Abstract: This optical cosmetic device for bodily hair is provided with optical systems for illumination with cosmetic light for bodily hair. The value of the integral of the intensity of the cosmetic light for bodily hair in the 800 nm-1200 nm wavelength range is greater than that in the 400 nm-800 nm wavelength range. The value of the integral of the intensity of the cosmetic light for bodily hair in the 400 nm-850 nm wavelength range is less than that in the 850 nm-1200 nm wavelength range.

Abstract: A system that automatically detects a myocardial barotrauma (i.e., tissue pop) event so that proper post-procedure care can be given includes an electronic control unit (ECU), a computer-readable memory coupled with the ECU, and detection logic stored in the memory configured to be executed by the ECU. The detection logic is configured to receive a signal generated by an electro-acoustic transducer related to acoustic activity within the patient, monitor the signal for a pre-determined indication of a barotrauma event, and output a notification when the pre-determined indication is detected. The transducer can be integrated with an extra-body patch that includes one or more electrodes for use with a medical device navigation system.

Abstract: The invention relates to a cavity determination apparatus for determining a cavity (3) within an object (2), in particular, for determining the location and dimensions of a heart chamber within a person. A bendable segment of an introduction element (5) is arranged within the cavity in different arrangements, wherein curves defined by the bendable segment in the different arrangements are determined by a curve determination unit (7). A cavity reconstruction unit (8) reconstructs the cavity based on the determined curves. Thus, not only single locations within the cavity are acquired and used for reconstructing the cavity, but larger curves. A lot of spatial information can therefore be acquired and used very fast. This allows reconstructing the cavity with improved quality in a relatively short time.

Abstract: The present invention relates to systems and methods for characterizing at least one anatomical parameter of an upper airway of a patient by analysing spectral properties of an utterance, comprising: a mechanical coupler comprising means for restricting the jaw position of the patient; means for recording an utterance; and processing means for determining at least one anatomical parameter of the upper airway from the recorded utterance and comparing the recorded utterance to a threshold value. In addition the present invention relates to the use of the above mentioned systems as a diagnostics tool for assessing obstructive sleep apnea.

Abstract: The present invention in several embodiments is a mobility assessment device which is easy to use and which will aid practitioners in evaluating a patients' mobility. The mobility assessment device of the present invention is preferably constructed from a skid resistant high contrast material that can easily be folded, rolled or stored in a compact space. The mobility assessment device of the present invention may include markings or indicia to aid a patient in properly performing one or several mobility assessment tests. The included indicia may have measurements and other marking for aiding a medical professional in evaluating a patient's mobility.

Abstract: A fluid sampling ports for withdrawing and administering fluids from or to a sampling site. The sampling valve is interconnected in a line to and/or from a patient with the line carrying a fluid that one wishes to sample. In a particular example, the sampling valve or port is interconnected in an arterial line and/or serves as a dialysis fluid sampling port.

Abstract: Systems and methods are provided for in vivo measurement of pressure. An implantable sensor assembly includes a pressure sensor configured to provide an analog signal representing pressure and a signal conditioning component configured to convert the pressure sensor output into a digital signal. A transmitter is configured to transmit the digital signal to an external base unit. A power control unit is configured to dynamically allocate power throughout the implantable sensor assembly, such that during an active measurement interval of the implantable sensor assembly, each of the pressure sensor, the signal conditioning component, and the transmitter are powered only for a portion of the active measurement interval necessary to perform a related function.

Abstract: The device is used to measure bioimpedances and has in each case at least one measurement electrode for each foot and each hand of a person who is to be measured. The electrodes are connected to an evaluation unit. In addition, at least one balance is used to determine a body weight of the person who is to be measured. The hand electrodes, provided for contact with the hands of the person who is to be measured, are arranged in the area of at least one positionable support element.

Abstract: A muscle activity and skeletal monitoring system and method are disclosed. A network of at least two distributed inertial sensor nodes are configured to communicate with each other over a first interface. Each of the inertial sensor nodes comprises at least one sensor configured to sense muscle vibrations and monitor body motion. A muscle activity recognition and motion tracking and visualization methods also are disclosed.

Abstract: Techniques are described for improving results of hearing tests. For example, the hearing tests described herein may be divided into multiple hearing test segments which may be provided to the test subject individually. Additionally, the hearing test may include multiple cognitive test segments that may be interleaved between the hearing test segments to gauge the test subject's awareness level.

Abstract: A biopsy device includes an elongated probe having a central longitudinal axis, a proximal end, a distal end, and an aperture. A tissue penetrating tip includes a proximal base secured to the distal end of the probe. A sharp distal point distal to the proximal base lies on the central longitudinal axis. Each of a first, second and third concave surface is configured to extend from the base to the sharp distal point. The second concave surface is located to intersect the first concave surface to form a first curved cutting edge. A third concave surface is located to intersect the first concave surface to form a second curved cutting edge and is located to intersect the second concave surface to form a third curved cutting edge. Each curved cutting edge extends from the base to the sharp distal point. A tissue cutting device is coaxial with the probe.

Abstract: A patient treatment unit and method analyzes and treats pain in tissues by applying an electrical pulse train to the affected tissue. The impedance of the affected tissue is measured, and the measured impedance is correlated to a level of pain in the patient. The pulse train is further applied in response to the measured impedance to reduce the patient's pain. The patient treatment unit includes a probe stimulus generator that outputs the pulse train. The treatment unit also includes a pair of probes for contacting the patient's body and receiving the pulse train. The pulse has improved shaping based on isolation of high voltage from a low voltage control. The unit further includes a body impedance analysis circuit that senses voltage and current via the probes when the probes are contacting the patient and observe the impedance. A monitor is electrically coupled to the body impedance analysis circuit and provides an indication of the measured impedance indicative of the patient's level of pain in real-time.

Abstract: An example method for preparing a surgical site for a femtosecond laser-assisted cataract surgical procedure includes measuring a lower eyelid length of a patient, and determining whether the patient is associated with one or more exposure resistant factors. The method also includes, upon determining that the measured lower eyelid length does not exceeds a threshold length or determining that the patient is associated with at least one exposure resistant factor, performing a canthotomy procedure on the patient.

Abstract: An intraocular pressure measuring and/or monitoring system comprises an intraocular pressure measuring device (1) comprising a support (3) and a pressure sensor (2) united with the support. The support (3) is configured for placing the pressure sensor (2) in contact with an eye (8) of a user for sensing the intraocular pressure (IOP) of the eye. A portable recording device (6) is configured for communicating with the intraocular pressure measuring device (1) and for storing data received from the intraocular pressure measuring device. The system further comprises an inertial and/or environmental sensor (9).

Abstract: A male coupler for a guidewire, the guidewire having a hollow walled tube, the male coupler comprising a connector section, coupled with the guidewire, a portion of the connector section having a diameter smaller than the diameter of the hollow tube, at least one conducting ring coupled with the connector section where the diameter of the connector section is smaller the diameter of the guidewire, wherein the diameter of connector section and the at least one conducting ring substantially equals the diameter of the guidewire.

Abstract: The systems and methods described herein are directed to monitoring the force or pressure applied to a portion of the human body, including in the neck region of a patient during a medical procedure, such as tracheal intubation, to ensure that the medical personnel are applying the desired level of force, and in regions of bony prominences to monitor and prevent the formation of pressure ulcers or decubitus ulcers. In particular, the systems and methods described herein include piezoresistive elements connected to signal processing circuitry for measuring the force or pressure.

Abstract: A guide wire includes a core shaft, a coil body which covers the core shaft, and a coating film which covers the coil body. Portions of the coating film are disposed between adjacent coils of coil body, and gaps are formed between the coils and the portions of the coating film disposed between the adjacent coils. Due to this configuration, the coating the film can be easily bent, and thus the coil body may easily bend. As a result, it is possible to ensure lubricity of guide wire within the blood vessel while also enabling the guide wire to follow the shape of the blood vessel in which it is inserted.

Abstract: A wire guide and methods for making the same is provided. The method includes joining a proximal core wire comprised of a stiff material to a distal core wire comprised of a highly elastic wire material. The proximal core wire may have a recess at a distal face and the distal core wire is secured within the recess. The recess may be machined into the distal face of the proximal core wire. The distal core wire may be a coaxial wire having a sleeve of material that is easily weldable to the proximal core wire. The sleeve is welded to the proximal core wire and a distal portion of the sleeve is then removed to expose the distal core wire.

Abstract: A guidewire (10) includes a flexible elongated core (20) having a proximal end (22) and a distal end (24). An anchor wire (10) has a distal end (34) connected to the distal end (24) of the core (20) and a distally located helical portion (50) that encircles the core. The guidewire (10) has an anchoring condition in which the helical portion (50) is expanded radially away from the core (20). The guidewire (10) has an advancing condition in which the helical portion (50) is stretched longitudinally and contracted radially in response to tension on the anchor wire (30).

Abstract: Embodiments of a syringe-based device for procuring bodily fluid samples can include a housing having a port that can be coupled to a lumen-defining device for receiving bodily fluids, an actuator mechanism retained at least partially within the housing, the actuator mechanism including a pre-sample reservoir, a plunger operably coupled with pre-sample reservoir, a plunger cap, a plunger tube, a valve, a plunger seal, an a selectively attachable collection vial for capturing a bodily fluid sample.