Abstract: An electronic device includes a seal compressed between a moveable structure and a support. A retainer maintains seal compression in a first direction absent force exerted on the moveable structure. However, the retainer allows increased seal compression by moving in a second, opposing direction when force is exerted on the moveable structure. A force sensor (positioned internal to the seal) is influenced by movement of the moveable structure in response to the force and a signal received from the force sensor indicates an amount of the force. By maintaining the seal in compression but allowing further compression, the seal can hermetically seal the electronic device against contaminant entry without adversely impacting detection of the amount of force.

Abstract: An electronic device includes a seal compressed between a moveable structure and a support. A retainer maintains seal compression in a first direction absent force exerted on the moveable structure. However, the retainer allows increased seal compression by moving in a second, opposing direction when force is exerted on the moveable structure. A force sensor (positioned internal to the seal) is influenced by movement of the moveable structure in response to the force and a signal received from the force sensor indicates an amount of the force. By maintaining the seal in compression but allowing further compression, the seal can hermetically seal the electronic device against contaminant entry without adversely impacting detection of the amount of force.

Abstract: A diagnostic test strip vial has a container, a lid, and a plurality of diagnostic test strips. The container has a generally annular wall that terminates at a base and at an open mouth at an end that is opposite the base. The annular wall is cut at an oblique angle creating a wall that has a high side and a low side at the open mouth. The low side of the annular wall of the container is shorter in length than a diagnostic test strip that enclosed in the vial when the lid is closed with the container.

Abstract: A lancing device is used with a lancet for lancing body tissue to result in a wound for bleeding. The lancing device has a cantilevered priming arm having a first arm portion that is generally parallel to an internal channel of the device and a second arm portion that is generally perpendicular to the internal channel. The second arm portion is connected to a lancet carrier and movement of the first arm portion toward the internal channel draws the lancet carrier to a primed position and stores energy in a lancet driver.

Abstract: A lancet cartridge has a U-shaped support with a pair of anchor portions, a base portion, and a pair of deformable leg portions connecting the anchor portions to the base portion. The pair of deformable leg portions change shape from an initial shape to an extended shape in response to an external applied force and recover to a retracted shape upon removal of the force. The lancet cartridge also has a lancet having a tip end, an opposing base end, and an axis extending between the tip end and the base end. A portion of the lancet is disposed between the pair of deformable leg portions of the U-shaped support. The lancet is movable between a starting position, an extended puncturing position, and an ending position along the axis of the lancet in a path defined by the U-shaped support. When the lancet is in the starting position, the tip end of the lancet is disposed at least partially through the base portion of the U-shaped support, and the U-shaped support is in the initial shape.

Abstract: A lancing device is used with a lancet for lancing body tissue to result in a wound for bleeding. An improved lancing device has a priming knob having a slanted priming notch rotatably connected to the lancing device about an axis of rotation generally parallel to a central axis of the lancing device and a strike path of a lancet carrier. Rotation, translation, or both rotation and translation of the priming knob allows a user to prime the lancing device.

Abstract: A lancet cartridge has a U-shaped support with a pair of anchor portions, a base portion, and a pair of deformable leg portions connecting the anchor portions to the base portion. The pair of deformable leg portions change shape from an initial shape to an extended shape in response to an external applied force and recover to a retracted shape upon removal of the force. The lancet cartridge also has a lancet having a tip end, an opposing base end, and an axis extending between the tip end and the base end. A portion of the lancet is disposed between the pair of deformable leg portions of the U-shaped support. The lancet is movable between a starting position, an extended puncturing position, and an ending position along the axis of the lancet in a path defined by the U-shaped support. When the lancet is in the starting position, the tip end of the lancet is disposed at least partially through the base portion of the U-shaped support, and the U-shaped support is in the initial shape.

Abstract: A lancing device is used with a lancet for lancing body tissue to result in a wound for bleeding. The lancing device has a cantilevered priming arm having a first arm portion that is generally parallel to an internal channel of the device and a second arm portion that is generally perpendicular to the internal channel. The second arm portion is connected to a lancet carrier and movement of the first arm portion toward the internal channel draws the lancet carrier to a primed position and stores energy in a lancet driver.

Abstract: A lancing device is used with a lancet for lancing body tissue to result in a wound for bleeding. An improved lancing device has a priming knob having a slanted priming notch rotatably connected to the lancing device about an axis of rotation generally parallel to a central axis of the lancing device and a strike path of a lancet carrier. Rotation, translation, or both rotation and translation of the priming knob allows a user to prime the lancing device.

Abstract: A test strip vial has a container, a test strip magazine disposed within the container, and a lid. The magazine has a plurality of test strip slots radially disposed about an axis of the magazine and extending through the first end of the magazine. The lid is rotatably attached about the open end of the container and has a test strip aperture defined therein that is sequentially aligned with each of the test strip slots as the lid is rotated. The vial also has an incremental rotation mechanism associated therewith that permits incremental rotation of the lid relative to the magazine to sequentially align the aperture with each of the slots. Test strips are individually disposed within the slots.

Abstract: A storage container for storing used diagnostic test strips has a base wall, a top wall, and a side wall that define an enclosed container space. The container has formed therein a test strip opening that connects the outside environment with the enclosed container space. The test strip opening is sized to receive a test strip and allow its passage from the outside environment to the enclosed container space. The test strip opening is disposed on the container in a position to restrain a test strip disposed in the container space from falling out of the container through the test strip opening, or the test strip opening is shaped to restrain a test strip disposed in the container space from falling out of the container through the test strip opening, or both.

Abstract: A diagnostic test strip vial has a container, a lid, and a plurality of diagnostic test strips. The container has a generally annular wall that terminates at a base and at an open mouth at an end that is opposite the base. The annular wall is cut at an oblique angle creating a wall that has a high side and a low side at the open mouth. The low side of the annular wall of the container is shorter in length than a diagnostic test strip that enclosed in the vial when the lid is closed with the container.