Abstract: A vascular access wire is disclosed. The vascular access wire includes an elongated core member and a distal tip. The Distal tip comprising a crank configured with a crank distal surface and a crank center of rotation. The crank is configured to rotate about the crank center of rotation when the core member is sufficiently loaded axially and when the crank distal surface is pressed against a wall of a target blood vessel, for triggering or affecting a deflecting and/or a deforming of the core member proximally to the crank.

Abstract: The present invention relates generally to safety face shield devices and more particularly to face shield devices comprising a single lens piece that conforms to the curvature at approximately the midpoint of wearer's frontal bone extending bilaterally around the wearer's face towards the temporal bones. In preferred embodiments, the safety face shield devices comprise a single lens piece (i.e., one piece) that is removably, or permanently, attached to a one piece substantially u-shaped supporting frame member through a plurality of attachment points (e.g., press fit tapered knobs). The present face shield protects the wearer's eyes, nose, mouth, and ears from direct as well as arching splashes, sprays, spatters and droplets of various liquid and semiliquid materials, and more particularly, from biological derived materials, liquids, and semiliquid materials, such as saliva, blood, mucus (e.g., nasal discharge and rhinorrhea), urine, and the like.

Abstract: A respiratory protection mask is disclosed. In one example, the respiratory protection mask comprises an upper portion, a lower portion, and a respiratory filter. The respiratory filter comprises an air outlet, and is arranged in, on and/or at the upper portion such that an inhaled airflow can run substantially straight from the air outlet of the respiratory filter through the upper portion, towards the lower portion and/or to a nose of a mask wearer when the respiratory protection mask is worn by the mask wearer.

Abstract: An eye shield dispenser having an outer box and a holder within the outer box for holding eye shields. The holder is configured to hold the eye shields horizontally along an upper surface of the holder and to position the eye shields proximate an opening in the outer box through which the eye shields may be retrieved.

Abstract: A guidewire for vascular access has an elastically articulatable tip configured to minimize risk of vessel wall damage during initial insertion of the guidewire into the vasculature of a patient. The guidewire may have a local flexible portion in a tip segment of the guidewire and/or a core thereof.

Abstract: An eye shield dispenser having an outer box and a holder within the outer box for holding eye shields. The holder is configured to hold the eye shields horizontally along an upper surface of the holder and to position the eye shields proximate an opening in the outer box through which the eye shields may be retrieved.

Abstract: Provided is a service architecture support method with which the content of a new service provided by an application incorporated into a medical/nursing support system can be finely adjusted according to the needs of a patient or a person requiring care, or a medical professional or a nurse. To that end, when an application (220) developed using an application framework (200) is incorporated into a medical/nursing support system (30), an application ID is allocated to the application (220) and the application ID is associated with a group ID and stored, thereby enabling selective use of a new service provided by the application (220) by only a group member of a group with which the application ID has been associated. Furthermore, the specific function installed in the application (220) can be set in administrator settings according to the needs of a patient or a medical professional from said group.

Abstract: A medical/care support method is provided, which enables medical or care workers having different special fields such as physicians and nurses to share the medical or care information of each patient or care-needing person while protecting the privacy of the patient or care-needing person, and to support the provision of better-quality medical or care service to the patient or care-needing person based on the medical or care information shared. A patient ID, a disease ID, and a medical facility ID are associated and stored, thereby generating a group G11. A patient P1 designated by patient group registration participates in the group G11 after the patient's approval of an invitation request. Medical workers M1 and M2 and patient-related persons R1, R2, and R4 participate in the group G11 as supporters in response to respective invitation requests.

Abstract: A system and method for thermal regulation, the system comprising a bedding element that is configured to enclose at least a part of a living being or other object. The system further comprising a temperature regulation element that is included in the bedding element and that includes a phase change material which changes between a liquid phase and a solid phase within the desired temperature range.

Abstract: A medical/care support method is provided, which enables medical or care workers having different special fields such as physicians and nurses to share the medical or care information of each patient or care-needing person while protecting the privacy of the patient or care-needing person, and to support the provision of better-quality medical or care service to the patient or care-needing person based on the medical or care information shared. A patient ID, a disease ID, and a medical facility ID are associated and stored, thereby generating a group G11. A patient P1 designated by patient group registration participates in the group G11 after the patient's approval of an invitation request. Medical workers M1 and M2 and patient-related persons R1, R2, and R4 participate in the group G11 as supporters in response to respective invitation requests.

Abstract: Infant warming systems are described herein generally comprising a temperature regulation assembly which encloses a phase change material (PCM). The temperature regulation assembly may be initially heated (or re-heated) by water contained within a heating assembly and then placed within a retaining pouch of an infant bedding. The PCM may then provide constant heat over a period of time to the infant. A control/indicator interface coupled to the regulation assembly may constantly monitor the temperature of the PCM as well as the ambient temperature to provide one or more indications or alerts to the user with respect to one of several states of the warming assembly.

Abstract: Systems and methods are disclosed for regulating body temperature. The system includes a housing that comprises compartments for a phase change material and a heat transfer material. The compartments are configured to transfer heat from the heat transfer material to the phase change material. A temperature sensor is used to determine when the phase change material has reached a pre-determined temperature. When the pre-determined temperature is reached, a release mechanism or lever is coupled to the temperature sensor to separate the phase change material compartment from the heat transfer material compartment or to remove the heat transfer material away from the phase change material compartment. The heated phase change material compartment can be used to regulate body temperature.

Abstract: Systems and methods are disclosed for regulating body temperature. The system includes a housing that comprises compartments for a phase change material and a heat transfer material. The compartments are configured to transfer heat from the heat transfer material to the phase change material. A temperature sensor is used to determine when the phase change material has reached a pre-determined temperature. When the pre-determined temperature is reached, a release mechanism or lever is coupled to the temperature sensor to separate the phase change material compartment from the heat transfer material compartment or to remove the heat transfer material away from the phase change material compartment. The heated phase change material compartment can be used to regulate body temperature.

Abstract: A system and method for thermal regulation, the system comprising a bedding element that is configured to enclose at least a part of a living being or other object. The system further comprising a temperature regulation element that is included in the bedding element and that includes a phase change material which changes between a liquid phase and a solid phase within the desired temperature range.

Abstract: An apparatus to relieve menstrual cramping includes one or more tapered pads having an inner and outer side, each outer side being semi-rigid and each inner side being flexible. The outer side of each pad is connected to one or more straps having first and second ends. A fastener is attached to the first end of each strap and a corresponding second fastener attaches to the second end of each strap. The apparatus includes a variable compression drive located proximate to one pad to create a compression force through each strap when the first and corresponding second fasteners connect. The drive includes an outer drum shell, an inner rotator having an inner diameter that is treaded, a motor which communications with the inner rotator, and a threaded shaft which engages the inner diameter of the inner rotator. A tab attaches the threaded shaft to the strap.

Abstract: An apparatus to relieve menstrual cramping which includes one or more symmetrical tapered pads having an inner and outer side, each outer side being semi-rigid and each inner side being flexible and compressible. The outer side of each pad is connected to one or more straps having a first and corresponding second end. A fastener is attached to the first end of each strap and a corresponding second fastener attaches to the second end of each strap. The apparatus also includes a constricting device (such as a ratchet) located on or proximate to one pad sufficient to create a compression force through each strap when the first and corresponding second fasteners connect to one another. The corresponding method includes the steps of placing one or more pads proximate to the hips, affixing each pad to each strap, connecting both ends of the straps to each other and creating necessary compression.

Abstract: A compression undergarment to relief the symptoms of menstrual cramping may comprise a first and second pad both capable of conforming to a female user's hips. Each pad is tapered having two part construction. Such construction may include a pliable exterior panel of resilient material and an interior panel made of compressible material. The second component of the apparatus is a compression undergarment having a first and corresponding second annular sleeve. Such compression undergarment includes a front side, back side, first leg portion and second leg portion, such that positioned above the first leg portion and second leg portion is a top portion which connects both leg portions. The compression undergarment also includes a first annular sleeve capable of receiving the first pad and the second annual sleeve capable of receiving the second pad. The third component is a compression band that fits around both pads and the compression undergarment.