Abstract: The invention relates to a guide device (1), in particular for positioning catheters in a body duct. The guide device (1) has an extended first thread (2) and at least one extended second thread (3) made from wire, which runs close to the first thread (2). According to the invention, the guide device (1) has a device (8), provided for one of the threads (2, 3) by means of which it is possible to actively control a relative movement between the threads (2, 3) or at least make the same difficult. The control device (8) is for example embodied such that the first thread (2), prepared from a flexible material, exerts a pressure, preferably acting a radial direction, on the several second threads, or that magnetic fields (4) of differing polarities along the first thread (2), prepared from a flexible material and along the second thread (3), may be generated for the selective introduction of an opposing attraction of the threads (2, 3) for reinforcing the guide device (1).

Abstract: A system for measuring the size of a gastric lumen includes a gastric banding device, an antenna positioned outside of the patient's body, and a receiver in operative communication with the antenna. The banding device comprises two orthogonal ultrasonic transceiver modules, a microprocessor, and a transmitter in electrical communication with the microprocessor. The microprocessor is in operative communication with each of the two transceiver modules. The transmitter transmits signals to a receiver positioned outside of a patient's body. Another system for measuring the size of a gastric lumen includes a gastric banding device having a first coiled conductor. The system further comprises a circuit external to the banding device, the circuit comprising a second coiled conductor. The circuit further comprises a tunable frequency generator and a spectrum analyzer, the circuit being tunable to allow a resonant frequency.

Abstract: Systems for and methods of assessing urinary flow rate via sound analysis. Embodiments of the uroflow measurement systems include a computer and a telephone or a digital recording mechanism to capture the sound of one or more urination events, which are stored as audio files in a database. The uroflow measurement systems may include sound analysis software for analyzing the strength and duration of each urination event and may include a web-based uroflow software application for viewing the results via the Internet or other network. In one embodiment, the sound analysis software performs the steps of reading in the raw data of a selected audio file, generating a plot of the audio signal amplitude vs.

Abstract: A fluid handling module that is removably engageable with a bodily fluid analyzer is provided. The module may comprise a fluid handling element, and a fluid component separator that is accessible via the fluid handling element and configured to separate at least one component of a bodily fluid transported to the fluid component separator. The fluid handling element may have at least one control element interface.

Abstract: A biopsy device targeting set includes a vertical member, a carriage that is vertically movable along the vertical member, and a cradle coupled with the carriage. The cradle has a pair of substantially perpendicular mounting arms. Each mounting arm has a recess that may receive a rail of the carriage, such that the cradle may be mounted to the same rail in different orientations. Each mounting arm also has a biopsy device mounting feature, which may be a recess or a rail. The biopsy device mounting feature is configured to engage with a complementary feature of a biopsy device, such that a biopsy device may be mounted to either mounting arm. A z-stop feature is operable to selectively restrict longitudinal motion along either or both of the biopsy device mounting features. The targeting set may be used with a biopsy device in an MRI environment.

Abstract: A system for at least partially filling and marking a cavity at a site within a patient's body includes a marker delivery device having a chamber configured to contain a marking substance and having a mechanism configured to expel the marking substance. A quantity of the marking substance is contained within the chamber of the marker delivery device. The marking substance is configured to at least partially fill the cavity and form therein a porous bioabsorbable body. A delivery tube is coupled in fluid communication with the chamber of the marker delivery device. The delivery tube has a distal end with a discharge port through which the marking substance is expelled. A releasable remotely detectable distal tip is coupled to the distal end of the delivery tube and is configured to be released to remain within the porous bioabsorbable body within the cavity upon the formation thereof.

Abstract: A catheter has a control handle with at least an outer thumb control and an inner second thumb control. A longer puller wire has a distal end anchored at or near a distal end of distal deflectable portion. A shorter puller wire has a distal end anchored at or near a distal end of the proximal deflectable portion. For the shorter puller wire, a shorter compression coil has a distal end at or near a proximal end of the intermediate deflectable section. For the longer puller wire, a longer compression coil has a distal end at or near a distal end of the shorter puller wire. The inner and outer thumb controls include engagement members releasable by rotation of one thumb control relative to the other. When disengaged, the thumb controls each can be moved longitudinally relative to each other. When engaged, the thumb controls are coupled together for longitudinal movement as a single unit relative to the control handle.

Abstract: Apparatus for performing impedance measurements on a subject. The apparatus includes a first processing system for determining an impedance measurement procedure and determining instructions corresponding to the measurement procedure. A second processing system is provided for receiving the instructions, using the instructions to generate control signals, with the control signals being used to apply one or more signals to the subject. The second processing system then receives first data indicative of the one or more signals applied to the subject, second data indicative of one or more signals measured across the subject and performs at least preliminary processing of the first and second data to thereby allow impedance values to be determined.

Abstract: Methods and instruments for assessing bone, for example fracture risk, in a subject in which a test probe is inserted through the skin of the subject so that the test probe contacts the subject's bone and the resistance of the test bone to microscopic fracture by the test probe is determined. Macroscopic bone fracture risk is assessed by measuring the resistance of the bone to microscopic fractures caused by the test probe. The microscopic fractures are so small that they pose negligible health risks. The instrument may also be useful in characterizing other materials, especially if it is necessary to penetrate a layer to get to the material to be characterized.

Abstract: A method for hair cell stimulation includes determining a frequency band corresponding to damaged hair cell region in accordance with a preset algorithm, determining the frequency band corresponding to the damaged hair cell region as a target frequency band, and outputting an acoustic signal with given intensity to the target frequency band so as to stimulate the damaged hair cell region. The method treats hearing loss by acoustic signal.

Abstract: An apparatus and method for analyzing an analyte in a body fluid sample using a lancing device (10) having a hollow lancet are disclosed. According to one embodiment of the present invention, the method comprises the acts of lancing the skin of a test subject with the hollow lancet (18) having an interior of the hollow lancet (18) that forms a capillary channel, collecting a body fluid sample from the lanced skin in the capillary channel of the hollow lancet (18), and analyzing the body fluid sample for determining the analyte concentration in the body fluid sample while the collected body fluid sample remains in the lancet (18).

Abstract: The present invention provides a evaluating system of masticatory efficiency comprising a first step of allowing a human subject to masticate an artificial food material containing microparticles that are finely crushed and ground by mastication and keep a spherical shape unless they are masticated; a second step of enlarging the artificial food material having been thus masticated by applying pressure to a thickness equal to the diameter of the microparticles while sandwiching the artificial food material between two preparation sheets; and a third step of counting microparticles keeping the spherical shape that remain in the artificial food material having been enlarged between the two preparation sheets by applying pressure. By using this evaluating system in the invention, the masticatory efficiency can be evaluated well in precise and at short time without using a solvent and expensive instruments.

Abstract: A sensor for sensing bioacoustic energy includes a housing comprising an interfacing portion configured to establish coupling with a body part during use. The sensor includes a transducer element coupled to the interfacing portion of the housing and configured to sense sounds produced by matter of biological origin. One or more conductors are coupled to the transducer element. A mass element is compliantly coupled to a surface of the transducer element. Intervening material is disposed between the transducer element surface and the mass element, and allows for differential motion between the transducer element surface and the mass element during excitation of the transducer element.

Abstract: A test unit cartridge for holding a plurality of test units includes a first test unit that contains a first analyte sensor and a second test unit that contains a second analyte sensor. The first and second analyte sensors use first and second reagents to detect first and second analytes, respectively. The first analyte is different from the second analyte and the first and second test units are functionally non-fungible. The plurality of test units can also include a third test unit that contains two analyte sensors having two reagents for detecting two different analytes using one fluid sample. A method of using the test unit cartridge is also described, which comprises loading the cartridge into an analyte testing device and cocking an actuator of the device that is configured to (i) expose an analyte sensor of a test unit, (ii) ready a lancet, and (iii) advance a lancet cartridge.

Abstract: A test unit cartridge for holding a plurality of test units includes a first test unit that contains a first analyte sensor and a second test unit that contains a second analyte sensor. The first and second analyte sensors use first and second reagents to detect first and second analytes, respectively. The first analyte is different from the second analyte and the first and second test units are functionally non-fungible. The plurality of test units can also include a third test unit that contains two analyte sensors having two reagents for detecting two different analytes using one fluid sample. A method of using the test unit cartridge is also described, which comprises loading the cartridge into an analyte testing device and cocking an actuator of the device that is configured to (i) expose an analyte sensor of a test unit, (ii) ready a lancet, and (iii) advance a lancet cartridge.

Abstract: An integrated lancing test strip device includes a lancet configured to form an incision in tissue and a test strip coupled to the lancet for analyzing body fluid. A retention mechanism acts as a detent to hold the lancet in a static position relative to the test strip before forming the incision. The retention mechanism is configured to release the lancet for retracting the lancet relative to the test strip to reduce smearing of body fluid by the lancet during collection of the fluid with the test strip. In one form, the retention mechanism includes breakable tabs that are broken to release the lancet, and the lancet is retracted via translational movement. The retention mechanism in another form includes one or more dimples that release the lancet when the lancet is retracted via rotational motion. In a further form, the entire integrated device is rotated to collect fluid.

Abstract: Real-time monitoring of tissue ablation is possible by using a vibrating ablation needle coupling lateral shear waves to the tissue. Ultrasonic imaging may characterize the velocity of these shear waves to reveal Young's modulus of the tissue and, at a discontinuity in Young's modulus, a boundary of the ablated lesion reflecting an underlying increase in stiffness of ablated tissue. This technique may be coupled with quasi-static elastography-based ablation monitoring techniques for improved measurement.

Abstract: A measuring device for measuring a depth of a tear of a tissue is disclosed. The measuring device comprises a member having a shaft and a distal tip, a plurality of indicia on the shaft of the member for measuring the depth of the tear, and a cannulated member into which the member is disposed. In an example, the measuring device is used to measure the depth of a tear of the rotator cuff tendon. A method of measuring a tear of a tissue using the measuring device is also disclosed.

Abstract: A first trocar as an medical apparatus includes an insertion hole having a projection opening for leading out a biopsy forceps into a body of a subject, a lid body for blocking the projection opening of the insertion hole, and a cooling sheet for cryogenically cooling a biopsy portion arranged in the vicinity of the lid body in a state where the biopsy forceps is stored in the insertion hole, and is capable of easily harvesting a living tissue while retaining morphological change of tissues in a living body under various hemodynamics.

Abstract: This invention provides a guide wire whose structural features can be determined through an endoscope. The guide wire is inserted into a patient's body and used in the lumen. It has markings at the positions where the structural features change.