Abstract: An implantable fluid router is described that includes one or more inlets, one or more outlets and at least one gas vent for removing gas from liquid routed from the one or more inlets to the one or more outlets, The implantable router may be used with implantable drug delivery apparatus. A catheter device including such a fluid router is also described.

Abstract: A control circuit for monitoring operation of an implantable blood pump, the control circuit operatively couplable to a testing apparatus for simulating blood pump operating conditions and testing the control circuit based on the simulated blood pump operating conditions. The control circuit includes an input module for receiving at least one of one of actual operating data from an implantable blood pump and simulated operating data from the testing apparatus. A processor for processing the received operating data is included, the processor configured to determine a source of the received operating data, and to determine whether the received operating data is actual operating data or simulated operating data based on the determined source.

Abstract: A catheter-based/intravascular ablation (denervation) system includes a multiplicity of needles which expand open around a central axis to engage the wall of a blood vessel, or the wall of the left atrium, allowing the injection of a cytotoxic or/or neurotoxic solution for ablating conducting tissue, or nerve fibers around the ostium of the pulmonary vein, or circumferentially in or just beyond the outer layer of the renal artery. The expandable needle delivery system is formed with self-expanding materials and include structures, near the end portion of the needles, or using separate guide tubes. The system also includes means to limit and/or adjust the depth of penetration of the ablative fluid into the tissue of the wall of the targeted blood vessel. The preferred embodiment of the catheter delivered through the vascular system of a patient includes a multiplicity of expandable guide tubes that engage the wall of a blood vessel.

Abstract: A medicament delivery device (10) comprises a medicament delivery mechanism including an injection needle (23). A housing (11) contains at least one component of the medicament delivery mechanism. A base plate (12) includes a contact surface (12b) for placement against a patient's body. The housing (11) is moveably connected to the base plate (12) and is moveable relative to the base plate (12) between a first position and a second position. The medicament delivery mechanism is operative upon movement of the housing (11) from the first position to the second position.

Abstract: Systems and methods for intelligently delivering fluid to a targeted tissue are described. The systems and methods may include directing a pump to distribute fluid to a targeted tissue and receiving one or more signals from an intracorporeal sensing system, where the one or more signals correspond to one or more sensed feedback parameters at the targeted tissue. The systems and methods may also include determining whether the one or more sensed feedback parameters are within an acceptable range. If the one or more sensed feedback parameters are not within the acceptable range, the systems and methods may include determining an adjusted velocity for the plunger necessary to adjust the pressure of the fluid in the pump so that the one or more sensed feedback parameters move within the acceptable range and directing the pump to distribute the fluid at the adjusted velocity.

Abstract: A device for delivering fluid to a user includes a housing, a drive motor assembly in the housing, a force sensor, and an electronics module. The drive motor assembly regulates delivery of fluid by actuating a piston of a fluid reservoir, and the force sensor generates output levels in response to force imparted thereto during, for example, fluid delivery operations. The electronics module processes the output levels of the force sensor to assess the operating health of the force sensor, to check for occlusions in the fluid delivery path, and to monitor the seating status of the fluid reservoir.

Abstract: Fluid injection devices and related systems and operating methods are provided. An exemplary injection device includes an actuation arrangement to facilitate delivering fluid from a container, a user interface element coupled to the actuation arrangement, a data storage element to maintain one or more patient-specific parameter values and historical bolus data, and a control module coupled to the actuation arrangement and the data storage element. The control module of the injection device determines a bolus amount of the fluid to be delivered based at least in part on the one or more patient-specific parameter values and the historical bolus data in response to receiving a user input indicative of a desire to administer a bolus, and the control module configures the actuation arrangement to automatically deliver the bolus amount in response to manual actuation of the user interface element.

Abstract: The invention relates to a jig for microneedle array placement that is provided with a main jig body with through holes through which the microneedles of the microneedle array will pass and a guiding part that guides the microneedle array to be incorporated into the main jig body and leads the microneedles into the through holes, and a microneedle array device using the jig for microneedle array placement. The invention prevents the deformation of the skin surface during puncture and allows penetration of the microneedles to the prescribed depth under the skin.

Abstract: A blood pump including a housing defining a proximal end, a distal end, and a first axis extending from the proximal end to the distal end. A ferromagnetic rotor is disposed within the housing and configured pump blood in a direction along the first axis. A stator is disposed within housing and around the ferromagnetic rotor, the stator is configured to apply a magnetic force causing rotation of the ferromagnetic rotor, the stator being eccentric to the rotor.

Abstract: An infusion pump and server computer have improved network access security. The infusion pump has a network interface circuit to provide communications over a network and a processing circuit that generates infusion pump data for transmission to a remote server computer. The processing circuit generates a header portion of a request message having at least one field, hashes the header portion but not payload data using a cryptographic hash function and a cryptographic key to provide a hashed code, and inserts the hashed code into the header portion of the request message. The processing circuit inserts the infusion pump data into a body portion of the request message and transmits the request message to the remote server computer over the communications network.

Abstract: A motorized drug delivery device configured to administer at least one pre-set dose of a medicament contained within a medicament container. The delivery device comprising a user activation system (13), a motor (22), a gear train (15) operatively coupled to the user activation system and the motor, and a piston plunger system (200) operatively coupled to the gear train. The piston plunger system comprises a piston plunger (50) and at least one plunger extension (42; 44) for extending a length of the piston plunger. The piston plunger system is configured to act on a stopper contained within the medicament container to deliver at least one pre-set dose of medicament. The user activation system comprises a mechanical automatic reset activation system for automatically resetting the drug delivery device after administration of the pre-set dose.

Abstract: The present invention relates to a medicament delivery device comprising a drive means configured to act on a medicament container for expelling a medicament; a holding means configured to hold said drive means in a pre-tensioned state; an activation means configured to interact with said holding means for releasing said drive means from the pre-tensioned state; wherein the device further comprises feedback means configured to interact both with said holding means and with said drive means for generating an audible and/or tactile and/or visual signal indicating that the medicament has been completely expelled.

Abstract: An improved diagnostic analyte monitoring device has partially retractable hollow guide needles for the intradermal placement of diagnostic elements fixedly connected to measuring means within this device obviating the need to remove the guide needle and to connect the diagnostic elements to measuring means after placement into the skin. A flexible surface adhering to the skin serves for the subcutaneous implantation of the diagnostic elements within the guide needles and partial retraction of the guide needles exposes the active surface to body fluid, actuated by means designed for easy handling and safe operation. Concentration-time profiles of endogenous and exogenous analytes measured with the device are used to improve drug treatment modalities on an individualized basis.

Abstract: A system for priming an infusion pump is disclosed. The system includes a priming cap including a septum and configured to matably connect with a male part comprising a needle and attached to a length of tubing for fluid, wherein when matably connected with the male part, the priming cap occludes the tubing.

Abstract: Systems and methods for delivering a medication to a person experiencing an emergency medical event without requiring intervention or action on the part of the person. A device encases a reservoir of medication and a delivery mechanism. Sensors in the housing sense a physical attribute of the person and circuitry monitors information collected by the sensors to determine if the person is experiencing a severe medical condition or event based on the information. An input device on or in the housing, such as a button, may be used or activated by the person if the detected condition or event is a false positive to cancel further action. If the system does not include the button or if the user does not press it in time, the system activates the delivery device and injects the medication into the person.

Abstract: An arrangement for connecting a syringe to an electromechanical pump for drug infusion is provided. The syringe comprises a syringe body having a first end for discharging a drug and a second end connected to the pump in a removable manner. An axially sliding plunger is housed in the syringe body for causing suction and injection of the drug through the first end. The pump comprises a pump body having a sliding rod that causes sliding of the plunger within the syringe body. The pump body has a collar axially extending around the sliding rod and provided with engaging elements. The syringe body has engaging elements arranged to cooperate with the engaging elements of the collar for firmly connecting the syringe to the pump. An annular flange extends radially around the syringe body. The flange cooperates with the collar to establish a tight sealing between the syringe body and the collar.

Abstract: A cannula device for the circulation of the blood in an artificial lung, includes: an aspiration lumen including at least one orifice permitting the aspiration of a volume of blood; an injection lumen including at least one orifice permitting the injection of a volume of blood, wherein the injection lumen and the aspiration lumen are held rigidly connected over at least a portion of their length, the lumens being sealed in relation to each other, the injection lumen having a deformable element, which is held on a portion of the distal end thereof, the deformable element having a first setting and a second setting, the change from the first setting to the second setting being effected by a modification of the diameter of the deformable element.

Abstract: A syringe is disclosed, which includes a needle having an outer cylinder including an outer cylinder body part and a needle fixing part provided at a distal end part of the outer cylinder body part; an injection needle 6 having a puncturing needle tip at a distal end and fixed to the needle fixing part; and a gasket housed in the outer cylinder. The injection needle is such a tapered part holding injection needle that a puncturing time piercing part having a needle tip has an outer diameter of 0.42 mm or less and has a thickness of 0.1 mm or less, or the injection needle is such a small diameter thin injection needle as to have a thickness of 0.04 mm or less. The gasket includes a gasket body and a soft coating provided on a portion that comes into contact with the inner surface of the outer cylinder.

Abstract: The invention relates to a control device suitable for suggesting control instructions to the patient in order to facilitate the use thereof.

Abstract: The present invention uses an injection apparatus comprising: an injector which includes a mounting part on which a syringe is mounted, a needle assembly having a plurality of needles, a motor and a screw for actuating a piston of the syringe forward and backward; and a main body for controlling the forward and backward actuation of the piston of the syringe and drug injection. The present invention is configured as follows: a vacuum suction pressure is formed in the needle assembly that is in contact with the skin; injection is performed so that a drug is injected through a needle after it is determined that the needle is in close contact with the skin by comparing a sensed vacuum suction pressure value with a preset vacuum suction pressure value; and if injection is completed, the needle assembly is separated from the skin.

Abstract: Systems, methods, and apparatuses are provided for delivering reduced pressure to a subcutaneous tissue site, such as a bone tissue site. In one instance, a manifold for providing reduced pressure to a subcutaneous tissue includes a longitudinal manifold body formed with at least one purging lumen and a reduced-pressure lumen. The manifold further includes a plurality of manifolding surface features or slits formed on the second, tissue-facing side of the longitudinal manifold body and a plurality of apertures formed in the longitudinal manifold body on the second, tissue-facing side. The plurality of apertures fluidly couple the reduced-pressure lumen and the manifolding surface features or slits. The manifold further includes an end cap fluidly coupling the reduced-pressure lumen and the at least one purging lumen. Other systems, apparatuses, and methods are presented.

Abstract: A wearable, conductive textile patch is provided that may include any of a number of features for monitoring body analytes and/or delivering fluids to a body. In one embodiment of the invention, a single, patch-mounted system monitors glucose levels of a diabetic person and provides appropriate doses of insulin in response to the glucose measurements. A hand-held user interface can be provided for wirelessly controlling the system and/or receiving information from it. Conductive pathways can be formed in the fabric of the patch. Components that can be integrated into the flexible patch include a power source, controller, transmitter, antenna, temperature and other sensors, fluid pump, infusion set, electrical pathways, switches, controls, electrodes, connectors, resistors and other circuit elements. Such components can be embedded, interwoven or coated on to the flexible patch instead of or in addition to surface mounting. Methods associated with use of the flexible patch system are also covered.

Abstract: A method of manufacturing a hermetic lead connector includes fixing an electrically insulating ring between an electrically conducting contact ring and an electrically conducting spacer ring to form a hermetic ring subassembly, and fixing a plurality of the hermetic ring subassemblies in axial alignment to form a hermetic lead connector. The hermetic lead connector includes an open end, an outer surface, and an inner surface defining a lead aperture. The hermetic lead connector provides a hermetic seal between the outer surface and the inner surface.

Abstract: An auto-injection device including a housing, cartridge, needle, and needle cover. The housing includes longitudinally extending flexible arms. The cartridge moves relative to the housing and contains fluid medicament. The needle is at a proximal end of the device. The needle cover has openings along the longitudinal direction and moves between a first position, a second position, and a third position, wherein the needle is unexposed in the first and third positions and in the second position the needle is exposed. The needle cover is biased towards the third position. An abutment on the at least one longitudinally extending arm of the housing is receivable within the at least one opening along the longitudinal direction of the needle cover when the needle cover is biased into the third position.

Abstract: A device and a method for prevention of hypoglycemia are disclosed. In one aspect, the device and the method for prevention of hypoglycemia can comprise receiving a target blood glucose (TBG) level corresponding to a desired level of glucose in a patient's body during a fasting time period; receiving a bedtime blood glucose (BBG) level corresponding to a level of glucose in the patient's body substantially at a beginning of the fasting time period (e.g. before bedtime); receiving a first set of parameters corresponding to a medical state of the patient; determining a therapeutic course of action based on the levels of the TBG, BBG and the medical state of the patent; and administering the therapeutic course of action to the patient.

Abstract: An infusion system having an integrated inserter and infusion set (10) for containing and placing a flexible catheter (40), and a retractable introducer needle (26), wherein the catheter (40) is isolated from movement after placement. The integrated inserter and infusion set (10) includes a hub (20), having a user push button (30) to activate the device for catheter (40) placement. An adhesive liner (34) can be provided to cover an adhesive layer (36), such as pressure sensitive adhesive (PSA), on the bottom of the device (10).

Abstract: A pharmaceutical injection device includes a main body case, a cartridge holder, a latching receiver, a driver, and a manipulation component. The cartridge holder has a holding space and a holder latching component. The holding space is capable of holding a pharmaceutical cartridge. The latching receiver is configured to latch or release the holder latching component according to whether the cartridge holder is closed or open. The driver is configured to automatically release a latching of the latching receiver and the holder latching component. The manipulation component is configured to manually release the latching of the latching receiver and the holder latching component by moving the latching receiver upon being subjected to external pressure. The driver or the manipulation component is configured to release the latching between the latching receiver and the holder latching component.

Abstract: The invention relates to a compressible and expandable blade (2) for the rotor of a fluid pump (30) having at least two lamellae (3, 4, 5) which are disposed adjacently, are pivo table respectively relative to an axis of rotation (Ia) of the rotor and moveable relative to each other, and abut against each other in the expanded state of the blade such that they form together a continuous blade surface.

Abstract: The present invention relates to a medicament delivery device comprising a generally tubular distal housing part (10; 110) having opposite proximal and distal ends, wherein third mechanically coded interface means (11; 111) are arranged on its proximal end; a generally tubular proximal housing (20; 120) part having opposite proximal and distal ends and being releasibly connected to said distal housing part, wherein with fourth mechanically coded interface means (22; 122) are arranged on its distal end; a medicament container having a slidable stopper, wherein said container is arranged to be positioned within said proximal housing part; a plunger rod (60; 160) arranged within said distal housing; drive means arranged within said distal housing and being operably connected to said plunger rod for driving said plunger rod and thereby said stopper towards the proximal end of the device; wherein said device further comprises an interface member (50; 150) comprising first (51; 151) and second (52; 152) mechanicall

Abstract: A medication injection device (2) includes a housing (4) and a needled syringe (8) supported by the housing. The needle syringe has a plunger (10) and a volume containing medication. The medication injection device further includes an expelling mechanism (6) operably coupled to the plunger. Additionally, the device includes a thermal locking mechanism (20) operably coupled to the expelling mechanism, comprising a material which is solid when the device is refrigerated and transitions to a liquid or gel-like state at a phase-change temperature when the device is taken out of refrigeration and warms up together with the contained drug to a temperature which is suitable for performing an injection. In the solid state, the material keeps the expelling mechanism locked in a disabling condition inhibiting delivery of the medication and in its liquid state creates an enabling condition permitting delivery of the medication.

Abstract: The present invention concerns a drive mechanism (3) for a drug delivery device (1), which comprises a piston rod (40) comprising a first piston rod member (7) and a second piston rod member (8). The drive mechanism (3) further comprises an adjustment member (9). The drive mechanism (3) has a first state in which the first and the second piston rod member (7, 8) are moveable with respect to each other by operating the adjustment member (9), thereby adjusting the length of the piston rod (40), and wherein the adjustment member (9) is arranged at least partially inside the second piston rod member (8). Moreover, the present invention concerns a method for assembling the drug delivery device (1).

Abstract: An injection device for administration of an injection to an animal can include a main body, which contains an injection instrument, a contact device, which has a contact area which is shaped in conformity with a body part of the animal to which the injection is to be administered. A support device which supports the contact device on the main body can be movable in a pressure application direction. A force measurement device including at least one force sensor can be designed to measure at last one force with which the contact device acts on the main body. A control device can activate the injection instrument if the force measured by the force measurement device lies in a specified range.

Abstract: A user-wearable patch pump system for delivery of insulin or other medicament can include a pump and an attachment portion that attaches the pump to a user's body. The pump can include a drive unit and a disposable cartridge containing a medicament with the drive unit configured to cause the pump to deliver the medicament in the cartridge to the user. The attachment portion can include a retention frame configured to selectively retain the pump therein and an adhesive patch configured to be attached to the user's body. The pump can be selectively attached to the retention frame and used to deliver medicament through tubing to an infusion site displaced from the pump.

Abstract: An infusion system for infusing a liquid into a body includes an external infusion device and a remote commander. The external infusion device includes a housing, a receiver, a processor and an indication device. The receiver is coupled to the housing and for receiving remotely generated commands. The processor is coupled to the housing and the receiver to receive remotely generated commands and to control the external infusion device in accordance with the commands. The indication device indicates when a command has been received and indicates when the command is being utilized to control the external infusion device so that the external infusion device is capable of being concealed from view when being remotely commanded. The remote commander includes a commander housing, a keypad for transmitting commands, and a transmitter for transmitting commands to the receiver of the external infusion device.

Abstract: Systems for managing pressure in a fluid reservoir chamber of a fluid infusion device are provided. For example, a fluid infusion device comprises a housing having a reservoir chamber that receives a fluid reservoir and a pump chamber. The fluid infusion device also includes a drive system contained within the pump chamber, and the drive system includes a slide that is movable relative to the fluid reservoir. The slide includes a proximal slide end that cooperates with a portion of the fluid reservoir to dispense fluid, and the proximal slide end has a projection. The fluid infusion device includes a pressure management system defined in the projection of the slide. The pressure management system includes at least one bore defined through the projection. The at least one bore is spaced a distance apart from a perimeter of the projection to vent air from the reservoir chamber into the pump chamber.

Abstract: An infusion set has a partially integrated ballistic inserter that can insert a needle at a controlled rate of speed to a depth to deliver content to the upper 3 mm of skin surface, and a skin-securing adhesive layer to secure the skin surface at the insertion site such that the inserter that can insert a needle with a reduced risk of tenting of the skin surface. A removable turnkey or pushable handle can be provided to release a driving spring of the ballistic inserter to insert a needle at a controlled rate of speed, of 3.3 ft/sec. (1.0 m/sec.) up to and including those greater than 10 ft/sec. (3.0 m/sec.), then release from the set for disposal. The infusion set can further include an extendable interface ring that retracts when the inserter is removed from the infusion set.

Abstract: Provided is a treatment method and a medical device that can intentionally and locally administer a drug to a lesion area appearing in a narrow blood vessel such as a retinal blood vessel and a spinal blood vessel. The treatment method has an introduction step of introducing a medical elongated body having a drug holder for holding a drug into a living body, an arrangement step of arranging the drug holder at a treatment target inside the living body, and a discharge step of discharging the drug to the treatment target by releasing the drug held by the drug holder.

Abstract: Various embodiments disclosed herein relate to needle-based injectors that incorporate a power assembly comprising a stored energy source and a rate control assembly. The power assembly may be further configured to allow the injection to be performed with more force than a user may be capable of delivering, while also allowing the user to maintain control of the injection process after the stored energy source has been released and the injection has begun, such the user may increase or decrease the rate of injection, or stop the injection, during the injection process. In various embodiments, the power assembly may comprise spring- or gas-based stored energy sources, and/or may comprise friction- or tension-based rate control assemblies. Described herein are also methods for injecting an agent using embodiments of the devices described here.

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: 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 pressurizable fluid supply apparatus may include a bag to hold a fluid. The bag may include a fluid outflow interface and a bladder positioned adjacent to the bag. The bladder may include a plurality of chambers positioned vertically in series. Adjacent chambers may be separated by dividers. The dividers may be configured to allow fluid flow between adjacent chambers under specified conditions. The bladder may further include a pressure inlet positioned at a top of the bladder.

Abstract: A medical device system is disclosed. The medical device system includes a first medical device and a second medical device. A remote interface including a touch screen is also included. The remote interface is in wireless communication with the first medical device and the second medical device. The remote interface is configured to provide a user interface to the first medical device and the second medical device. The remote interface is configured to receive user input through a touch screen. Also, a charging device is included. The charging device is configured to receive at least the first medical device and the remote interface and the charging device is configured to recharge a first medical device battery and the charging device is configured to recharge an interface battery in the remote interface. The charging device is connected to a personal computer wherein the personal computer provides information to the remote interface.

Abstract: A fluid delivery device includes: a first chamber configured to receive fluid from a fluid reservoir; a second chamber configured generate a vacuum therein to apply pressure to the fluid in the first chamber to enable the fluid in the first chamber to be output from the fluid delivery device; and a flow control member configured to allow the fluid in the first chamber to flow through the flow control member into the fluid reservoir at a predetermined flow rate to decrease the vacuum in the second chamber.

Abstract: A means and a method is disclosed to diminish or eliminate pain associated with a sharp object penetrating skin, during such procedures as an injection, biopsy, or deriving a blood sample. To this end, repeated tapping, pressing, or rubbing is performed over the skin at or near a site of penetration of the sharp object in conjunction with applying electricity on the skin. The invention discloses a method of using a syringe or a lancet, with enhanced features, to provide local anesthesia at a site of penetration of a sharp object.

Abstract: A medicament delivery system, including a medicament container and a delay mechanism that is activated prior to completion of medicament delivery from the medicament container. The delay mechanism automatically activates a subsystem or initiates an operation subsequent to completion of medicament delivery.

Abstract: Infusion systems, infusion devices, and related operating methods are provided. An exemplary method of operating an infusion device to deliver fluid to a body of a user involves identifying a current site location on the body of the user associated with a sensing arrangement providing sensed measurements of a physiological condition in the body of the user at the current site location, determining one or more performance metrics associated with the current site location corresponding to operation of the infusion device to deliver the fluid in response to the sensed measurements, and providing sensor site feedback in a manner that is influenced by the one or more performance metrics. In one or more embodiments, the sensor site feedback includes recommended sensor site locations for rotation or replacement of the sensing arrangement determined based on historical data associated with the user for different sensor site locations.

Abstract: A medical device system. The system includes a first medical device, a first remote interface, and a second remote interface in communication with the first remote interface and the first medical device, wherein the first medical device sends a command to the first medical device through the second remote interface, and wherein when the second remote interface receives the command, the command must be confirmed by the second remote interface before the command is send by the second remote interface to the first medical device.

Abstract: A cannula insertion device is disclosed. The device includes a needle carriage, a rail device on which the needle carriage is slidable, a yoke having a channel, a linkage connected to the needle carriage and extending into the channel, a torsion spring with one end connected to the linkage, and locking device for locking the torsion spring in tension and maintaining the needle carriage and the linkage in a locked position prior to activation. Upon release of the locking device, the tension of the torsion spring is released, which causes the linkage to move in the channel and slide the needle carriage along the rail device. A catheter carriage may also be provided for actuation by the linkage.

Abstract: An injection device is disclosed which comprise a housing (10), a plunger (40) for expressing a medicament from a syringe (20) and an actuation mechanism (30). The actuation mechanism (30) is arranged in use to move the plunger (40) between a first rearward position and a second forward position to express a dose from the syringe (20). The injector device further comprises an injection activation sensor 51, arranged for example to provide an end of dose indication. The sensor 51 comprises an elongate flexible member (50). The flexible member (50) has a first end (52) connected to the plunger (40) or actuation mechanism (30) such that actuation motion of the injection device acts to move the elongate flexible member (50) relative to the housing. Movement of the elongate member (50) triggers a response to the injection such as an audible and/or tactile injection complete indication.

Abstract: A catheter pump comprising a pump head for insertion into the aorta. The pump head includes: a rotor having propellers that can be displaced from a folded insertion position in which the pump head can be inserted into the aorta, to an unfolded operating position in which the rotor can be set in rotation, and a cage surrounding the propellers. The cage comprises a distal, proximal sheath and filaments running between sheaths. The sheaths are moved towards one another at or before the unfolding of the propellers in a manner that the regions of the filaments lying between the sheaths expand radially outward, to form a space surrounding the unfolded propellers. At least some or all of the filaments are configured so as to each have at least one main section that engages one sheath and splits into at least two minor sections in the direction toward the other sheath.