Abstract: The present invention provides an integrated measuring device that includes a blood collection system for collecting blood for diagnostic purposes. The blood collection system comprises an electric motor which provides energy for propelling a lancet. The blood collection system comprises a mechanical energy store in which the electric energy that is converted by the motor is stored in the form of mechanical energy. The use of a mechanical energy store allows the use of known mechanical drive elements. The blood collection system can also be electrically activated and is thus easy to use for the operator. The motor can also be coupled to another system component, such as a test strip or lancet drum, to operate it.

Abstract: A control solution packet for calibrating a bodily fluid sampling device includes a container, a control solution pressurized within the container, and a membrane for covering and sealing the container. The control solution can be pressurized before or during calibration so as to ensure the appropriate amount of control solution is delivered to the bodily fluid sampling device. The control solution is manufactured to have a viscosity that controls delivery of the control solution to the device. The membrane is permeable by a piercing device of the bodily fluid sampling device and seals around the piercing device during calibration. In another aspect, the container is in the form of a capsule or dosing attachment that contains the control solution along with a sponge-like material.

Abstract: The invention relates to a system for withdrawing body fluid from a body part via a withdrawal site located on the surface of the body part, with at least one sensor for detecting at least one variable dependent on the location or state of the withdrawal site, and with an evaluation unit for evaluating the at least one variable detected by the at least one sensor and for triggering a reaction, dependent on the value of the detected variable, in the system for withdrawing body fluid, said reaction serving to prepare the system for puncturing the surface of the body part, and with at least one puncturing device for creating an opening in the body at the withdrawal site. The invention further relates to an integrated analysis system, to a method for configuring a system for withdrawal of body fluid, and to a method for selecting a menu item from a menu for controlling a system for withdrawing body fluid from a body part.

Abstract: A measurement system and method for operating a measurement system is disclosed for an analyte determination. The system includes an analysis unit, which is configured to determine a measured analyte value for a body fluid specimen that is applied, a fingerprint sensor, which is configured to detect fingerprint sensor signals for one or various users, and a control unit, which is connected to the analysis unit and the fingerprint sensor unit for data transmission. The control unit is configured to perform a user identification using the detected fingerprint sensor signals and after successful user identification to enable a determination of a measured analyte value with the analysis unit for an identified user. The control unit is additionally configured to analyze the detected fingerprint sensor signals and optionally additional detected fingerprint sensor signals in addition to the user identification in order to provide control signals for performing additional measurement system functions.

Abstract: Methods for providing an estimated or predicted biological values in a sectioned display to assess the relative impact of a set of variables include collecting biological measurements, grouping the biological measurements based on the set of variables, evaluating the biological measurements to determine grouped estimated biological values or grouped predicted biological values, and providing the grouped estimated biological values or grouped predicted biological values within a plurality of sections in the sectioned display, wherein the plurality of sections correspond to the set of variables.

Abstract: The invention relates to a hand-held analytical device for analyzing a sample, in particular a biological fluid, for a medically significant component, comprising a housing comprising a loading opening for receiving a replaceable cartridge having multiple chambers that may contain analytical consumables, in particular test strips, and each chamber comprising an opening on at least one face of the cartridge and each opening may be sealed by a sealing foil, a removal facility for removing one of the analytical consumables from the cartridge. The removal facility can be used to remove one of the consumables from one of the chambers of the cartridge, in the process of which the opening sealed by the sealing foil is opened. A drive allows the cartridge to be moved in order to position one chamber in a removal position in which a consumable can be removed from the chamber by the removal facility.

Abstract: Embodiments of a testing method suitable for diabetic persons to optimize their administered insulin dosage comprise collecting one or more sampling sets of biomarker data, wherein each sampling set comprises a sufficient plurality of non-adverse sampling instances and wherein each sampling instance comprises an acceptable biomarker reading at a single point in time recorded upon compliance with adherence criteria, determining a biomarker sampling parameter from each sampling set, comparing the biomarker sampling parameter to a target biomarker range, calculating an insulin adjustment parameter associated with the biomarker sampling parameter if the biomarker sampling parameter falls outside the target biomarker range, adjusting the insulin dosage by the insulin adjustment parameter if the biomarker sampling parameter falls outside the target biomarker range and if the insulin dosage does not exceed maximum dosage, and exiting the testing method if the adjusted insulin dosage is optimized.

Abstract: A structured testing method for diagnostic or therapy support of a patient with a chronic disease and devices thereof are disclosed which implement a structured collection procedure based on a medical use case and/or question which provides at least one or more parameters defining entry criterion, a schedule of events, adherence criterion, and exit criterion. The entry criterion establish conditions needed to be met prior to obtaining biomarker data from the patient. Each event can include one or more of a performance time, patient guidance to perform the event, a request for information from the patient a request for patient action, and a request for collection of biomarker data from the patient. The adherence criterion can be used to assess whether an event performed is acceptable to addressing the medical use case and/or question, and the exit criterion establishes conditions needed to be met prior to exiting the collection procedure.

Abstract: Embodiments related to a system and method managing the implementation, execution, data collection, and data analysis of a structured collection procedure running on a portable, hand-held collection device are disclosed. The collection device performing the structured collection procedure has program instructions that when executed by a processor causes the processor to initiate automatically a schedule of events of the structured collection procedure upon one or more entry criterions being met at some unknown time, store in memory patient data collected in accordance to the schedule of events, end automatically the structured collection procedure upon one or more exit criterions being met at some unknown time, and mark/indicate the structured collection procedure as completed if no exception occurred during performance of an event in the schedule of events.

Abstract: The invention refers to an injection device for the injection of a medical agent, in particular insulin, comprising: a housing, a reception compartment for a vial containing the agent to be injected, advancement mechanics for moving an injection needle that is inserted in the device in a direction of puncturing, and a pressing facility for pressing agent from a vial that is inserted in the reception compartment for the purpose of an injection process. The advancement mechanics, effects, in a first device function for an injection process, a first motion profile of an inserted injection needle, in which a resting phase follows after an advancement motion, during which resting phase the inserted injection needle for an injection process is at rest with respect to the device housing, and effects, in a second device function for obtaining a body fluid sample for diagnostic purposes, a second motion profile of an inserted injection needle, in which a returning motion follows immediately after a puncturing motion.

Abstract: A medical device is provided, comprising a data management unit for providing patient data regarding a patient's health and/or treatment status, a display for displaying the patient data provided by the data management unit, and an actuator configured to cause one or both of activation and deactivation of the device. The patient data is displayed on the display in response to the initiation of activation and/or deactivation of the device.

Abstract: A supply of test strips for bodily fluid sampling are provided on a tape such that advancing the tape serves to advance the test strips. One end of the test strips are attached to the tape, and their free end is allowed to extend away from the tape for use. This extension facilitates dosing and reduces the chances for contamination. Prior to use the test strips are maintained in a sealed container and/or under a removable covering to preserve their integrity and improve shelf life.

Abstract: Human or animal body fluids can be measured in-vivo to determine analyte concentrations, such as glucose. The measurement system comprises an exchangeable sensor for in-vivo placement, a data carrier with calibration data for the sensor, a housing having a first chamber for receiving a sterile sensor and a second chamber for receiving a data carrier, and a base station that couples to the housing for transmitting measurement signals to an evaluation unit. Replacement sterile sensors can be packaged in a sterile package and the data carrier associated with the replacement sensor can be packaged in a non-sterile package.

Abstract: An infusion system comprises an infusion unit for infusing fluid into a user's body and a remote control for wirelessly receiving or sending signals to the infusion unit. The infusion system is capable of operating in two separate modes, namely a remote control mode and a direct control mode. In the remote control mode, an infusion command is generated by an input devise of the remote control. The verification to a user that the command has been received, executed or transmitted is outputted by an output device in the remote controller. In the direct control mode the infusion command is generated by an input device of the infusion unit. The verification to a user that the command has been received, executed or transmitted is outputted by an output device in the infusion unit.

Abstract: The invention refers to an injection device for the injection of a medical agent, in particular insulin, comprising: a housing, a reception compartment for a vial containing the agent to be injected, advancement mechanics for moving an injection needle that is inserted in the device in a direction of puncturing, and a pressing facility for pressing agent from a vial that is inserted in the reception compartment for the purpose of an injection process. The advancement mechanics, effects, in a first device function for an injection process, a first motion profile of an inserted injection needle, in which a resting phase follows after an advancement motion, during which resting phase the inserted injection needle for an injection process is at rest with respect to the device housing, and effects, in a second device function for obtaining a body fluid sample for diagnostic purposes, a second motion profile of an inserted injection needle, in which a returning motion follows immediately after a puncturing motion.

Abstract: A control solution packet for calibrating a bodily fluid sampling device includes a container, a control solution pressurized within the container, and a membrane for covering and sealing the container. The control solution can be pressurized before or during calibration so as to ensure the appropriate amount of control solution is delivered to the bodily fluid sampling device. The control solution is manufactured to have a viscosity that controls delivery of the control solution to the device. The membrane is permeable by a piercing device of the bodily fluid sampling device and seals around the piercing device during calibration. In another aspect, the container is in the form of a capsule or dosing attachment that contains the control solution along with a sponge-like material.

Abstract: The present invention provides an integrated measuring device that includes a blood collection system for collecting blood for diagnostic purposes. The blood collection system comprises an electric motor which provides energy for propelling a lancet. The blood collection system comprises a mechanical energy store in which the electric energy that is converted by the motor is stored in the form of mechanical energy. The use of a mechanical energy store allows the use of known mechanical drive elements. The blood collection system can also be electrically activated and is thus easy to use for the operator. The motor can also be coupled to another system component, such as a test strip or lancet drum, to operate it.

Abstract: The invention concerns an analytical instrument for assaying body fluids, the instrument having the following features: a) a housing provided with a receiving element for engaging a body part, b) an abutment for the body part which can be moved between a release position and an operating position relative to the receiving element, c) a lancing unit having a lancing element that can pierce the body part resting against the abutment in a linear lancing stroke, d) a test tape unit having a test tape for receiving body fluid issuing from the body part, and e) a detection unit for examining the body fluid applied to a section of the test tape.

Abstract: The invention generally related to a method and device for displaying the remaining serviceable life of a battery-operated analytical device for analysis of a medically-relevant component of a body fluid, in particular of a blood glucose measuring device.