Abstract: A portable exercise device for the posterior muscle chain. The portable exercise device can include a first anchor and a second anchor, the anchors being oriented substantially vertically, and at least one central member coupled to and extending between the first anchor and the second anchor. The anchors can include a housing, a handle portion rotatably disposed at a first end of the housing, and an anchoring portion operatively coupled to the handle portion and disposed at a second end of the housing.

Abstract: A machine tool is provided with a chain-type bit-storing apparatus which includes a frame, two sprockets, a chain and a pivoting unit. The frame includes a cutout. The sprockets are placed in the frame. The chain is driven by the sprockets. The chain includes links each including a socket for containing a bit, two plates for supporting the socket, first and second blocks placed between the plates, first and second bearing units for rotationally supporting the first and second blocks on the plates, and a connecting unit for pivotally connecting the first block thereof to the second block of an adjacent link. The pivoting unit is used to pivot the socket of a selected one of the links to move an open end of the socket out of the frame through the cutout.

Abstract: A cyclomagnetic device for use in cyclomagnetic therapy. The device has a head and tail connected by a handgrip and is housed in housing in the shape of a showerhead. Inside the head end, a variable speed DC motor turns a rotor to which magnets are attached in a unipolar and unbalanced arrangement so that the rotor vibrates when the rotor turns. Inside the tail end is a pressure/trigger point massage tool. A battery pack that provides power to the motor is located in the handgrip. A dual switch attached to an electronic card connects the batteries to the motor that operates the device. To provide comfort when the device is used on the body, a soft rubber cushioned band is provided around the edge of the head and a soft rubber boot covers the tail of the device.

Abstract: A method of manufacturing a composition for enlarging the penis comprises the steps of picking the auto-tissue of a skin from the abdomen or flank region of a patient; (2) obtaining a purified mixture of the dermis and fat by removing the red blood cells of a lower layer from the auto-tissue through centrifugation; (3) separating and extracting stem cells from part of the purified mixture; (4) picking blood from the patient and purifying the blood through centrifugation; (5) extracting a Platelet Rich Plasma (PRP), including rich growth factors, from the purified blood; and (6) fabricating the composition by mixing the mixture obtained at the step (2) and not used to extract the stem cells, the stem cells, and the Platelet Rich Plasma (PRP).

Abstract: A system for sexual stimulation includes a first sexual stimulation device having a first sensor and a first actuator and a second sexual stimulation device having a second sensor and a second actuator. The first sexual stimulation device is configured to communicate information from the first sensor to actuate the second actuator of the second sexual stimulation device and the second sexual stimulation device is configured to communicate information from the second sensor to actuate the first actuator of the first sexual stimulation device.

Abstract: Dilators with a threaded distal portion and direct visualization capability may be used for penetrating and dilating stiff tissues and bones. The threaded portion of a dilator engages the tissue between the insertion site and the target site, and may be rotated for advancing through the target tissue in a more controlled fashion. The direct visualization capability may be used to visualize the ligament as the threaded distal portion passes through the ligamentum flavum. The devices and methods described may be used in procedures, for example, where ligaments surrounding the epidural space need to be dilated in order to deliver one or more surgical instruments into the epidural space.

Abstract: An endoscopic image pickup unit includes: a first fixed lens frame which holds a first objective lens group; a second fixed lens frame which, being fitted over the first fixed lens frame, holds a second objective lens group; a movable lens frame which, being installed in the second fixed lens frame so as to be able to move forward and backward along a photographic optical axis, holds a movable lens; and a deformation preventing member which, being interposed between a distal end body and the second fixed lens frame, prevents the second fixed lens frame from being deformed by fixing force of the fixing member when the endoscopic image pickup unit is fixed to the distal end body.

Abstract: An endoscope gas feed system includes a fluid curtain nozzle for blowing a fluid curtain-forming gas toward an observation window provided on a distal end surface of the insertion part of an endoscope, the distal end surface including at least the observation window and an opening for spraying a constant-pressure feed gas, and the fluid curtain nozzle is provided on an opposite side of the opening with respect to the observation window, a gas/water feed nozzle for cleaning the observation window, the gas/water feed nozzle being provided on the distal end surface, a constant-pressure gas feed unit for supplying the constant-pressure feed gas, so as to spray the constant-pressure feed gas from the opening, and a fluid curtain-forming gas feed unit for supplying a gas, so as to blow the fluid curtain-forming gas from the fluid curtain nozzle.

Abstract: An endoscope 100 includes a first light source 45 that emits white illumination light, a second light source 47 that emits narrow-band light and an imaging section that has an imaging device 21 having plural detection pixels and images a region to be observed. The imaging section is caused to output a captured image signal including both a return light component of the white illumination light from the region to be observed by and a return light component of the narrow-band light the white illumination light. From the captured image signal, the return light component of the narrow-band light is selectively extracted, and a brightness level of the extracted return light component of the narrow-band light is changed by changing a light amount of light emitted from the second light source 47.

Abstract: A self-retaining retractor and surgical method of retracting integument at a surgical site comprising a medial arm moveably connected to a first end of an extension arm. The extension arm is connected to a lateral arm. The connection may be made after the medial arm is in the surgical site. The extension arm may be moved from an undeployed position to a deployed position. The medial arm or the lateral arm may include a surgical instrument holder, such as a holder for an endoscope. A locking mechanism may be used to lock the retractor in a deployed position. A strap may also be used to secure the retractor.

Abstract: An eyelids opening device with a drape comprising a flexible upper ring (1) applied in contact with the face while surrounding eyelids, a lower ring (2) inserted into a conjunctiva sac and applied in contact with the eyelids conjunctiva side, and an elastic sheet (3) of soft tubular thin film located to extend from the face side to the eyelids conjunctiva side and used to fix one end to the upper ring and to fix the other end to the lower ring by expanding, wherein the outside diameter at the smallest portion of the elastic sheet is substantially equal to or longer than the interpalpebral length (between upper and lower eyelids). Difference in size of conjunctiva sac or interpalpebral length of individuals is absorbed even by an appliance of one size, the eyelids can be opened by fitting the eyelids opening device to the eyelids or the face while burden on the eyeball is reduced and high safety is ensured.

Abstract: An illuminated suction apparatus including a hand-held surgical device combining a high-performance non-fiber optic optical waveguide with suction. This device is useful in a wide array of surgical procedures including open and minimally invasive orthopedics.

Abstract: A physical activity data collection unit includes one or more infrared sensors configured to provide an output indicative of a pulse rate of a user of the physical activity data collection unit, at least one temperature sensor configured to provide an output indicative of at least a body temperature of the user, and at least one accelerometer configured to provide an output indicative of movements of the user.

Abstract: Embodiments of the present disclosure are configured to visualize severe blockages in a vessel and, in particular, chronic total occlusions in blood vessels. In some particular embodiments, the devices, systems, and methods of the present disclosure are configured to visualize the blockage to facilitate safe crossing of the blockage.

Abstract: The invention relates to a method for ultrasonic imaging of an organ in a patient's body through a part of the patient's respiratory tract, including: arranging an ultrasonic imaging device in or on the patient's body; introducing a flexible catheter carrying at least one inflatable member into the respiratory tract; positioning the inflatable member at a predetermined location in the respiratory tract; filling the inflatable member with an ultrasonic transmission fluid through the flexible catheter; and transmitting ultrasonic waves from the imaging device through the transmission fluid in the inflatable member to the organ to be imaged. The inflatable member is positioned in the respiratory tract by manipulating guide means that are attached to or integrated with the flexible catheter. The invention further relates to an ultrasonic imaging system for carrying out this method and to an assembly means for use in such an ultrasonic imaging system.

Abstract: A clinical decision support system for patient treatment having a monitoring device operably coupled to a patient. The monitoring device outputs a monitoring signal in response to a measured parameter of the patient. A controller receives the monitoring signal and outputs a display signal. The controller further compiles clinical documentation relating to the patient based on the monitoring signal and outputs a documentation signal related thereto. A display device then receives the display signal and the documentation signal and displays the same in connection with various indicia thereby displaying both the monitored signal and associated clinical documentation.

Abstract: A respiration pattern of a number of respiration cycles is detected and breath intervals (BI) and tidal volume (TVOL) measurements of each of the respiration cycles are respectively determined. An unevenly sampled instantaneous minute ventilation (iMV) signal is produced using the BI and TVOL measurements, and an evenly sampled iMV signal (resampled iMV signal) is produced using the unevenly sampled iMV signal. Disordered breathing is detected based on a comparison between a baseline threshold and the resampled iMV signal.

Abstract: A punch biopsy device is disclosed with an integrated tissue base cutting component. In an embodiment, the punch biopsy device includes a cutting blade with first and second arms operatively coupled to a handle. The punch biopsy device includes a prong flexible and integral to the cutting blade, the prong comprising top and lateral sharp edges configured to pierce and cut tissue, respectively. The prong is configured to be inserted into a body in a neutral position with the prong parallel with the first and second arms. The prong is configured to move to a position perpendicular to the first and second arms when the cutting blade is withdrawn to allow for the prong to catch and pierce the tissue. The prong is configured to cut the tissue while in the position perpendicular to the first and second arms when the cutting blade is rotated manually via the handle.

Abstract: Medical devices for navigation through anatomy, including guidewires, which may have a core wire, a slotted tubular member, or both. Embodiments may have coils, including non-circular cross-section edge-wound marker coils, extended coil tips, and soldered or glued mesial joint coils. Core wires may have a step, ridge, or taper at the joints to the tubular member, and may be flattened at the distal tip. Radiopaque material may be located inside the tubular member, and the distal tip may be heat treated to make it shapeable. Additional tubular members or coils may be used concentrically or in line and may enhance flexibility, provide radiopacity, reduce friction, or reduce material or manufacturing cost. Tubular members may be chamfered or tapered continuously or incrementally. Slots may be arranged in groups, such as groups of three, and may be equal in depth or unequal in depth to provide a steerable or compressible tip.

Abstract: A flexible guidewire comprising a hollow tube, having a proximal section and a distal section, the distal section having a distal tip, the outer diameter of the distal section gradually decreasing toward the distal tip, the outer diameter of the distal tip being larger than the smallest outer diameter of the distal section, the flexible guidewire further comprising a plug coupled with the distal tip of the hollow tube for creating a non-traumatic tip, and the flexible guidewire further comprising a tubular spring, being place around the distal section of the hollow tube for maintaining the outer diameter of the hollow tube over the length thereof and for supporting compressive loads.

Abstract: A system for treating arthritis includes at least one joint stabilizing assembly for providing relief from arthritis. At least one signal transmission element engagement member is operatively connected to the joint stabilizing assembly for connecting a signal transmission element. At least one signal transmission element is supported by the at least one signal transmission element engagement member. An electrostimulation unit, electrically connected to the signal transmission element produces a signal for improving the overall function of an arthritic joint. The electrostimulation unit used in conjunction with the joint stabilizing assembly provides a synergistic effect, which results in optimized joint treatment versus using either the joint stabilizing assembly or electrostimulation unit alone.

Abstract: A pet ear cleaning device is disclosed for gently cleaning an animal's ears. The device can be used for home or veterinary use. The pet ear cleaning device comprises a nozzle, a liquid reservoir in fluid communication with the nozzle, an internal pump assembly, and a tip for cleaning a pet's ear. A user would press a manual dispensing component which would activate the internal pump assembly which would then draw fluid from the liquid reservoir and transfer it to the nozzle. The liquid reservoir is typically a reusable reservoir that a user would re-fill with ear cleaning solution when empty, or it can be a replacement cartridge. Further, the nozzle typically comprises threads on its end for retaining the cleaning tip on the nozzle. After use, a user would discard the tip via a manually operated discard component that allows a user to remove the soiled tip hands free.

Abstract: A method for connecting medical tubing or any other type of fluidic circuit conduits (e.g., cannulae) to a ventricular assist device (“VAD”) or any other pumping device used for blood pumping during cardiac circulatory support for vascular surgery. The method prevent air bubbles from entering a cardiac circulatory support system when connecting cannulae to a VAD that may later enter the blood stream of a patient during cardiac surgery, and also provide for purging any air bubbles that may have entered the cardiac circulatory support system during a cannulae-VAD connection.

Abstract: A bio-compatible lumen bearing device such as a catheter formed of a polymeric material having a titanium surface bonded to the underlying exposed catheter surface. The titanium surface is employed in patients to improve bio-compatibility and enhance lubricity during insertion and removal.

Abstract: An infusion system to administer a fluid includes an infusion pump with a pump processor, a pump memory to store a plurality of configurable alarms and a pump radio to enable bi-directional communication. The infusion system further includes a controller that has a controller processor, a controller memory, a controller radio to transmit and receive communication from the pump radio. The controller further has a graphical user interface shown on a display along with controls to manipulate the graphical user interface. Furthermore, the bi-directional communication between the infusion pump and the controller establish an infusion pump relative proximity between the infusion pump and the controller such that when the infusion pump relative proximity exceeds a pump threshold distance at least one of the plurality of configurable alarm conditions of the infusion pump is modified.

Abstract: Apparatus and methods for treatment of an internal cavity are provided. The internal cavity is coated with a treatment solution. The treatment solution can include a solidifiable matrix with or without a drug or combination of drugs incorporated therein, or a drug solution without a solidifiable matrix. The treatment solution is coated onto at least a portion of the internal cavity, and acts as a slow-release drug delivery system.

Abstract: Balloon systems for treating bifurcated lumens include desirable burst and folding characteristics. In some cases, the balloon systems can be formed by varying the wall thickness of a balloon parison.

Abstract: A controlled volume inflation-deflation device to inflate a balloon to occlude a blood vessel by dialing a knob that locks at rotational positions to locate a plunger at equally spaced locations within a syringe of the inflation-deflation device. The inflation-deflation device includes a releasable latch to lock the proximal and distal housings together to hold the plunger forward for occlusion, and to separate and hold the proximal and distal housings to retract the plunger for perfusion. When the inflation-deflation device is returned to the latched position, the balloon is re-inflated to its previous occlusive diameter. Also, an extension tube made of a lower modulus outer material co-extruded over and miscible with a higher modulus inner material may be used to produce a suitably low compliance extension tube for the inflation-deflation device.

Abstract: A safety needle locking device, which may be used with a syringe, consisting of a Blunting Member (19). The Needle (16) has a Needle Curvature (25) which allows locking of the Blunting Member (19) within the needle with the indent (27). The blunting member also has a Puncture Tip Protector (26) which allows for the Needle Tip (24) to be sheathed upon expulsion of the fluid. The needle is tubular with one surface flattened out. The Blunting Member is aligned within the needle. When the fluids are expelled the blunting member moves out, blocks the needle tip and locks inside the needle. Thus preventing reuse and needle stick injury. The syringe is flattened along one longitudinal surface to allow for alignment.

Abstract: The present invention provides a safety syringe which resolves a problem in the prior art whereby the needle assembly does not engage the plunger properly due to limitations in the syringe protrusion molding. The syringe of the present invention comprises: a cylinder which has a space therein to contain fluid and forms a fluid discharging portion at one end; a plunger which is inserted inside the cylinder and slid in a longitudinal direction; a piston which is associated with the upper portion of the plunger in order to make airtight contact between the plunger and the cylinder; a syringe needle assembly which is equipped at the upper portion of the cylinder and affixes a syringe needle. The syringe needle assembly is inserted into and contained inside the cylinder after use and is then disposed. In the needle assembly, plural needle supports comprising a first connector and a second connector are extended to the lower portion.

Abstract: The invention is an apparatus comprising of a syringe, a plunger and a circuit for the purpose of activating a light source to illuminate a target area for application of the contents of the syringe in low-light or no-light situations.

Abstract: Included are embodiments of an ambulatory infusion device. Some embodiments include a battery receiving portion that receives a user-replaceable battery of variable individual characteristics. The user-replaceable battery may serve as a primary power source of the ambulatory infusion device and being successively depleted during application. Similarly, some embodiments include a dosing unit with an electrically powered actuator and an electronic controller that controls operation of the ambulatory infusion device. Still some embodiments include a testing unit that is operatively coupled to the electronic controller, the testing unit being designed to carry out a battery test, the battery test including determining an off-circuit voltage and an internal resistance of the user-replaceable battery. Still some embodiments include an alerting unit that is operatively coupled to the testing unit and/or the electronic controller to provide an alert to a device user in dependence of a battery test result.

Abstract: An infusion pump for delivering medicament to a user. The pump comprises a pump mechanism and a bolus program module. The bolus program module is programmed to control the pump mechanism to deliver a bolus. An alarm program module is in data communication with the alarm, the timer, and the bolus program module. The alarm module is programmed to generate an alarm signal when the bolus program module does not control the pump mechanism to deliver a bolus within a predetermined period of time.

Abstract: A drug delivery pump drive which uses a linear piezoelectric motor to advance a syringe piston to deliver a liquid drug and a method thereof are disclosed. The pump drive, provided in a drug delivery pump, provides silent operation and very low energy consumption compared to electric motor-based drives. The small size of the motor helps also to reduce overall size of the pump drive and the resulting drug delivery pump.

Abstract: A needle tip shielding mechanism is described herein. The shielding mechanism comprises an outer housing, an inner housing, and a needle having a needle feature. Generally, the outer housing comprises at least one adapter-interlock feature. Moreover, the inner housing comprises a needle-feature capture mechanism, such as a washer feature, and a needle-tip capture mechanism, such as duckbilled tip barrier. In some cases, the inner housing is slidably moveable within the outer housing. In such cases, the inner housing is movable between a first position that biases the adapter-interlock feature into an engaged position and a second position that allows the adapter-interlock feature to move to an unengaged position. This ability to bias the interlock feature in the engaged position and to allow the interlock feature to move to the unengaged position allows the shielding mechanism to be selectively coupled to and released from an interlock-feature mating component within a catheter adapter.

Abstract: Some embodiments of a medical device anchor system include an anchor device that receives a catheter (or other medical instrument) and secures the catheter in place relative to a skin penetration point. In some embodiments, the anchor device can secure the catheter in an operative position relative to the skin without the use of sutures or skin tapes. In particular embodiments, the anchor device can be adjusted to a folded condition so that subcutaneous anchors are partially rotated prior to removal from the skin penetration point.

Abstract: Described herein are syringe devices, systems and methods. In general, the syringe may include a first chamber and a cartridge movable within the first chamber. The cartridge may include a cartridge chamber and a valve in fluid communication with the cartridge chamber and the first chamber and having an open configuration and a closed configuration. The valve may allow movement of a liquid out of the cartridge chamber while in a open configuration. The cartridge may also include a second end, movable within the cartridge chamber, and a locking mechanism having a locked configuration and an unlocked configuration, the locking mechanism preventing movement of the second end within the cartridge chamber while in the locked configuration.

Abstract: A medical injector is provided herein having a body with a displaceable plunger. The plunger includes a plurality of spaced-apart ratchet teeth disposed along the length thereof. At least one indexer is provided formed to engage the plunger, wherein the indexer is configured to allow the plunger to displace distally towards a distal end of the body but not proximally towards a proximal end of the body. The medical injector also includes an actuator having an engagement portion formed to engage one or more of the ratchet teeth. The actuator is displaceable to a ready state, the engagement portion being displaced proximally relative to the plunger with the actuator being displaced to the ready state. The indexer prevents proximal movement of the plunger thereby allowing the engagement portion to by-pass one or more of the ratchet teeth with the actuator being displaced to the ready state. In addition, the actuator is displaceable from the ready state to cause actuation of the medical injector.

Abstract: A fluid transfer device with a fluid transfer device housing, including a bore and a valve seat that extends around the bore, configured to be carried within the implantable medical device, a piston located within the bore, and a valve element movable relative to the valve seat. One of the valve seat and the valve element includes a main portion and a seal portion that is less tacky than the main portion and is in contact with the other of the valve seat and the valve element when the valve element is in the closed position.

Abstract: An implantable medical device with a reservoir including a movable reservoir member, a fill port in fluid communication with the reservoir, and a valve that includes a housing including an opening in fluid communication with the fill port and the reservoir and a valve seat adjacent to the opening, and a valve element, operably connected to the movable reservoir member, that is movable relative to the valve seat between a closed position and an open. One of the valve seat and the valve element includes a main portion and a seal portion that is less tacky than the main portion and is in contact with the other of the valve seat and the valve element when the valve element is in the closed position.

Abstract: A catheter having a catheter body with a lumen and a distal lumen opening. The catheter's lumen extends through the catheter body along a longitudinal axis of the catheter body. A spiral slit is formed through a wall of the catheter body.

Abstract: An apparatus comprises a port, a catheter, a sleeve in communication with the catheter, and an alignment feature. The port is configured to be in fluid communication with an implantable band. The port comprises a septum operable to be pierced by a needle. The catheter is configured to establish fluid communication between the port and the implantable band. The catheter is further configured to deliver fluid to the implantable band. The sleeve is configured to interface with the port. The alignment feature is responsive to the catheter being fully secured to the port. The alignment feature prevents the port from being fully sutured to tissue unless the catheter is fully secured to the port.

Abstract: A multi-layer odor barrier catheter tube for a fecal drainage catheter. The layers of the catheter tube include one or more thermoplastic elastomer layers and one or more odor barrier layers. For example, the catheter tube may comprise an inner thermoplastic elastomer (TPE) layer, an intermediate odor barrier film layer, and an outer TPE layer. Alternately, the multi-layer catheter tube includes an inner TPE layer sandwiched between outer layers of odor barrier film material.

Abstract: A visually-coordinated absorbent product includes an absorbent article component including a garment side outer cover and a body side liner, wherein the article component has at least a first and second visual characteristic, and wherein the first visual characteristic is different from the second visual characteristic. The absorbent product also includes a first packaging component including at least first and second visual characteristics, wherein first and second visual characteristics of the absorbent article are coordinated to the first and second visual characteristics of the packaging component, and wherein at least a portion of one of the garment side outer cover and the body side liner is configured with the article component first visual characteristic and at least a portion of one of the garment side outer cover and the body side liner is configured with the article component second visual characteristic.

Abstract: A disposable absorbent article for receiving urine from an individual and a method of using the same are described. The absorbent article can include an absorbent body folded substantially longitudinally. The absorbent body can include a left-side portion and a right-side portion on opposite sides of the fold, and a proximal edge extending generally orthogonal to the fold. An interior receiving cavity can be defined by the left-side portion and the right-side portion of the folded absorbent body. The absorbent article also includes a penile opening defined by a portion of the proximal edge, where the penile opening is adapted for receiving a penis of a user into the interior receiving cavity. The absorbent body can include a liquid impermeable, exterior layer; a liquid permeable, fluid management layer; and an absorbent layer disposed between said exterior layer and said fluid management layer.

Abstract: A reusable outer cover is provided. The reusable outer cover is configured for use with a disposable absorbent insert to together form a wearable absorbent article. The reusable outer cover may be configured as a pull-on pant and may include a front waist region, a rear waist region, a crotch region disposed intermediate the front waist region and the rear waist region, and a wearer-facing surface. The wearer-facing surface of the front waist region or the rear waist region may include an insert fastener component. The reusable outer cover may further include a grasping aid configured to assist in the application of the article onto a wearer. The grasping aid may be force-coupled to the insert fastener component or to a reduced elongation zone in the reusable outer cover.

Abstract: An external absorbent device and a method for absorbing bodily fluids are provided. The external absorbent device includes an external tampon portion movably affixed to a sanitary napkin portion. The external tampon portion can be properly positioned between the labia of the wearer, and the sanitary napkin portion can be affixed to or rest within the crotch portion of an undergarment.

Abstract: In order to inhibit thrombotic processes locally rather than systemically, higher levels of antithrombotic drugs in the deep veins of the legs than in the systemic circulation are obtained using devices and methods that provide venous cannulation in the dorsum of the foot of a patient while applying pressure to the foot proximal to the venous cannulation, potentially as far up the leg as the knee, in an amount sufficient to compress the superficial veins and divert the venous drainage in the deep venous system into the venous plexus.

Abstract: A rotational atherectomy device for abrading a stenotic lesion from a vessel of a patient comprises a flexible drive shaft which extends towards a distal end of the device, a distal fluid inflatable support element located at a distal end of the drive shaft and an abrasive element mounted to the drive shaft proximal to and spaced away from the distal fluid inflatable support element. Both the abrasive element and the distal fluid inflatable support element are rotatable together with the drive shaft and the drive shaft comprises a torque transmitting coil which defines a long lumen of the drive shaft.

Abstract: Embodiments of a system including a remotely controlled reaction device and associated controller are described. Methods of use and control of the device are also disclosed. According to various embodiments, a reaction device is placed in an environment in order to perform a chemical reaction in an environment. Exemplary environments include a body of an organism, a body of water, or an enclosed volume of a fluid. In selected embodiments, an acoustic control signal may be used.