Abstract: An electrical connecting cable with a flexible electrical cable and with at least one electrical plug connector at one end of the cable, with the electrical cable including a bundle of conductors consisting of insulated stranded wires, a foil shield enclosing the bundle of conductors, and a protective sheath encasing the foil shield and serving as the outer surface of the cable. The plug connector includes a metallic plug connector housing, preferably a round housing, holding insulated contacts and a molded-on shield sleeve with which the stranded wires and the foil shield are connected in an electrically conductive manner. The foil shield includes at least one electrically conductive shield tape and the protective sheath includes at least one electrically non-conductive sheath tape that are both wrapped at an angle spiral-like with a lateral overlap along the stranded wires around the bundle of conductors and the shield sleeve.

Abstract: A device for performing at least one medical function on a user is proposed. The device has at least one medical functional element that is designed to perform the medical function. The medical function is selected from a diagnostic, a therapeutic and a surgical function. The device has at least one evaluation and control part that comprises at least one actuation component for controlling the medical function. The evaluation and control part has at least one casing and at least one battery receptacle. The battery receptacle comprises at least one electrical energy reservoir, more particularly at least one battery. The battery receptacle is designed to be opened irreversibly by the user for removing the energy reservoir.

Abstract: A medical device for carrying out at least one medical function. The medical device comprises at least one control part, which can be applied to a body surface of a user, and at least one functional element, which can be inserted into a body tissue of the user at at least one insertion site. The functional element can be connected to the control part. The functional element is designed to carry out at least one medical function. The control part has at least one base part with at least one supporting surface, which faces the body surface. The base part has at least one collection channel for collecting bodily fluid emerging from the insertion site.

Abstract: Method for the injection-molding production of a magazine having a plurality of chambers, separated by partition walls, including an outer wall formed by an outer wall of the magazine. The method uses a casting mold having an outer wall channel corresponding to the outer wall of the magazine, and partition wall channels corresponding to the partition walls, and a gate opening. A plurality of partition wall channels extend from the gate opening to the outer wall channel. The method comprises injecting a plastic compound into the gate opening. The plastic compound flows from the gate point to the partition wall channels into the outer wall channel. The plastic compound streams have a differing flow speed in alternating partition wall channels so a joint line, which is aligned with a partition wall channel, forms on the outer side of the outer wall channel.

Abstract: A system for determining an analyte in a body fluid includes a magazine comprising two partial magazines, one including chambers containing analysis elements having a sample contact zone and a reagent system containing a reagent, whose reaction with the body fluid results in a change of a variable, and another including chambers containing puncturing elements having a tip having a capillary channel, which forms a fluid connection between the tip and a sample transfer zone of the puncturing element. The system may also include an analysis instrument having a puncturing drive for driving a puncturing element on a movement path, a mounting for receiving the magazine such that one chamber of the magazine at a time is located in a functional position, in which a puncturing element in the chamber can be moved by the puncturing drive, and a measuring and evaluation apparatus for measuring the change of the variable.

Abstract: An instrument for producing a sample of body fluid for analysis by piercing the skin with a lancing element having a piercing tip is disclosed. The instrument can comprise a housing and a lancing drive for driving a lancing element connected thereto in a puncturing movement. A pressure ring can surround a skin contact opening and can be adapted for pressing against the skin such that the skin can bulge into the skin contact opening for promoting expression of body fluid. The skin contact opening can have a circular opening with a diameter of at least about 3 mm and at most about 8 mm. The instrument can comprise a pressing force control device for controlling the pressing force between the pressure ring and the skin at the time of triggering the puncturing movement, to be at least about 3 N and at most about 8 N.

Abstract: A lancet wheel having a rim with a plurality of lancets extending radially inward from the rim is dropped in a circular frame having a plurality of spokes forming a plurality of chambers for facilitating drop-in assembly of the modular lancet wheel with the frame. A test ring having a plurality of test sections is assembled on the frame such that one test section is located adjacent each lancet to form an integrated cartridge. Each lancet includes a lancet tip defining a capillary groove sized to collect a body fluid sample from the incision via capillary action. The lancet tip exits the chamber to form the incision in skin, the capillary groove collects the body fluid sample, the lancet tip retracts into the chamber, and a portion of the lancet contacts the test section to transfer the sample from the capillary groove to the test section to analyze the sample.

Abstract: Analysis system for determining an analyte in a body fluid is presented. The system comprises a reusable analysis instrument and a magazine having a plurality of integrated sample acquisition and analyzing elements. Each element comprises a puncturing element and an analyzing element. A coupling unit couples the integrated sample acquisition and analyzing element to a drive. The magazine comprises a housing having a plurality of elongate neighboring chambers separated by two side walls running in a longitudinal. The chambers contain the integrated sample acquisition and analyzing element. The chambers have an exit opening allowing for the at least partial exiting of the puncturing element. The chambers of the magazine are accessible to a coupling element that can be formfitting coupled to the coupling structure of the puncturing element, when the puncturing element is in the chamber of the magazine and the magazine is located in a holder.

Abstract: The invention relates to a portable hand-held analytical device for analysis of a medically significant component of a sample, the device including a housing having a loading opening for receiving a replaceable drum cartridge containing analytical consumables, whereby the housing comprises on an outer side a dispensing opening through which the consumables can be pushed by means of a removal facility. The device includes a loading opening which is closeable by means of a lid, which upon closing effects a linear motion of a pushing part which moves the drum cartridge to a working position, in which it can be rotated about its geometric longitudinal axis.

Abstract: A disposable device for analyzing body fluid especially for blood sugar tests includes a container which can be inserted into a measuring apparatus, a sampling member provided in the container to pierce skin of a body part and sample body fluid, and a test member for receiving body fluid obtained by the skin-piercing. In one form, the test member is fixed in a retaining chamber of the container, and the sampling member is configured in the same retaining chamber such that it is separated at a distance from the test member in an initial state and is in contact with the test member to transfer body fluid in a transfer state after the skin-piercing.

Abstract: The invention relates to a method of design of ruled surfaces. The method comprises the step of accessing data defining guiding curves P(u) and Q(v) and a cost function f(t, w). Given P(u) and Q(v), the unknown coupling is a parameterized curve s(t(s), w(s)). The method further comprises defining an objective function of the type J=J(f, t, w), involving both f(t, w) and coordinates t, w of the coupling curve. Then, optimizing the objective function J makes it possible to obtain the target coupling curve. Finally, a ruled surface S(s, ?)=Q(w(s))+(1??)P(t(s)) is provided, according to the guiding curves P(t(s)) and Q(w(s)), composed with the coordinates t, w of the coupling curve previously obtained. The objective function is further constrained at the optimization step such that arguments t, w of the cost function f(t, w) are regulated by a regulation function ?.

Abstract: At least one server is queried from a wireless device to obtain program data, and to obtain DVR data from a digital video recorder. The program data is received from the server and the DVR data is received from the digital video recorder The program data and/or the DVR data are displayed on the wireless device. The at least one digital video recorder is controlled by selecting a user-operable function from the program data and/or the DVR data on the wireless device.

Abstract: A measurement system is provided which comprises an analysis device with at least one of a measurement function and a sample collection function, and also at least one magazine configured to receive at least one consumer element therein. The magazine comprises a magazine housing having a pair of openings. The magazine is designed as an exchangeable magazine that can be selectively operatively connected to the analysis device. The analysis device further comprises a closure mechanism having at least one sealing element which is designed to convey at least one consumer element from one of the openings. The sealing element is further configured to sealingly close the openings of the magazine when the sealing element is disposed therein.

Abstract: A method and a device for an open-load diagnosis of a switching stage includes the steps of turning off the switching transistor if, after a first delay time has elapsed since an appearance of a control signal, the output voltage is less than a first reference voltage, and if, after a second delay time has elapsed, the output voltage is less than a second reference voltage, then, with the switching transistor in the on state again, comparing the output current flowing through the switching transistor with a reference current, and if the output current is less than the reference current, effecting an open-load indication. The device includes a switchable buffer amplifier; a switching transistor, second and third transistors, a reference current source, first and second comparators, and a control circuit connected to the buffer amplifier, to the second and third transistors, and to the first and second comparators.

Abstract: A method and a device for an open-load diagnosis of a switching stage includes the steps of turning off the switching transistor if, after a first delay time has elapsed since an appearance of a control signal, the output voltage is less than a first reference voltage, and if, after a second delay time has elapsed, the output voltage is less than a second reference voltage, then, with the switching transistor in the on state again, comparing the output current flowing through the switching transistor with a reference current, and if the output current is less than the reference current, effecting an open-load indication. The device includes a switchable buffer amplifier; a switching transistor, second and third transistors, a reference current source, first and second comparators, and a control circuit connected to the buffer amplifier, to the second and third transistors, and to the first and second comparators.

Abstract: This invention relates generally to in vitro methods for inducing or enhancing expression of enteric bacterial antigens and/or virulence factors thereby producing antigenically enhanced enteric bacteria, to methods for using antigenically enhanced enteric bacteria and to vaccines comprising antigenically enhanced enteric bacteria. A Shigella bacterium having enhanced antigenic property is disclosed. A culture medium useful for culturing the Shigella comprises 0.05% to 3% bile or 0.025% to 0.6% of one or more bile acids or salts. In addition a divalent cation chelator can also be included in the culture medium. The bacteria culture is in a growth phase at early log phase and between early log phase and stationary phase. The enhanced antigenic property is a higher level of an immunogenic antigen when compared to the antigenic property of the same bacteria grown on brain heart infusion broth. Also, antibodies to Shigella bacteria or Shigella bacteria in samples are detected by immunoassays.

Abstract: This invention relates generally to in vitro methods for inducing or enhancing expression of enteric bacterial antigens and/or virulence factors thereby producing antigenically enhanced enteric bacteria, to methods for using antigenically enhanced enteric bacteria and to vaccines comprising antigenically enhanced enteric bacteria. A Campylobacter bacterium having enhanced antigenic property is disclosed. A culture medium useful for culturing the Campylobacteria comprises 0.05% to 3% bile or 0.025% to 0.6% of one or more bile acids or salts. In addition a divalent cation chelator can also be included in the culture medium. The bacteria culture is in a growth phase at early log phase and between early log phase and stationary phase. The enhanced antigenic property is a higher level of an immunogenic antigen when compared to the antigenic property of the same bacteria grown on brain heart infusion broth. Also, antibodies to Campylobacter bacteria or Campylobacteria in samples are detected by immunoassays.

Abstract: Methods using in vitro processes are disclosed for inducing or enhancing expression of enteric bacterial antigens or virulence factors. The methods, therefore, produce antigenically enhanced enteric bacteria. Also methods for using the antigenically enhanced bacteria are also disclosed, as well as vaccines containing the enteric bacteria. Specifically a whole enteric bacterium or components thereof are provided by Helicobacter species. Also there are other enteric bacteria which are useful for the disclosed invention; such as Campylobacter jejuni.

Abstract: Methods using in vitro processes are disclosed for inducing or enhancing expression of enteric bacterial antigens or virulence factors. The methods, therefore, produce antigenically enhanced enteric bacteria. Also disclosed are methods for using the antigenically enhanced bacteria, as well as vaccines containing the enteric bacteria. Specifically, a whole enteric bacteria or components thereof are provided by Campylobacter species. In addition to this species there are other enteric bacteria, such as Yersinia spp., Bacteroides spp., Klebsiella spp., Gastrospirillum spp., Enterobacter spp., Salmonella spp., Aeromonas spp., Vibrio spp., Clostridium spp., Enterococcus spp., and Escherichia coli, which are useful for inducing or enhancing expression of enteric bacterial antigens and/or virulence factors.

Abstract: Methods using in vitro processes are disclosed for inducing or enhancing expression of enteric bacterial antigens or virulence factors. The methods, therefore, produce antigenically enhanced enteric bacteria. Also methods for using the antigenically enhanced bacteria are also disclosed, as well as vaccines containing the enteric bacteria. Specifically, a whole enteric bacteria or components thereof are provided by Helicobacter species. Also there are other enteric bacteria which are useful for the disclosed invention; such as Campylobacter jejuni.