Abstract: A device for clamping attachment to a body part is provided. The device includes a sensor element, a first clamping element and a second clamping element. The device is adapted to receive the body part between the first clamping element and the second clamping element. The first clamping element includes a first deformable side wall and a second deformable side wall, which form a profile of the first clamping element along a longitudinal axis of the first clamping element. The first clamping element further includes a number of first connecting elements extending between and connecting the first side wall and the second side wall, so that the first clamping element is deformable such that the first clamping element bends towards the body part when applied to the body part.

Abstract: A clamping device and a sensor cable with such a clamping device. The clamping device includes a holding element (30) with a holding surface (31), and a counter-holding element (40) with a counter-holding surface (41). The holding surface (31) and the counter-holding surface (41) are arranged to clampingly receive the electrical contact (20) therebetween. The holding element (30) is elastically deformable by actuation with an actuating force (F, F2) in such a way that a position of the holding surface (31) relative to the counter-holding surface (41) is variable between a first position (p1) for clamping reception of the electrical contact (20) and a second position (p2) for release of the electrical contact (20).

Abstract: An oxygen saturation sensor includes a textile basic structure extending in a direction of a longitudinal axis. The basic structure has a resiliently variable cross-sectional shape, so that the oxygen saturation sensor can be fixed to a measurement site. The oxygen saturation sensor also includes a light-emitting diode and a radiation detector. The light-emitting diode and the radiation detector are accommodated in or on the basic structure and are thus arranged in a cross-sectional plane of the basic structure.

Abstract: A ventilation tube unit (2), for connection to a medical ventilator, includes an outer tube (4) with a tubular connection device (18) with a jacket-side branch (24, 28), for connecting a medical unit such as a water trap, arranged between a first outer tube part (20) and a second outer tube part (22). An inner line (6) is arranged within and extends with the outer tube (4) between two port connectors (8). Each outer tube part (20, 22) includes a variable-length outer tube part that can be varied between a compressed state and an expanded state. The connection device (18) is displaceable in the longitudinal direction (A) relative to the inner line (6) by a compression of one outer tube part (20) and a corresponding expansion of the other outer tube part (22). A ventilation system with at least one such ventilation tube unit is also provided.

Abstract: A double temperature sensor determines the body core temperature of a living being. The double temperature sensor includes a sensor block (2), which on one side carries a first temperature sensor (4) provided for placing on the skin surface and on the other side carries a second temperature sensor (5) spaced from the first. An evaluating unit calculates the body core temperature using the measured values of the first and second temperature sensors. The sensor block (2) is held in a hood-shaped housing shell (1) which is shaped in such a manner that the first temperature sensor (4) on the sensor block and the peripheral outer edge (8) of the housing shell (1) spaced therefrom lie in one plane. When the housing shell (1) is lying on the skin surface, the sensor block (2) is surrounded by an air-filled cavity closed off by the housing shell.

Abstract: A clamping device (1), for coupling a sensor cable (2) to an electrical contact, has a circumferential, elastically deformable frame (3). The frame has an outer surface (5), an inner surface (6) facing an inner area (4), a first end face (7) and an opposite second end face (8). A contact device (9) is held at the frame and extends into the inner area. A counter-holding device (10), at the frame, has a counter-holding element (11). The contact device and the counter-holding device form a receiving space for holding the electrical contact in a holding position. A relative movement into a first released position is brought about by a pressing on both sides from the outside against the outer surface on a first frame axis (12). A second released position is provided by pressing on both sides against the frame outer surface on a second frame axis (13).

Abstract: A blood pressure cuff (10), for determining the blood pressure in newborns, includes a chamber section (20) with an air chamber (22) and a handling section (30) for placing and fastening the chamber section (20) around an arm (100) of a newborn. The air chamber (22) has a chamber wall (24), which has, along a circumferential direction (U) of the air chamber (22), a longitudinal sealing seam (40). Two longitudinal edges (26a, 26b) of the chamber wall (24) are connected to one another overlappingly opposite each other in an airtight manner by the longitudinal sealing seam (40).

Abstract: A glass fiber mat comprises glass fibers of a first kind, glass fibers of a second kind and a binding agent. Glass fibers of the first kind in this case are characterized by a mean fiber diameter of under 6 ?m and compliance with the EC Protocol “ECB/TM/27 rev. 7” and glass fibers of the second kind by a mean fiber diameter of over 6 ?m. The ratio between the weight component of glass fibers of the first kind and the weight component of glass fibers of the second kind is between 0.01 and 0.15. And the surface weight of the glass fiber mat is between 25 g/m2 and 80 g/m2. In a CV floor covering comprising a usable layer and a structural layer, the structural layer comprises a glass fiber mat of this kind provided with impregnation.

Abstract: A measuring device (10) has at least one sensor (16, 18), which can be applied to the skin surface (12) of a patient for detecting a measured value with the sensor (16, 18). The device (10) has two contact surfaces (20, 22) on an underside (24), which is intended for being in contact with the skin surface (12) of the patient. A current detecting (32, 34), detects a measuring current (30) resulting from a particular effective electric resistance between the contact surfaces (20, 22). A method for operating such a measuring device (10) and a system with such a measuring device (10) are also provided.

Abstract: A second part extending around a first part in a plugged-together state. The second part has snap-in element with an inwardly protruding projection for meshing with a complementary recess on an outer surface of the first part to hold the second part fixed in the axial direction on the first part. Both parts have a central passage opening. One part has an end area expanding towards the outlet opening in a connection area, and the other part is connected to an elastic section, arranged in its interior. The front end of the elastic section is pressed into contact with the expanded end area of the opposite part. The projection of the snap-in element maintains the first and second parts meshed together, so that the elastic section exerts a sealing function due to the pressure on the expanding end area.

Abstract: A medical sensor extension cable includes a sensor electrical contacting interface, that receives an electrical sensor signal which indicates a physiological parameter of a patient, and a wired data interface, that connects to a data network device. An integrated circuit determines measured values of the physiological parameter based on the sensor signal, to provide an alarm limit value, to establish a presence of an alarm event as a function of a comparison of the measured values and the at least one alarm limit value, as well as to provide data elements, which indicate the measured values and the presence of the alarm event in the event of an alarm, via the data interface. A data network device includes a data connection interface for a data interface of the extension cable. A display interface provides a display signal, which indicates the measured values and the alarm limits.

Abstract: A blood pressure cuff (10), for determining the blood pressure in newborns, includes a chamber section (20) with an air chamber (22) and a handling section (30) for placing and fastening the chamber section (20) around an arm (100) of a newborn. The air chamber (22) has a chamber wall (24), which has, along a circumferential direction (U) of the air chamber (22), a longitudinal sealing seam (40). Two longitudinal edges (26a, 26b) of the chamber wall (24) are connected to one another overlappingly opposite each other in an airtight manner by the longitudinal sealing seam (40).

Abstract: A measuring device (10) has at least one sensor (16, 18), which can be applied to the skin surface (12) of a patient for detecting a measured value with the sensor (16, 18). The device (10) has two contact surfaces (20, 22) on an underside (24), which is intended for being in contact with the skin surface (12) of the patient. A current detecting (32, 34), detects a measuring current (30) resulting from a particular effective electric resistance between the contact surfaces (20, 22). A method for operating such a measuring device (10) and a system with such a measuring device (10) are also provided.

Abstract: A glass fibre mat comprises glass fibres of a first kind, glass fibres of a second kind and a binding agent. Glass fibres of the first kind in this case are characterized by a mean fibre diameter of under 6 ?m and compliance with the EC Protocol “ECB/TM/27 rev. 7” and glass fibres of the second kind by a mean fibre diameter of over 6 ?m. The ratio between the weight component of glass fibres of the first kind and the weight component of glass fibres of the second kind is between 0.01 and 0.15. And the surface weight of the glass fibre mat is between 25 g/m2 and 80 g/m2. In a CV floor covering comprising a usable layer and a structural layer, the structural layer comprises a glass fibre mat of this kind provided with impregnation.

Abstract: A ventilation tube unit (2), for connection to a medical ventilator, includes an outer tube (4) with a tubular connection device (18) with a jacket-side branch (24, 28), for connecting a medical unit such as a water trap, arranged between a first outer tube part (20) and a second outer tube part (22). An inner line (6) is arranged within and extends with the outer tube (4) between two port connectors (8). Each outer tube part (20, 22) includes a variable-length outer tube part that can be varied between a compressed state and an expanded state. The connection device (18) is displaceable in the longitudinal direction (A) relative to the inner line (6) by a compression of one outer tube part (20) and a corresponding expansion of the other outer tube part (22). A ventilation system with at least one such ventilation tube unit is also provided.

Abstract: A double temperature sensor determines the body core temperature of a living being. The double temperature sensor includes a sensor block (2), which on one side carries a first temperature sensor (4) provided for placing on the skin surface and on the other side carries a second temperature sensor (5) spaced from the first. An evaluating unit calculates the body core temperature using the measured values of the first and second temperature sensors. The sensor block (2) is held in a hood-shaped housing shell (1) which is shaped in such a manner that the first temperature sensor (4) on the sensor block and the peripheral outer edge (8) of the housing shell (1) spaced therefrom lie in one plane. When the housing shell (1) is lying on the skin surface, the sensor block (2) is surrounded by an air-filled cavity closed off by the housing shell.

Abstract: A double temperature sensor is provided for determining the body temperature. The sensor includes at least a first temperature sensor element for measuring a near-surface temperature of the ambient air and a second temperature sensor element for measuring a temperature of the skin surface. The first and the second temperature sensor elements are arranged in a sensor block. A holding element surrounds the sensor block at least partially. An adhesive element fixes the holding element on the skin surface. A spring element acts on the sensor block and provides a spring force directed in the direction of the skin surface.

Abstract: A glass fibre mat comprises glass fibres of a first kind, glass fibres of a second kind and a binding agent. Glass fibres of the first kind in this case are characterized by a mean fibre diameter of under 6 ?m and compliance with the EC Protocol “ECB/TM/27 rev. 7” and glass fibres of the second kind by a mean fibre diameter of over 6 ?m. The ratio between the weight component of glass fibres of the first kind and the weight component of glass fibres of the second kind is between 0.01 and 0.15. And the surface weight of the glass fibre mat is between 25 g/m2 and 80 g/m2. In a CV floor covering comprising a usable layer and a structural layer, the structural layer comprises a glass fibre mat of this kind provided with impregnation.

Abstract: A medical electrode is provided for detecting and transmitting electric pulses from the body surface of a patient to an electric pulse processor. The medical electrode includes an outer carrier and at least one inner carrier (3, 3?, 3?). The outer carrier and the inner carrier are connected at a defined number of geometrically distributed points (2). The points (2) form an outer edge (4) of the inner carrier and are perforated, so that the outer carrier and the inner carrier can be separated at these points (2). An adhesion area (5) is formed on the underside of the outer carrier (1) and of the inner carrier for adhering the medical electrode to the patient body surface. A contact element (7) is provided with a conductive area arranged concentrically to the contact element (7) for establishing contact with the body surface of the patient. The contact element (7) and the conductive area (8) are arranged within the inner carrier.

Abstract: A safety helmet (1) has a circumferential module ring (2), made especially of a thermoplastic plastic. The module ring (2), has a plurality of plug-in slots (3), which are located at spaced locations from one another in the direction of the module ring (2). This provides standardized simultaneous mounting possibilities for various functional accessories with plug elements complementary to the plug-in slots (3).