Abstract: The invention is a bicycle trainer to which a standard bicycle temporarily attaches for exercise and simulated rides. A lifting mechanism raises and lowers the front tire, and in preferred embodiments, a frame engages the rear tire to hold the rear tire in an elevated position against a resistance cylinder. The trainer includes support arms that connect to the bicycle and pivot the bicycle in an arcuate path back and forth in relation to a resistance cylinder. The resistance cylinder can thereby vary resistance against back tire revolution.

Abstract: A training dummy assembly includes a base, a column, a tensioning mechanism, a dummy. The base rests on the ground. The column is pivotally coupled to the base. The tensioning mechanism resiliently couples the base to the column. The dummy has a shape of a torso with head and is formed out of foam with an outer latex skin. The torso of the dummy is mechanically coupled to the column.

Abstract: The invention generally relates to exercise equipment that includes a pulley and cable mechanism. More specifically, the invention relates to an adjustable mounting device for the pulley so that the pulley may be mounted at different locations on the exercise equipment. This provides the user of such exercise equipment with the ability to adjust and readily fine-tune the position of the pulleys for proper biomechanical alignment with the user's body. Such a mounted pulley may be used on Pilates apparatus, weight and strength training equipment or other exercise equipment.

Abstract: A mechanical device is used for mounting and/or dismounting a laser nozzle on and/or from a nozzle mount of a laser processing machine for processing workpieces, especially metal sheets. The mechanical device includes a nozzle magazine having a nozzle holder support on which a nozzle holder for a laser nozzle is supported. In addition, the mechanical device has a support positioning drive by means of which the nozzle holder support is positionable together with the nozzle holder in a support positioning direction. A lifting device of the mechanical device serves to position the nozzle holder, when positioned in the support positioning direction in a lifting stand-by position, relative to the nozzle holder support in a positioning lifting direction extending perpendicular to the support positioning direction.

Abstract: A machine is disclosed for securing a closure system onto a discrete pouch. The machine includes first, second and third stations. The first station is capable of advancing discrete pouches and lifting and folding a portion of a first major surface of each pouch upon itself to form a lip, and exposing an inner surface of a second major surface. The second station is capable of positioning and attaching a closure system transversely across the exposed inner surface. The closure system includes a track having first and second legs each having an outer surface. The first and second legs are joined together by an opening/closing mechanism which includes a movable member capable of being moved back and forth. The third station is located downstream from the second station and is capable of unfolding the lip and securing opposite ends of the lip to the outer surface of the second leg.

Abstract: A method of manufacturing a top sheet material or back sheet material for use in the manufacture of disposable absorbent articles including the steps of: a) splitting a continuous first web of sheet material having substantially straight side edges into a second and third continuous web by an alternating concave-convex cutting line cut in a longitudinal direction along the continuous first web, the cutting line being distanced from both side edges of the continuous first web; b) shifting the second continuous web in a lateral direction in relation to the third continuous web so that the substantially straight edges of the second and third continuous webs are parallel to and adjacent to each other and longitudinally shifting the second continuous web so that the series of concave edge portions and the series of convex edge portions of the second and third continuous webs are longitudinally aligned with each other; c) directly or indirectly joining the substantially straight edges of the second and third contin

Abstract: Blanks used in the manufacture of nappies/diapers are folded on a machine comprising a first aspirating roller (5) by which single blanks (2) are advanced in succession toward a second aspirating roller (6) rotating counter and substantially tangential to the first roller (5) at a folding station (T).

Abstract: A medical unit includes a shielded enclosure (2) in which are accommodated:—elements (13) for supporting a container (12) including a source or a generator of injectable radioactive product (11),—elements (10) for supporting a syringe (6),—a device (3) of the activimeter type, and—a system of pipes (9, 20, 23, 24) associated with at least one valve (15). The syringe support (10), the valve (15) and the radioactive source support (13) are arranged vertically relative to one another, respectively from top to bottom, the syringe support (10) being arranged to support the syringe (6) with the plunger (8) thereof oriented upward. The valve (15) and the syringe plunger (8) can be operated so as to ensure the withdrawal, dilution and injection operations.

Abstract: An apparatus and method for micro-exercise apply piezoelectric stress to cells of a bone mass by inducing voltages in the bone mass. Application of dynamic, electromagnetic fields passing through the conductive bone mass induce currents and voltages locally in and around cells or groups of cells. The cells respond to the combination of mechanical stress and strain by building themselves up as they would if they had been subjected to the stress and strain of conventional exercise. Thus, micro-exercise at a cellular level of the bone mass can be stimulated as if the stress and strain had been applied to the entire bone structure of which the smaller cellular portions are constituent parts. In combination with casts or splints, the sources of electromagnetic flux may be embedded in the frame or solid structure, the protective padding added for comfort, or both.

Abstract: The device and method for reducing heart wall stress. The device can be one which reduces wall stress throughout the cardiac cycle or only a portion of the cardiac cycle. The device can be configured to begin to engage, to reduce wall stress during diastolic filling, or begin to engage to reduce wall stress during systolic contraction. Furthermore, the device can be configured to include at least two elements, one of which engages full cycle and the other which engages only during a portion of the cardiac cycle.

Abstract: An apparatus for inducing sleep includes an audio generator, a signal generator, and a signal processor. The audio generator generates audio signals. The signal generator generates electrical signals with a frequency between 0.4 HZ to 4 HZ. The signal processor adjusts amplitudes of the audio signals according to the frequency, and outputs the adjusted audio signals.

Abstract: A device for treating fecal incontinence in a subject is provided. The device includes a plug configured for positioning mostly within an anal canal of the subject.

Abstract: The invention, in various embodiments, is directed to systems, devices, and methods relating to pre-pubic approaches to delivering a supportive sling to periurethral tissue of a patient.

Abstract: The present invention relates to a system for the central control of devices used during an operation, comprising a first control unit for control of said devices. The system is characterized in that a second control unit is provided which is connected to the first control unit for exchange of information. The first control unit may be embodied as closed system for control of at least those devices which carry out safety-related functions (safety-related devices), and the second control unit may be embodied as open system for control of the remaining devices which carry out non safety-related functions (non safety-related devices). The invention further relates to a method for the central control of devices.

Abstract: A capsule endoscope includes a capsule-shaped casing and an imaging unit for taking an image of an inside of an organ in a state where the capsule endoscope is floating in liquid introduced inside the organ of a subject. Specific gravity of the capsule endoscope to the introduced liquid is ?; a plane divides the capsule endoscope such that a volume ratio is to be ?:1??. A straight line that connects a center of volume of a portion whose volume ratio is ? and a center of gravity of the capsule endoscope is substantially perpendicular to the plane. The center of gravity is present at a position farther distant from the plane than the center of volume. A surface of a boundary of a field of view that forms an angle of view of the imaging unit and the plane do not intersect outside the capsule endoscope.

Abstract: An imaging mode is automatically switched based on the kind of a subject. The spatial frequency of an endoscopic image obtained by imaging the subject is detected. Further, judgment is made, based on the distribution of the spatial frequency, as to whether the endoscopic image was obtained by performing close-up imaging on the subject. The condition of imaging is switched based on the result of judgment as to whether the image was obtained by close-up imaging or distant-view imaging.

Abstract: Apparatus and methods for locating morphological features within a body cavity using a catheter including proximal and distal ends, a transparent balloon carried on the distal end, and an optical imaging assembly carried on the distal end for imaging through the balloon. The balloon includes a channel extending therethrough to a lumen extending through the catheter. A guidewire or other localization member is received in the lumen that is extendable through the channel. During use, the catheter is inserted into a right atrium of a heart, and the balloon is expanded and placed against the wall of the heart to locate the coronary sinus. Sufficient force is applied to clear blood between the surface and the wall and clear the field of view of the imaging assembly. The catheter is manipulated to locate the coronary sinus, whereupon the localization member is advanced into the coronary sinus.

Abstract: The present invention provides a balloon controller for an endoscope apparatus having a fluid supply and drawing device which communicates with at least one of a balloon attached to an insertion portion of an endoscope and a balloon attached to an insertion assist implement for guiding the insertion portion when the insertion portion is inserted, and which supplies a fluid to each balloon or draws the fluid from the balloon, the balloon controller comprising: a leakage device provided in tube paths for communication between the balloons and the fluid supply and drawing device, the leakage device being capable of leaking the fluid.

Abstract: A medical instrument including a distortion detection probe disposed in an insertion portion to be inserted into the interior of an examinee provided with a plurality of FBG sensor sections that detect distortion of the insertion portion, a coordinate calculation section that calculates first three-dimensional coordinates of the respective FBG sensor sections according to a first three-dimensional coordinate system whose origin is a predetermined position based on the detection results of the FBG sensor sections, a coordinate system setting section that sets a second three-dimensional coordinate system based on the first three-dimensional coordinates of the respective FBG sensor sections, a coordinate transformation section that transforms the first three-dimensional coordinates of the respective FBG sensor sections into second three-dimensional coordinates according to the second three-dimensional coordinate system set by the coordinate system setting section and a shape display section that displays the sha

Abstract: In an endoscope, a solid-state image pickup device images an object, to output an image signal. In a processing apparatus, an illuminator applies normal light and specific light having spectral distribution different from the normal light to the object. A display control unit operates according to the image signal, to cause display of a normal image of the object produced by applying the normal light, and a specific image of the object produced by applying the specific light. A motion detector detects information of relative motion of the object. A controller controls the illuminator, causes alternate emission of the normal and specific light periodically at a storage period of the image pickup device if the motion information is equal to or smaller than a threshold level, and causes emission of the normal light without emitting the specific light if the motion information is greater than the threshold level.

Abstract: In a treatment endoscope which includes: an elongated insertion section having a first channel for inserting a treatment instrument therethrough; an arm, having a second channel for inserting a treatment instrument therethrough, attached to the distal end of the insertion section so that the first channel communicates with the second channel; a first operation section for operating the arm; and a second operation section for operating the insertion section, the arm has a first bending section which can be operated to be bent via the first operation section, the insertion section has a second bending section which can be operated to be bent via the second operation section, and an interlock mechanism connects the first operation section to the second operation section so that, when either one of the first bending section and the second bending section is bent by operating either one of the first operation section and the second operation section, the other one of the first bending section and the second bendin

Abstract: An endoscope includes, an insertion section, a distal end section body has an observation window, a liquid feed path which is formed to supply a liquid to the distal end section body side, a gas feed path which is formed to supply a gas to the distal end section body side, and a nozzle having a confluent portion which makes confluent the liquid supplied from the liquid feed path and the gas supplied from the gas feed path, and a jet outlet which jets a gas/liquid mixture fluid, which is mixed in the confluent portion, toward the observation window, wherein the nozzle is configured such that an angle, which is formed between a direction of a flow of the liquid toward the jet outlet and a direction of a flow of the gas toward the jet outlet, is set at an obtuse angle of 90° or more.

Abstract: A cannula assembly includes a tubular element forming a lumen, a deployable portion of the tubular element, and an electronic component mounted to the deployable portion of the tubular element. The tubular element has a proximal end and a distal end adapted to be inserted into a body cavity. The deployable portion of the tubular element is engaged near the distal end of the tubular element so as to transition between a closed position and an open position. The electronic component is at least partially disposed in the lumen when the deployable portion is in the closed position.

Abstract: Laparoscopic instruments and cannulas are provided for performing laparoscopic procedures entirely through the umbilicus. Generally S-shaped laparoscopic instruments placed through the C-shaped trocar sleeves or through the cannula and instrument holder unit provide markedly improved degrees of instruments' freedom during trans-umbilical laparoscopic procedures.

Abstract: A surgical access system including a tissue distraction assembly and a tissue refraction assembly, both of which may be equipped with one or more electrodes for use in detecting the existence of (and optionally the distance and/or direction to) neural structures before, during, and after the establishment of an operative corridor to a surgical target site.

Abstract: A ring for dilating a pupil during an ophthalmic procedure includes a series of spaced supports for engaging an iris perimeter. The supports are plate elements which form an open pocket directed outwardly for engaging the iris. The sides of the ring form a primary plane, and the plates are located in respective planes above and below the primary plane. The outer periphery of the top and bottom plates forms a lip feature which is the opening to the pocket which retains the iris.

Abstract: A portable medical system is provided for the purposes of analysis and/or medication, the system having at least one of a medical monitoring device, an analysis device and a medication device. The portable medical system comprises at least one display element comprising at least one organic light-emitting diode display. An optimization device can be provided that comprises a brightness sensor and is configured to optimize the brightness, contrast and/or power consumption of the at least one display element. Furthermore, a monitoring device can be provided which monitors the functionality of the display element. Faults in the display element can be detected in this way, and a corresponding warning can be output to a person using the portable medical system.

Abstract: Embodiments of systems and methods for providing protocols for administering an aspect of care are presented. Specifically, certain embodiments relate to a sepsis diagnosis and management protocol which may have been segmented according to the severity of the sepsis, where the care directives provided by the differing segments of the protocol will be of differing intensity or invasiveness based upon the severity of the patient's disease. Embodiments of such protocols may be implemented in conjunction with computer systems to aid in providing that aspect of care in conjunction with a particular patient.

Abstract: The invention relates to a method and an apparatus for monitoring the autonomous nervous system of a sedated patient. According to the method, skin conductance is measured through a time interval. Average skin conductance values and the number of fluctuation peaks are in the interval are calculated and analyzed, and an indication is given of the state of pain/discomfort in the patient as well as the state of awakening in the patient. The invention is particularly applicable for use with anaesthetized or artificially ventilated patents, as separate output signals are automatically provided, indicating the need for analgesics and hypnotics, respectively.

Abstract: The present invention is directed to a method of reducing false readings in a hypoglycemic detector that includes establishing a predetermined hypoglycemic threshold, a predetermined critical threshold, a predetermined rate of change in glucose concentration where the predetermined critical threshold is below the predetermined hypoglycemic threshold. A first sampling rate is then calculated based upon said predetermined hypoglycemic threshold, said predetermined critical threshold, and said predetermined rate of change in glucose concentration.

Abstract: The invention relates to an inserter for a transcutaneous sensor comprising a sensor part e.g. for registration of the bloods content of glucose. The inserter comprises a needle unit comprising a needle hub and a carrier body, and a sensor housing. The sensor housing and the needle hub are releasably connected and when they are connected, the insertion needle is placed along the sensor e.g. surrounding the sensor wholly or partly. The carrier body guides the movement relative to the housing between a retracted and an advanced position. When released the needle unit and the sensor housing are forced by a spring unit to an advanced position where the needle and sensor are placed subcutaneously. The object of the invention is to provide a disposable inserter for a transcutaneous sensor which inserter is easy and safe for the user to handle during use and to dispose of after use.

Abstract: An ultrasonic diagnostic apparatus includes a structure for adjusting the positional relationship between an ultrasonic transducer and a blood vessel for measuring an elasticity characteristic. The apparatus includes an ultrasonic probe including a transducer for transmitting an ultrasonic wave and receiving the ultrasonic wave reflected by a tissue of a biological body; and a driving device for physically moving the transducer. For measuring the elasticity characteristic of the blood vessel, the driving device moves the transducer based on a control signal to change at least one of a direction and a position at which the ultrasonic wave is to be transmitted. A determination section specifies a position of the transducer at which the reflection intensity is maximum based on intensity information representing an intensity of the reflected wave. A calculation section calculates the elasticity characteristic of the blood vessel at the specified position.

Abstract: Adjustment of operation of an ultrasound imaging system may be based at least in part on one or more characteristics represented in ultrasound return signals from two or more sample volumes. Adjustment may include adjusting a principal sample volume location or selecting a new principal sample volume. For example, a location of a principal sample volume may be adjusted or new principal sample volume selected so as to remain focused on an identified region of interest or to maintain the principal sample volume relative to some structure or reference. The principal sample volume may be maintained in the center or along a centerline of an artery or other structure, as the transducer array is moved along the artery or structure.

Abstract: A method of measuring the thickness of a biological tissue by ultrasounds and a device carrying out such method. The method is implemented with an ultrasound probe that emits ultrasonic pulses within a body under examination and receives echoes generated from structures of the body under examination. The probe includes an array of two or more electro-acoustic transducers and, in combination, means for processing the reception signals and means for orienting one or more lines of sight, along which the emission of the pulses and/or the reception of the echoes is focused, according to different angles with respect to an axis perpendicular to the emitting surface of the probe.

Abstract: A method of operating an ultrasound signal generator includes generating a stimulus signal and receiving a returned signal. The Signal to Noise Ratio (SNR) of the returned signal is computed. The SNR is compared to an optimal SNR range. A control signal is generated to control the transmission power of the stimulus signal. A new stimulus signal is generated at the new transmission power. A device for collecting and analyzing a quasi-periodic signal includes a SNR calculator that computes the SNR of a returned signal. A signal analysis selector selects between a first and a second signal analysis technique. A transmission power controller compares the computed SNR with an optimal SNR range for the selected technique and modifies the transmission power as a result of this comparison.

Abstract: An ABPI measurement system includes two cuffs for each ankle and two cuffs for each arm of a patient. Each cuff has chambers. The four cuffs are applied to each limb (or finger or toe), each chamber is inflated simultaneously to a pressure until a Pneumo Arterial Plethysmography (PAPG) signal related to the arterial flow in the limb is detected at the chambers. The chambers are then simultaneously inflated until the PAPG signals are extinguished in each limb, the inflation of chambers continuing for 10 mmHg to 20 mmHg above that pressure. The chambers are then deflated and the pressure at which the PAPG signal returns in the first chamber is recorded for each limb and this value of the pressure is used to calculate the ABPI. The ABPI is displayed or sent to a remote site.

Abstract: A step rate optimization device (12). The device includes a timer, a pedometer, an arterial waveform sensor (24), a processor and an indicator (16). The device indicates to the user (10) of a substantially sub-optimal relationship between the user's pulse rate and stride rate when the user's dominant stride rate frequency is at about 2-3 Hz and has a larger amplitude than the component of the user's dominant pulse waveform frequency at about 4-7 Hz and of a substantially optimal relationship between the user's pulse rate and stride rate when the user's dominant stride rate frequency component is at about 4-7 Hz and has a larger amplitude than the component of the user's dominant pulse waveform frequency at about 2-3 Hz.

Abstract: A system and method is disclosed for measuring muscle reflexes (e.g., a bulbocavernosus reflex) as a tool for identifying/diagnosing dysfunctions (e.g., spinal cord abnormalities, bladder voiding dysfunction, and sexual organ dysfunction) non-invasively by using mechanical stimulation. The system and method includes a probe having a predetermined patient contacting portion, wherein when the contacting portion is moved into contact with a particular area of the patient (e.g., the patient's genitals), the contact induces a muscle reflex. The probe detects the pressure resulting from the contacting portion being abruptly and forcibly brought into contact with the particular area. Such detection is used to electronically initiate capture of electrical responses from a plurality of electrodes placed on the patient's skin in proximity to the particular area. Such electrical responses are processed to determine characteristics of the patient's reflexes of one or more muscles adjacent to the electrodes.

Abstract: A bone biopsy device includes an outer cannula having a mouth with a cutting edge to section a frustule of spongy bone, a plate mounted slidably within the cannula and provided with a semi-cylindrical portion at its distal end, and a stylet mounted slidably within the plate and provided with a pointed tip which protrudes from the mouth of the cannula to pierce the compact part of the bone. The mouth of the cannula has on its inside a narrowing and the semi-cylindrical part of the plate has at its distal end at least one pair of opposed circumferential sets of teeth adapted to bend radially inwards when they encounter the narrowing of the mouth, to clasp the base of the sectioned frustule and allow extraction of the frustule by the plate while the cannula is kept at the operating site, allowing aspiration of marrow after the frustule has been removed.

Abstract: A combination exo-endocervical sampling device includes a shaft that includes a first end opposite a second end, and a combination exo-endocervical sampler configured to simultaneously collect endocervical cells and exocervical cells. The combination exo-endocervical sampler is coupled to the second end and includes a pair of opposing wings disposed transverse to the shaft and a brush extending from the wings along a central axis of the shaft. Each of the opposing wings includes a plurality of flexible loops configured to collect exocervical cells.

Abstract: A blood testing device that can perform blood testing having lighting intensity independent of the number of times of piercing. The blood testing device (21) has a cover unit (20) removably installed on negative pressure chambers (25a, 25b). The cover unit (20) has a circular tube section (20b) surrounding the optical axis of a laser unit (26) and having a predetermined length in the direction of the optical axis, a cover glass (20d) placed on the optical axis of the laser unit (26) so as to be located at that end of the circular tube section (20b) which is on the laser unit (26) side, and a slit (20e) for interconnecting the inside of the circular tube section (20b) and the negative pressure chamber (25a) outside the circular tube section (20b).

Abstract: An intestinal peristalsis detecting device comprises a radio frequency (RF) signal generator, an antenna, and a mixer. After the RF signal generator sends a pulse signal, the antenna receives the pulse signal and emits a pulse electromagnetic wave to an organism. Thereafter, the antenna receives a response pulse electromagnetic wave reflected from the organism to generate a response pulse signal. The mixer couples with the RF signal generator and the antenna to mix the pulse signal and the response pulse signal.

Abstract: This disclosure relates to cervical sizing devices and related kits and methods. In some aspects, a cervical sizing device includes an elongate arm and a member positioned at a distal end region of the elongate arm. The cervical sizing device can be used to determine an approximate size of a cervix when the member is brought into contact with an outer surface of the cervix.

Abstract: A lumen passability checking device includes: an expandable and shrinkable outer casing that contains a predetermined fluid, is expanded by a pressure of the contained fluid, and forms an external diameter substantially equal to that of a capsule medical device to be inserted into a body of a subject; and a shape manipulating unit that flows out the fluid contained in the outer casing to shrink-deform the outer casing. The outer casing is shrink-deformed by flowing out the fluid, while maintaining a state of being integrated with the shape manipulating unit.

Abstract: A walk assistance device comprises a thigh unit configured to be arranged on a thigh of the user, a shank unit configured to be arranged on a shank of the user, a foot unit configured to be arranged on a foot of the user, a knee position joint unit configured to couple the thigh unit and the shank unit in a swingable manner, and an ankle position joint unit configured to couple the shank unit and the foot unit in a swingable manner. The shank unit comprises a first replaceable member and a second replaceable member that extend along the shank of the user, and a length of the shank unit is adjustable by replacing each of the first and second replaceable members with another one having a different length.

Abstract: An electric moxibustion device includes a tubular case having a front end opening, a heater unit placed near the front end opening in the case, and a heatproof rubber cap removably attached to the front end of the case. The heater unit comprises a heat transfer metal plate and a heating element which is fixed on the back surface of the heat transfer metal plate and generates heat using power from an external power source or a battery. The cap and the case are configured for holding an absorbent-retentive member which absorbs and retains a medical fluid between the discharge opening of the cap and the heat transfer metal plate in the case. The case has a thermoregulation circuit built-in which can change the temperature of the heating element in a stepwise manner, and push buttons for temperature adjustment are provided on the outer periphery of the case.

Abstract: An ankle therapy device provides variable loading on targeted muscles and tendons, by utilizing a variable length moment arm to which the load is attached, and having the ability to change the angle of the load with respect to the orientation of the user's foot. Thus, the device provides a variable resistance on the ankle muscles and tendons when the ankle is moved, and may target different muscles and tendons by changing the angle of the resistance. The device comprises a member to which the user's foot is attached, and a rotatably attached weight support member to which a weight is secured. The position of the weight may be shifted along the length of the weight support member, and the amount of weight may be changed.

Abstract: A massaging device in the shape of a rod with an essentially cylindrical end element with a sleeve. The device has a flexible sleeve and a drive element to produce an oscillating deformation of the sleeve.

Abstract: A walking cast having an upper cage assembleable over an upper leg and a lower cage assembleable over a lower leg and hingedly secured to the upper cage approximate a wearer's knee. A foot sole support is connected to the lower cage which includes lower angled supports for engaging side locations of the sole in a further hinged connection. Each of the upper and lower cages include a rear positioned fixed support with a second forward and hingedly connecting door. A plurality of cushioning supports secure to inner facing locations associated with each of the upper and lower cages.

Abstract: A method and a device for recognition of paravasal bleeding upon a supplying of blood to a vascular access via a line and/or upon the removal of blood from a vascular access via a line is provided. A device for extracorporeal blood treatment comprising a device for recognition of paravasal bleeding is also provided. The method and the device are based on the change of arterial pressure in the arterial branch or the venous pressure in the venous branch of the extra-corporeal circuit being registered during the extracorporeal blood treatment. One aspect of the method and the device is that pressure changes that come from a pressure level exhibiting a large difference from a reference value are more strongly considered than those that come from a pressure level that exhibits only a minor difference from the reference value.