Abstract: The present disclosure provides a container containing reference solution for clinical chemistry, whereby the container includes a closure part-covered outlet at which reference solution can be removed by puncturing with a puncturing element. The disclosure further provides a wick that is soaked with the reference solution and arranged in the container to extend from the outlet and such that a majority of its length extends into an interior space of the container.

Abstract: Sensor elements are disclosed for the electrochemically analyzing a body fluid, as well as methods of producing and using the same. The sensor elements include an electrically conductive layer structure applied to a non-conductive carrier substrate, where the layer structure includes a continuous base layer of tantalum, niobium or an alloy thereof, and a metallic cover layer formed on the base layer that covers the base layer either over the entire surface or in some regions. The metallic cover layer includes a more noble metal when compared to the base layer.

Abstract: The invention concerns a control device for a medical test system which has a lancing element that can be inserted into body tissue to collect body fluid and a lancing drive for the lancing element. A sensor element for body fluid is arranged on the lancing element and a control unit is coupled to the sensor element for detecting a fault when collecting body fluid. In order to improve the success rate, the control unit actuates the lancing drive for an automatic puncture repetition in less than 1 second when a fault, e.g., inadequate wetting of a detection field, occurs.

Abstract: Protective coverings are provided for hand-held medical devices that have a measuring port for a disposable analytical test element. The coverings also include a sleeve having a reception opening and can be slipped over the devices to at least partially enclose the devices in a usable protected state. The coverings further include a test element adapter formed as an integral part of the sleeve to receive the test element in alignment with a measuring port, where the sleeve includes the test element adapter and is arranged as a sealing barrier between the test element and the device port in a protected state.

Abstract: An automatic apparatus for obtaining and analyzing a blood sample contains a supply of lancets and test strips, which are located alternately on a carrier band. A lancet or alternatively a test strip may be clamped on a holder, which is mounted so it is movable. The movement controller of the holder comprises a three-dimensional control curve and a guide element, which engages at different depths in the control curve as a function of its relative position. The control curve comprises two guide paths, which run on different parallel planes. The contour of the first guide path determines the movement path of the lancet and the contour of the second guide path determines the movement path of the test strip. The test strip executes a transverse offset perpendicular to the puncture axis of the lancet.

Abstract: A method for producing a membrane ring or test strip ring for a diagnostic test device includes an elongate strip that is divided into segments by cuts running transversely to the longitudinal direction of the strip, where the cuts are made only as far as a residual width of the strip so that a material bridge remains intact between the segments adjacent to the cuts (24). The strip is closed by bringing its ends together to form a ring where the cut edges of the cuts running towards the material bridges each enclose an acute angle (?). The ring is inserted into a support structure as a membrane ring or test strip ring for the test device.

Abstract: A sampling system for collecting a liquid sample, having at least one analytic auxiliary means is proposed. The sampling system has a coupling element for coupling onto the analytic auxiliary means and at least one drive unit for driving a movement of the coupling element from a rest position into a deflected position. The drive unit comprises an energy transducer which is designed to generate a rotational movement with different rotational directions. The drive unit furthermore has a coupling device with at least one rotational-direction sensitive element, wherein the coupling device is designed to couple the energy transducer to a first system function in a first rotational direction, and to couple said transducer to a second system function which differs from the first system function in a second rotational direction which differs from the first rotational direction.

Abstract: A method for sterilizing an implantable sensor for sensing an analyte in a body tissue. The implantable sensor has a sensor part which can be introduced into the body tissue, at least one sensor electrode for sensing the analyte, and at least one electronics part. The electronics part has at least one electronic component and is connected to the sensor part. The method includes (a) introducing the implantable sensor into a package, the package sealing the implantable sensor from bacteria and accommodating a radiation shield, (b) irradiating the implantable sensor in the package with sterilizing radiation from at least one irradiating direction, in particular with electron radiation, the radiation shield shielding the electronic component of the electronics part from the sterilizing radiation, the radiation shield being arranged in such a way that the sensor part is sterilized by the sterilizing radiation.

Abstract: A method for making a dry sensor element for an enzymatic determination of an analyte in a body fluid includes providing a substrate, producing a working electrode on the substrate, comprising depositing an active enzymatic electrode layer on a working electrode base structure provided on the substrate, the active enzymatic electrode layer containing an enzyme, producing a counter electrode on the substrate, and producing electric connectors on the substrate connected to the working electrode and the counter electrode, wherein the step of depositing the active enzymatic electrode layer on the working electrode base structure comprises depositing PEDOT:PSS by electropolymerization. A dry sensor element for an enzymatic determination of an analyte in a body fluid is also disclosed.

Abstract: A puncturing system for obtaining a sample of body fluid comprises a magazine that comprises a lancet carrier that carries several lancets, a puncturing device comprising a compartment for the magazine, an incremental advancing mechanism for moving the lancets successively to a puncturing position, and a puncturing drive for accelerating one of the lancets that is positioned in the puncturing position in a puncturing motion. The magazine comprises a coupling facility with a receptacle for the lancet carrier. The receptacle is mobile with respect to a magazine housing The lancets that are carried by the lancet carrier can be moved relative to the receptacle by actuating the incremental advancing mechanism The receptacle is adapted to couple the puncturing drive to one of the lancets positioned in the puncturing position for transmitting a driving force generated by the puncturing drive during a puncture to the lancet positioned in the puncturing position.

Abstract: A test strip for analyzing a biological fluid using a test meter includes a biosensor to sense the biological fluid. The test strip includes contacts to communicate with the test meter and conductors connected to the contacts. The test strip further includes a combination of diodes, resistors, and short circuits arranged in various ways between the conductors. The test strip stores data based on a number of connections severed between the diodes, the resistors, the short circuits, and the conductors. The test meter reads the data and communicates with the biosensor via the contacts.

Abstract: A tape cassette for a medical handheld device is disclosed as comprising a carrier tape, which carries test fields for assaying a sample of a human or animal bodily fluid and/or lancets as functional elements, a supply chamber, in which a supply section of the carrier tape comprising unused functional elements is positioned, a winding unit, in order to wind up the carrier tape and draw it through a tape exit opening of the chamber, so that the functional elements may be brought sequentially into a usage position. The carrier tape in the tape exit opening is oriented transversely to the supply section positioned in the supply chamber.

Abstract: A puncturing system includes a carrier tape carrying multiple lancets and having position marks, a housing comprising a conveying facility for positioning the lancets and a housing opening, a puncturing drive for accelerating a lancet positioned in a usage position, a storage medium for storing distance values that depend on distances between the lancets of the carrier tape and position marks allocated to the respective lancets, a sensor for detecting position marks in a detection position through which the position marks proceed upon motion of the carrier tape, and a control unit that controls the conveying facility. To position a lancet in the usage position, the control unit stops the conveying facility upon the carrier tape moving a positioning distance. The length of the positioning distance depends on the distance between the lancet to be positioned and the detected position mark and is determined by the control unit.

Abstract: Certain exemplary embodiments include a test element operable to receive a sample and to provide an indication of an analyte of the sample to a meter. In one form test element comprises a substrate and an optically readable pattern provided on the substrate which encodes information relating to the test element.

Abstract: A pricking system includes lancets for producing a prick wound, sampling devices for collecting a sample of a body fluid from the prick wound, a housing having an opening for application of a body part in which the prick wound is to be produced, a drive arranged in the housing for moving one of the lancets to produce the prick wound and to then move one of the sampling devices to the prick wound so produced, a coupling part for coupling to the drive one of the lancets for a pricking movement and then coupling to the drive one of the sampling devices for a sampling movement, the coupling part being moved, during the pricking movement and the sampling movement, respectively, from a starting position into an end position by an advancing movement, and from the end position back into the starting position by a reversing movement, respectively, and a motion control which, during the sampling movement, causes the coupling part to reach an end position that differs from the end position reached by the coupling part d

Abstract: Sensor elements are disclosed for the electrochemically analyzing a body fluid, as well as methods of producing and using the same. The sensor elements include an electrically conductive layer structure applied to a non-conductive carrier substrate, where the layer structure includes a continuous base layer of tantalum, niobium or an alloy thereof, and a metallic cover layer formed on the base layer that covers the base layer either over the entire surface or in some regions. The metallic cover layer includes a more noble metal when compared to the base layer.

Abstract: An automatic apparatus for obtaining and analyzing a blood sample contains a supply of lancets and test strips, which are located alternately on a carrier band. A lancet or alternatively a test strip may be clamped on a holder, which is mounted so it is movable. The movement controller of the holder comprises a three-dimensional control curve and a guide element, which engages at different depths in the control curve as a function of its relative position. The control curve comprises two guide paths, which run on different parallel planes. The contour of the first guide path determines the movement path of the lancet and the contour of the second guide path determines the movement path of the test strip. The test strip executes a transverse offset perpendicular to the puncture axis of the lancet.

Abstract: A method for manufacturing a device for monitoring at least one body function of a user comprising providing an evaluation unit, providing a sensor unit, aligning a connector portion of the sensor unit next to an electric contact pad of the evaluation unit such that the connector portion faces the electric contact pad, providing at least one anisotropic conductive adhesive between the electric contact pad and the connector portion, and bonding the evaluation unit substrate and the connector substrate together, wherein the electric contact pad and the connector portion are pressed together, and wherein an electric connection of the electric contact pad and the connector portion is created via the anisotropic conductive adhesive.

Abstract: A test strip for analyzing a biological fluid using a test meter includes a biosensor to sense the biological fluid. The test strip includes contacts to communicate with the test meter and conductors connected to the contacts. The test strip further includes a combination of diodes, resistors, and short circuits arranged in various ways between the conductors. The test strip stores data based on a number of connections severed between the diodes, the resistors, the short circuits, and the conductors. The test meter reads the data and communicates with the biosensor via the contacts.

Abstract: Lancets comprising a piercing element for puncturing the skin of a patient, a test region containing detection reagents for determining an analyte concentration of a body fluid sample, a capillary structure arranged in the piercing element for transporting a body fluid sample to the test region, and a sterile protection element, which encloses the tip of the piercing element. The capillary structure is blocked in a section surrounded by the sterile protection element. Also provided are methods for producing a lancet, comprising: producing a piercing element, which on the upper side has an upwardly open capillary structure; covering a section of the upper side of the piercing element and blocking the capillary channel in this section using a first material; covering a section of the underside using a second material; sterilizing the piercing element; and attaching a test region containing detection reagents to the piercing element.