in a calibration database, wherein the supplied sensor measured values correspond to the sensor measured values of the sensor calibration. Finally, there follows the calibration protocol creation, in which the measured value signals ascertained in the electronics module calibration are associated with the pressure values supplied in the sensor calibration.

Abstract: A system for monitoring a volume of a bladder during a surgical procedure. The system includes one or more processors; and a memory that is communicatively coupled to the one or more processors and stores one or more sequences of instructions, which when executed by one or more processors causes steps to be performed comprising: receiving information of a maximum volume of the bladder before the surgical procedure; receiving one or more ultrasound images from an ultrasonic scanner; based on the one or more ultrasound images, determining a volume of the bladder; comparing a maximum volume of the bladder to the determined volume of the bladder; and responsive to a difference between the maximum volume and determine volume of the bladder exceeding a threshold, issuing a warning associated with the difference.

Abstract: A low medicament sensor for a medicament delivery device having a reservoir, a pump, and a fluid path therebetween for medicament, the sensor including a switch and a snap dome. The snap dome is initially in contact with the switch, in fluid communication with the fluid path, and configured to snap out of contact with the switch when a pressure within the snap dome decreases below a predetermined pressure.

Abstract: A fluid management system includes a pump connectable to a fluid source. An inflow line removably connects to a cannula for delivering a fluid flow from the pump into a surgical site, such as a joint cavity. A flow pressure sensor is coupled to measure flow pressure in the inflow line and produce a measured pressure value, A controller is connected to the pump and the flow pressure sensor, and the controller maintains a pressure set point by controlling a pump speed based on a backpressure-adjusted pressure value calculated by subtracting a backpressure value selected from a backpressure table from the measured pressure value. The BAPV is monitored to determine whether the BAPV deviates outside an initial BAPV range, and corrective measure are taken should such deviations occur.

Abstract: In one aspect the present disclosure refers to a measuring arrangement for measuring of a volume change of a liquid medium located inside a liquid reservoir, the measuring arrangement comprising: a gas tight enclosure having an interior volume containing a gas reservoir and containing the liquid reservoir, wherein the liquid reservoir is filled with a liquid medium, a gas inlet in flow connection with the gas reservoir and extending through a boundary of the gas tight enclosure to an exterior of the gas tight enclosure, an outlet connectable with the liquid reservoir and extending through the boundary of the gas tight enclosure, wherein the gas reservoir and the liquid reservoir are hermetically separated by an impenetrable separation wall, and a flow meter arranged in or across the gas inlet to measure an ingress of a gaseous medium through the inlet in response to a withdrawal of the liquid medium from the liquid reservoir through the outlet.

Abstract: A manually actuated drug-injecting device is configured such that the grip strength of the entire hand (i.e., majority of fingers closing toward the palm or heel of the hand) is employed to discharge medication through a hypodermic needle and into a patient's body. The device is well suited for delivering medications with high viscosity and/or by patients (e.g., elderly patients) with reduced finger strength and dexterity. The device includes a grip member, a push member (which causes the medication to be injected), and a force-transfer mechanism that couples the grip member to the push member. Suitably, the device is configured to be held transverse to the palm of the medication-administering hand, with a discharge port located by the outer, blade edge of the administering hand, when the device is being gripped to administer medication.

Abstract: A surgical system includes an electrosurgical tool configured to be releasably coupled to a surgical robotic system having a control system. The tool has a shaft having an end effector with treatment electrodes configured to apply electrosurgical power to a tissue, and aspiration and irrigation tubes having ports in the vicinity of the electrodes. The control system can control a flow rate of an irrigation fluid based on deviation of power delivered by the electrodes to the tissue from a power set point, or based on an aspiration rate that is controlled based on tissue impedance. The tool can have first and second ports and a conduit configured to selectively provide or aspirate fluids through at least one of the ports. At least one of a flow rate and an aspiration rate are controlled by the control system based on a rotational angle of the shaft relative to a ground.

Abstract: A urinary bladder irrigation device includes: a first pipe, a second pipe, a third pipe, a liquid supply member, a liquid collection member, a detection member, and an elevation member. The first pipe has a first opening at one end thereof. The second pipe has a second opening at one end thereof. The third pipe has an end connected to another end of the first pipe and another end of the second pipe and has a third opening at another end thereof. The liquid supply member is connected to the first opening. The liquid collection member is connected to the second opening. The detection member is positioned in the second pipe. The elevation member accommodates the detection member.

Abstract: A levelling device for positioning of a medical device in relation to a patient is disclosed. The levelling device comprises a tube having fluid communication between a first end and a second end, wherein the first end is configured for connection to the medical device and the second end is configured for connection to the patient. The levelling device comprises a control unit connected to a sensor, wherein the sensor is configured to transmit sensor data to the control unit which is indicative of a pressure difference between the first and second end of the tube, and an actuator connected to the control unit, wherein the actuator is configured to connect to the medical device and to arrange a position of the medical device in relation to the patient in dependence on said pressure difference.

Abstract: Methods and systems for automatically pulsing different aspiration levels to an ocular probe are disclosed. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level, and applied to the probe in a pulsed manner.

Abstract: A flow control apparatus and method for accurate detection of occlusion conditions in a feeding set. A sensor is arranged with respect to a pumping device to produce a signal indicative of pressure in the feeding set. A control circuit that may receive the sensor signal from the sensor indicative of the pressure in the feeding set may also control operation of the pumping device. The control circuit is configured to operate the pumping device in an operational state, and in a reset state subsequent to the operational state in which the pumping device does not produce a pumping action and the pumping device is moved to a position in which the pumping device does not block the feeding set to permit fluid flow in a backflow direction opposite to the patient direction thereby relieving any built up pressure in the feeding set downstream of the pumping device.

Abstract: An injection cannula includes a hand-held mechanical motorized device to improve delivery of fat and facilitate dispersion at a recipient site. The injection cannula may, for example be a cannula for injecting fat in a cosmetic surgical procedure for fat transplantation such as percutaneous injection or injection directly into the subcutaneous fat. An electric motor, pneumatic motor, or other mechanism may be used to provide vibration.

Abstract: Methods and apparatuses for automatically switching different aspiration levels to an ocular probe are disclosed herein. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level. Control feed back of the pumps may be varied according to set thresholds.

Abstract: A fluid management system includes a disposable cassette carrying inflow and outflow tubing sections that are configured for releasably mating with a console including a control unit and a pair of roller pump heads. The console may automatically identify the disposable cassette and weigh the fluid in an inflow source. During operation, the system can monitor pressure in the working space, and provide for inflow and outflow control to maintain any desired operating parameters.

Abstract: A needle knife device and system for cutting soft tissue under skin of a patient are provided. The needle knife can include an elongated needle including a lumen and a beveled point configured to allow the elongated needle to be inserted transcutaneously into the skin of the patient. The needle knife can also include a blade that is capable of being oscillated within the lumen of the elongated needle between a retracted position where the blade is disposed within the needle and a deployed position where the blade is disposed outside the needle beyond the beveled point. A motor unit can be operatively arranged with the blade and configured to oscillate the blade.

Abstract: In some embodiments, a vitrectomy probe may include an inner cutting tube reciprocating in an outer tube. The outer tube includes a side port and the inner tube includes a distal cutting port, and, in some embodiments, an additional side port. In some embodiments, the inner tube may also include a flat upper edge that cuts across the outer tube side port. In some embodiments, a diaphragm drives the inner tube and may have an open-stroke side with a lower hardness material than a closed-stroke side. In some embodiments, an aspiration tube coupled to the vitrectomy probe may include a first aspiration tubing and a second aspiration tubing with a lower hardness than the first aspiration tubing. In some embodiments, the vitrectomy probe may be coupled to pneumatic tubing that is stepped or tapered.

Abstract: An exemplary biopsy system includes a biopsy device having a probe. The probe includes a distally extending needle and a cutter movable relative to the needle. The probe also includes a tissue sample holder detachably coupled to the proximal end of the probe. The biopsy system has a cycle where the biopsy system provides vacuum to the biopsy device, retracts the cutter to a proximal position, advances the cutter to a distal position, and transports a sample to the tissue sample holder. The biopsy system is capable of adjusting the duration of its cycle during operation of the biopsy device.

Abstract: Disclosed is a fully detachable trocar, comprising: a cannula; a support connected to one end of the cannula; a channel passing through the cannula and the support along an axial direction; an air-inflated structure arranged on the support and communicated with the channel; an air valve for controlling the air-inflated structure to turn on and off; a primary sealing component for sealing when a device is used; and a second sealing component for sealing when no device is used; the primary sealing component, the second sealing component and the support are connected in a sealing manner from top to bottom in sequence, and the primary sealing component can be independently separated from the second sealing component which can be independently separated from the support, so as to provide multiple methods for taking out tissues.

Abstract: This disclosure relates to a tissue separation system to separate the posterior vitreous cortex from the inner limiting membrane in the eye, and to the separation of other body tissues. A system includes a flexible elongate member having a proximal end and a distal end. The flexible elongate member is coupled to a fluid reservoir and has a lumen configured to deliver fluid from the reservoir for use in a surgical procedure and further includes a pump system coupled to the proximal end of the flexible elongate member and to the fluid reservoir, configured to pressurize the fluid to a pressure suitable for separating tissues. The system also includes a control system arranged to control the pump system to provide a series of pulses of fluid through the flexible elongate member and out from the distal end thereof to suitably separate the tissues during the surgical procedure.

Abstract: Methods and apparatuses for automatically switching different aspiration levels to an ocular probe are disclosed herein. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level. Control feed back of the pumps may be varied according to set thresholds.

Abstract: Systems and methods for delivering a drug or other therapy over an extended period of time (e.g., several hours, days, weeks, months, years, and so forth) are disclosed herein, as are systems and methods for monitoring various parameters associated with the treatment of a patient. Systems and methods are also disclosed herein that generally involve CED devices with various features for reducing or preventing backflow.

Abstract: A method of dispensing fluid includes three processes. A first one of these processes includes pumping fluid into a resilient variable-volume dispensing chamber. The dispensing chamber is in series with a normally present finite fluid impedance and an output. The impedance is sufficient so as to cause expansion of the dispensing chamber as it receives pumped fluid even while some fluid flows through the output. Another one of these processes includes repeatedly measuring a parameter related to volume of the dispensing chamber over time. A third one of these processes includes controlling the pumping of fluid based on repeated measurements of the parameter to produce a desired fluid flow through the output. A corresponding system for dispensing fluid implements these processes.

Abstract: Embodiments of the invention include a medicament device configured to provide stepwise instructions for using the device to a user in a particular sequence is provided. The device includes a reusable housing configured to receive a container, the reusable housing including a control interface, the control interface including at least one responsive member reactive to a user input, an actuation member configured to interact with the container, a signal output component associated with the reusable housing; and circuitry associated with the reusable housing configured to control a provision of the stepwise instructions to the user in the particular sequence.

Abstract: According to one embodiment, a method includes positioning a portion of a trocar into a patient cavity. The trocar includes an inner tubular member and an outer tubular member disposed about the inner tubular member. The outer tubular member has at least a first chamber and a second chamber separated from the first chamber. The method also includes inserting a surgical instrument into the inner tubular member, and supplying an insufflation gas to the patient cavity by providing the insufflation gas through the first chamber of the outer tubular member.

Abstract: Air drained from a patient's body can be measured after a surgical operation or trauma. The volume of air drained from the body can be determined from the weight of a vessel that has receive effluent drained the body and the volume of air that has escaped from the vessel. The effluent can include any one or a combination of air and liquid.

Abstract: The aim of the present invention is a method of sampling all or part of a sample (11) of biological matter (7), which is crude, enriched or cultured through contact with a culture medium (8), such as agar, for example in a Petri dish, using a probe (3) equipped with a terminal end (4), said sampling method comprising the steps of cooling the terminal end (4) of the probe (3), sticking all or part of the sample (11) of biological matter (7) to be sampled through contact, or by applying a pressure exerted by the terminal end (4) onto the sample (11) of biological matter (7), and sampling of all or part of the sample (11) of biological matter (7) so as to separate the sample (11) of biological matter (7) from the culture medium (8), a method of depositing into a container (9) or onto an analysis plate (14) all or part of a sample (11) of biological matter (7) stuck onto a frosted terminal end (4) of a probe, said depositing method including a step of separating the terminal end (4) of the probe (3) from all or p

Abstract: An anesthetic administration device comprising an infusion device, which is in fluid connection with a regional anesthetic needle by means of a feed tube. The infusion device comprises one or more anesthetic flow devices capable of triggering forward flow, and optionally backward flow, of the local anesthetic through the regional anesthetic needle. Forward, and optionally backward flow, of the local anesthetic through the regional anesthetic needle is controlled by a controller that comprises one or more actuator switches. The one or more actuator switches are positioned on the device such that they may be operated by hand.

Abstract: The NEEDLE KNIFE APPARATUSES, METHODS AND SYSTEMS (“NK”) may have a cannula, through which a needle knife may be deployed. The needle knife may oscillate to cut through a patient's tissue, such as muscle tissue in the forehead of a patient to eliminate forehead wrinkles. In certain embodiments, the knife portion of the needle knife is normally sheathed within a cannula during insertion into and removal from a patient. The oscillation may be performed manually or by a motor, which may be attached via a connection mechanism. The connection mechanism may include a colley system or be glued in place. Once inserted into a patient, the oscillating motor mechanism is engaged to rapidly oscillate the needle knife to expose the knife to rapidly cut soft tissue.

Abstract: An in-joint pump and control device comprising a pump and an in-joint sensor. The pump is configured to convey fluid to a body joint surgical site. The pump has an algorithm associated therewith to make calculations and to assist in controlling the operation of the pump. The in-joint sensor is operatively associated with the pump by at least a communication member. The in-joint sensor comprises a sheath, an integration member attached to the sheath, a pressure sensor connected to the integration member, and a temperature sensor adjacent the sheath. The pressure sensor is adapted to provide pressure information to the pump via the communication member. The temperature sensor is also adapted to provide temperature information to the pump via the communication member.

Abstract: A medical drainage tube for treating wounds with negative pressure includes a suction tube, a suction connector, and a ventilation sleeve. The suction tube includes a suction lumen, and a ventilation lumen including a lumen outer wall and an opening. The ventilation sleeve is arranged at the opening to surround the suction tube. The ventilation sleeve includes a sleeve wall including a sleeve inner wall arranged towards the suction tube, an annular groove arranged in the sleeve inner wall, a filter compartment arranged in the sleeve wall, a bacterial filter arranged in the filter compartment, and an air inlet arranged in the filter compartment. The annular groove communicates with the opening. The bacterial filter communicates with the annular groove. The air inlet connects the bacterial filter with the atmosphere. A part of the ventilation lumen between the annular groove and a proximal end of the suction tube is sealed off.

Abstract: The illustrative embodiments described herein are directed to a system and method for administering reduced pressure at a tissue site. The apparatus includes a reduced pressure source. The reduced pressure source generates a reduced pressure. The apparatus includes a tube having a plurality of lumens. The plurality of lumens includes at least one collection lumen. The reduced pressure source applies the reduced pressure to the tissue site through the plurality of lumens such that the at least one collection lumen receives fluid from the tissue site. The at least one collection lumen stores the fluid received from the tissue site.

Abstract: A biopsy device includes an instrument set and an instrument drive unit removably coupled to the instrument set. The instrument set includes an instrument set housing; an elongate outer cannula having a tissue receiving aperture in a side wall thereof; an elongate inner cannula disposed within an outer cannula lumen; an aspiration vent fluidly coupling the outer cannula lumen to atmosphere; and an aspirate valve in the aspiration vent, and configured such that the outer cannula lumen is vented to atmosphere only when the aspirate valve is open. The instrument drive unit includes a drive unit support structure removably coupled to the instrument set housing; a motorized inner cannula driver configured to axially oscillate the inner cannula relative to the outer cannula to sever tissue extending through the tissue receiving opening; and an actuating member configured to selectively mechanically prevent the aspirate valve from closing.

Abstract: A flow control apparatus adapted to receive a feeding set includes a housing capable of receiving at least a portion of the feeding set. A pumping device is supported by the housing and positioned to contact the feeding set when the feeding set is received by the housing so the pumping device acts on the feeding set to produce fluid flow in the feeding set for delivery of fluid to a subject. An ultrasonic sensor is supported by the housing and arranged with respect to the pumping device to produce a sensor signal indicative of a viscosity of the fluid delivered through the feeding set. A control circuit is in communication with the ultrasonic sensor for receiving the sensor signal from the sensor indicative of the viscosity of the fluid and in communication with the pumping device to control operation thereof.

Abstract: Devices and methods for guidewire assisted placement of catheters into blood vessels are described. Some of the devices and methods relate to automated or partially automated or assisted insertion and placement of an intravenous catheter into a vein or artery of a patient. Other of the devices are blood draw devices and methods for insertion and placement of an intravenous device into a vein or artery of a patient or to withdraw a blood sample from the patient. The devices also provide for guide wire tip inspection after use.

Abstract: The aim of the present invention is a method of sampling all or part of a sample (11) of biological matter (7), which is crude, enriched or cultured through contact with a culture medium (8), such as agar, for example in a Petri dish, using a probe (3) equipped with a terminal end (4), said sampling method comprising the steps of cooling the terminal end (4) of the probe (3), sticking all or part of the sample (11) of biological matter (7) to be sampled through contact, or by applying a pressure exerted by the terminal end (4) onto the sample (11) of biological matter (7), and sampling of all or part of the sample (11) of biological matter (7) so as to separate the sample (11) of biological matter (7) from the culture medium (8), a method of depositing into a container (9) or onto an analysis plate (14) all or part of a sample (11) of biological matter (7) stuck onto a frosted terminal end (4) of a probe, said depositing method including a step of separating the terminal end (4) of the probe (3) from all or p

Abstract: A multi-container transfer and deliver device and methods of mixing and transferring, the device configured to allow multiple containers to transfer and mix their respective materials and for receiving of the mixed materials to a fluid delivery device. The transfer device comprises a plurality of flow conduits for fluid flow between the multiple containers and the fluid delivery device. A drug mixing kit and optional packaging comprising a multi-container housing with a plurality of flow conduits and a plurality of sections for receiving containers and a fluid transfer device is described.

Abstract: A blood collection system comprises a suction unit (11), a hose arrangement (12) connected to the suction unit, means for aspirating blood and air through the suction unit and for pumping said blood and air through the hose arrangement, a flow sensing unit (14) for continuously sensing the blood flow through the hose arrangement, an anticoagulant additive dosing system (15) for continuously dosing an anticoagulant additive into the blood flowed through the hose arrangement in response to the continuously sensed blood flow, a mixing unit (16) for mixing the blood with the anticoagulant additive dosed into the blood, and a collection vessel (17) for collecting the mixed blood and anticoagulant additive.

Abstract: An extracorporeal reservoir device including a housing, a venous inlet sub-assembly, and a venous filter. The venous sub-assembly is mounted to the housing and includes a downtube and a luer port connector body. The connector body extends from the downtube and forms a passageway open to a lumen of the downtube. The connector body is arranged such that fluid flow from the passageway merges with a flow path of fluid along the primary lumen at an angle of less than 90°. Secondary blood flow through the port connector body is less likely to induce turbulent flow into venous blood flow within the downtube, and is thus less likely to break up any bubbles carried by the venous blood. For example, at port flow rates of less than 500 mL/minute, fluid flow from the port connector body does not induce turbulent flow into fluid flowing through the primary lumen.

Abstract: A system for performing remote ischemic conditioning includes an inflatable cuff configured to encircle a limb of a subject and a controller removably attached to the cuff. The controller includes a pump; a manifold in fluid communication with the pump; a connector in fluid communication with the manifold and in removable fluid communication with the inflatable cuff; a pressure sensor; and a control circuit configured to implement a remote ischemic conditioning treatment protocol.

Abstract: A vacuum system is described for endoscopic intracavity, intraluminal or intracorporeal vacuum therapy, for aspirating body fluids, wound secretions or gases from a hollow volume, such as a body cavity, a hollow organ, a tissue abscess or an intestinal lumen, particularly in the production of a temporary endoscopic closure of an intestinal lumen. Based on this, many embodiments of an endoscopy arrangement are described.