Abstract: A system and method are capable of ensuring that one or more text strings will be able to be fully rendered in a target area of a user interface or a target area of a graphics file. The system and method determine the number of pixels of first and second reference text that fit in the target area in the horizontal direction and the vertical direction, respectively, determine the number of pixels of string text in the horizontal direction and the vertical direction, and compare the number of pixels in the horizontal direction of the first reference text and the vertical direction of the second reference text respectively to the number of pixels in the horizontal direction and the vertical direction of the text string that is desired to be rendered in the target area to determine whether the text string will fit in the target area.

Abstract: Devices and methods for executing a customizable configuration for displaying one or more physiological parameters of a patient are disclosed. The device includes a display configured to display information related to the patient including physiological data. The device provides a graphical user interface (GUI) on the display including a locked sub-area and a scrollable sub-area, respectively, to display measured values of the physiological parameters. Upon receipt of an input, the device allows the measured values of the physiological parameters to be further configured between the locked sub-area and the scrollable sub-area.

Abstract: A supply system (1a) includes a basic body (2) and at least one supply port (3 through 8), which is flush-mounted in the basic body (2) and provides a supply medium. The basic body (2) extends along a longitudinal axis and includes a plurality of outer wall sections (9 through 12) and at least one connection section (13 through 16). The connection section or each connection section (13 through 16) mechanically connects to one another two outer wall sections (9 through 12), which are adjacent to one another. At least one connection section (13 through 16) has at least one undercut (17 through 24). The undercut or each undercut (17 through 24) has the form of a channel or flute or groove or sectional rail and extends along the longitudinal axis of the basic body (2).

Abstract: An automatic power on apparatus, system, method, and circuit automatically control the on/off state of a first electronic device or a second electronic device. When the second electronic device is positioned on, in, or proximate to the mounting area of the first electronic device, the automatic power on circuit establishes a coupling signal between a first portion of the automatic power on circuit and a second portion of the automatic power on circuit, activates the automatic power on circuit based on the coupling signal, and automatically controls an on/off state of the first electronic device or the second electronic device based on the activation of the automatic power on circuit.

Abstract: A protective device (10, 10?) provides a protective cover for a part (12, 12?, 12?) of a medical device and includes a flexible part (14, 14?) and a rigid part (16, 16?). The rigid part (16, 16?) has at least one locking element (28, 28?). The locking element (28, 28?) is lockingly connectable to a counterpiece of the corresponding part (12, 12?, 12?) of the medical device.

Abstract: A system, medical devices, network components, devices, processes and computer programs for medical devices and for network components are provided. The process (10) for a first medical device (400; 400b) for the use of a license-based system function of a network component (500) in a network (600) includes a transmission (11) of a request for an available license into the network (600) and a reception (12) of a reply from a second medical device. The reply indicates that a license for the system function is available at the second medical device. The process includes a request (13) for the available license from the second medical device and reception (14) of information on the available license from the second medical device. The process provides the system function based on the information on the license from the second medical device (400; 400a).

Abstract: A system includes a rigid housing and flexible tubes. The rigid housing includes cable receptacles. Each cable receptacle has a distal end and a longitudinal opening configured to accept a cable. The flexible tubes are configured to accept cables and orient the cables in a customizable, organized manner. Each flexible tube is secured to a respective cable receptacle at the distal end and has a longitudinal opening oriented to align with the longitudinal opening of the respective cable receptacle. Another system includes a vertical stand structure configured to maneuver about a floor and a deformable trough secured to the vertical stand structure. The deformable trough is configured to initially bend in a customizable manner to form a customized configuration and subsequently maintain the customized configuration to facilitate placement of the cables within the deformable trough and provide for mobility of the vertical stand structure.

Abstract: A connector detection system includes a connector interface including a connector port having an interior volume configured receive a connector of a cable; and an optical sensor. The optical sensor includes a transmitter configured to transmit a light beam across the interior volume; a receiver configured to monitor for a reflected light beam corresponding to the transmitted light beam; and processing circuitry configured to determine whether the connector is inserted into the interior volume based on a monitoring for the reflected light beam.

Abstract: A collecting unit, which receives secretion from a patient. The collecting unit comprises a cover (2) and a bag (3), which is mechanically connected to the cover (2). The bag (3) can be converted from a folded state, in which a portion of the bag (3) is folded about a fold axis (FA), into an unfolded state. Two overlapping overlap areas (3.1, 3.2) of the bag (3) that have each a connection area (VB.1, VB.2), are formed in the folded state. These connection areas (VB.1, VB.2) are detachably connected to one another, and preferably in a positively connected. The fold axis (FA) forms a common edge of the two overlap areas (3.1, 3.2).

Abstract: Systems, methods, devices, and connectors are described herein for a modular patient monitoring medical device. A new generation of physiological measurement devices, such as Intelligent Patient Front End Devices (IPFE) can provide updated algorithms, features, and software updates for parameter measurement devices without corresponding releases of a new version of host monitor software. IPFEs, together with patient sensors, comprise a complete physiological patient parameter measurement delivery system. A number and a type of parameter measurement devices can be configured to meet varied and changing clinical needs. Remote access to versions, logs, self-tests, settings, history, and/or measurements via the Internet to one or more parameter measurement devices can provide a unified service approach. The connector is configured to electrically connect any two or more devices and provides an electrical connection that can be simply physically or tactually confirmed.

Abstract: A monitor mount is configured to detachably secure a monitor via a coupling which can be disengaged with an actuator. The monitor mount may be configured to detachably secure the monitor to a support structure via a clip. The monitor may have a reversible cover. The monitor may have a simplified back portion. The simplified back portion may omit couplings or electrical connections such that a back surface of the monitor is continuous. A rack is configured to detachably secure a module therein in multiple positions in which the module is mechanically connected to the rack and electrically connected or disconnected to the rack. The monitor may be a patient monitor and the module may be a patient monitoring module.

Abstract: An apparatus and method of calibrating the apparatus are disclosed. The apparatus may include a scale platform, a warming therapy device comprising a bassinet and at least one electrical device, the warming therapy device being disposed on the scale platform, the scale platform disposed between the warming therapy device and the base; and a conductor assembly adapted to (a) supply electrical power between a power supply and at least some of the at least one electrical device, and (b) enable the transmission of electrical signals from the at least one electrical device to the computer system, the conductor assembly comprising a scale platform cable assembly comprising a plurality of conductors, the scale platform cable assembly having a first connector end and a second connector end, the first connector end being rigidly affixed to the load cell carrier and the second connector end being rigidly affixed to the scale platform cover.

Abstract: A monitor mount is configured to detachably secure a first monitor and/or a second monitor individually or concurrently. The first monitor and the second monitor may have different sizes. Any of the monitors may be a patient monitor.

Abstract: A patient module (20) is intended for use together with a pressure source (12). The patient module (20) couples the pressure source (12) for flow to a patient interface (14) that can be connected to the airways of a patient. The patient module (20) includes at least one valve device (30), which can be controlled by means of a piezo pump, which acts as a valve drive (34) and can preferably be operated at a high frequency. The at least one valve device (30) acts as an exhalation valve (28).

Abstract: A mount configured to dock an electronic device, such as a patient monitor, and to broadcast location information thereto. The mount includes a receptacle to removably dock the electronic device. A communication interface only capable of broadcasting signals is utilized to broadcast a signal indicative of a location where the mount is located a limited distance. The mount is not configured for network connectivity and is for use in areas where wired connectivity is not available such as emergency rooms, transport beds, low acuity units and ambulances.

Abstract: A measurement system (100) determines gas concentrations in a gas mixture of a gas sample by utilizing thermal conductivities and paramagnetic effects of thermal conductivities in the gas mixture involving data sets (203). A circuit arrangement provides measured values with an AC signal component and with a DC signal component to a calculation and control unit (200). An oxygen concentration in the gas mixture of the gas sample is determined based on the standardized AC signal components and a concentration of another gas in the gas mixture of the gas sample is determined based on the standardized DC voltage signal components. Output signals are generated by the calculation and control unit, which indicate the determined oxygen concentration and the determined concentration of another gas in the gas mixture of the gas sample.

Abstract: An automatic power on apparatus, system, method, and circuit automatically control the on/off state of a first electronic device or a second electronic device. When the second electronic device is positioned on, in, or proximate to the mounting area of the first electronic device, the automatic power on circuit establishes a coupling signal between a first portion of the automatic power on circuit and a second portion of the automatic power on circuit, activates the automatic power on circuit based on the coupling signal, and automatically controls an on/off state of the first electronic device or the second electronic device based on the activation of the automatic power on circuit.

Abstract: An HME device, used in a closed breathing circuit of a ventilation system, has a housing with an inlet opening and with an outlet opening, an HME chamber (50a; 50b; 50c; 50d; 50e; 50f; 50g; 50h; 50i) arranged between the inlet opening and the outlet opening for receiving an HME medium and a switching mechanism (70a; 70b; 70c; 70d; 70e; 70f; 70g; 70h; 70i). The HME device can be switched over between an HME mode (M1), in which an HME fluid passage is provided from the inlet opening through the HME chamber to the outlet opening, and a bypass mode (M2), in which a fluid bypass passage is provided from the inlet opening past the HME chamber through a bypass channel (80a; 80b; 80d; 80e; 80f; 80h) in the housing to the outlet opening. The bypass channel is blocked with respect to the HME chamber in the bypass mode (M2).

Abstract: Systems and methods for identifying one or more P-waves in real-time are disclosed. Exemplary implementations may: receive a plurality of signals from an ECG lead configured to be connected with a patient; determine a noise level of the plurality of signals during a pre-determined time interval; identify a plurality of QRS-complex candidates from the received plurality of signals; extract one or more features from each QRS-complex candidate based on the determined noise level of the plurality of signals; cluster, based on the extracted one or more features from each QRS-complex candidate, the plurality of QRS-complex candidates; and identify one or more P-waves from the clustered plurality of QRS-complex candidates. Based on the identified one or more P-waves, a heart block event can be detected.

Abstract: A flow tube (10) has a housing (12, 14) including at least a first housing half (12) and a second housing half (14). Each housing half (12, 14) has a connection surface (20, 22) intended for combination with the other housing half (12, 14). The connection surfaces (20, 22) enclose a mounting gap (30) for an orifice element (16). Outside of the mounting gap (30) the connection surfaces (20, 22) butt against each other in some sections by respective abutting surface portions (32, 34), and outside of the mounting gap (30) and outside of the abutting surface portions (32, 34) the housing halves (12, 14) are integrally combined with each other. A method is provided for producing the flow tube, namely for integrally joining the housing halves (12, 14).