Abstract: A gatekeeper electronic signal can be generated by a patient sensor and/or in an intermediate device, such as an electrical cable, that is separate from a patient's physiological information electronic signal. The gatekeeper signal can be generated to indicate to a computer monitor that the sensor and/or cable is of the type that is compatible with, and/or usable with, such computer monitor, and/or that the sensor and/or cable is properly attached to the computer monitor. The gatekeeper signal can be created by an ambient temperature sensor on, or in electrical communication with, the patient monitor, and/or the gatekeeper signal can be created by a gatekeeper electronic signal generator to simulate an ambient temperature value. The gatekeeper signal can be separate from an electronic signal or plurality of signals that include patient physiological information, and the gatekeeper signal may not include any patient physiological information.

Abstract: A patient monitor configured to receive patient-information electrical signals from an invasive patient sensor and a minimally invasive patient sensor, the patient monitor including a base unit and a detachable user interface unit for displaying hemodynamic parameters determined by the base unit. The base unit and user interface unit can be docked together, tethered together through a cabled connection, or physically separated from one another using wireless communication to transmit and receive information. The base unit and the user interface unit may pair before the user interface unit displays data to link the base unit with the user interface unit. The patient monitor can be configured to switch between invasive and minimally invasive monitoring of hemodynamic parameters of a patient, using invasive measurements to calibrate minimally invasive measurements.

Abstract: A patient monitor configured to receive patient-information electrical signals from an invasive patient sensor and a minimally invasive patient sensor, the patient monitor including a base unit and a detachable user interface unit for displaying hemodynamic parameters determined by the base unit. The base unit and user interface unit can be docked together, tethered together through a cabled connection, or physically separated from one another using wireless communication to transmit and receive information. The base unit and the user interface unit may pair before the user interface unit displays data to link the base unit with the user interface unit. The patient monitor can be configured to switch between invasive and minimally invasive monitoring of hemodynamic parameters of a patient, using invasive measurements to calibrate minimally invasive measurements.

Abstract: A gatekeeper electronic signal can be generated by a patient sensor and/or in an intermediate device, such as an electrical cable, that is separate from a patient's physiological information electronic signal. The gatekeeper signal can be generated to indicate to a computer monitor that the sensor and/or cable is of the type that is compatible with, and/or usable with, such computer monitor, and/or that the sensor and/or cable is properly attached to the computer monitor. The gatekeeper signal can be created by an ambient temperature sensor on, or in electrical communication with, the patient monitor, and/or the gatekeeper signal can be created by a gatekeeper electronic signal generator to simulate an ambient temperature value. The gatekeeper signal can be separate from an electronic signal or plurality of signals that include patient physiological information, and the gatekeeper signal may not include any patient physiological information.

Abstract: A gatekeeper electronic signal can be generated by a patient sensor and/or in an intermediate device, such as an electrical cable, that is separate from a patient's physiological information electronic signal. The gatekeeper signal can be generated to indicate to a computer monitor that the sensor and/or cable is of the type that is compatible with, and/or usable with, such computer monitor, and/or that the sensor and/or cable is properly attached to the computer monitor. The gatekeeper signal can be created by an ambient temperature sensor on, or in electrical communication with, the patient monitor, and/or the gatekeeper signal can be created by a gatekeeper electronic signal generator to simulate an ambient temperature value. The gatekeeper signal can be separate from an electronic signal or plurality of signals that include patient physiological information, and the gatekeeper signal may not include any patient physiological information.

Abstract: A patient monitor configured to receive patient-information electrical signals from an invasive patient sensor and a minimally invasive patient sensor, the patient monitor including a base unit and a detachable user interface unit for displaying hemodynamic parameters determined by the base unit. The base unit and user interface unit can be docked together, tethered together through a cabled connection, or physically separated from one another using wireless communication to transmit and receive information. The base unit and the user interface unit may pair before the user interface unit displays data to link the base unit with the user interface unit. The patient monitor can be configured to switch between invasive and minimally invasive monitoring of hemodynamic parameters of a patient, using invasive measurements to calibrate minimally invasive measurements.

Abstract: A thermal interface between a removable cryogenic refrigerator (4) and an article (10) to be cooled by the cryogenic refrigerator. The thermal interface consists of a recondensing chamber filled with a gas (12), the recondensing chamber being in thermal contact with a cooling surface (9) of the refrigerator and the article (10) to be cooled.

Abstract: A gatekeeper electronic signal can be generated by a patient sensor and/or in an intermediate device, such as an electrical cable, that is separate from a patient's physiological information electronic signal. The gatekeeper signal can be generated to indicate to a computer monitor that the sensor and/or cable is of the type that is compatible with, and/or usable with, such computer monitor, and/or that the sensor and/or cable is properly attached to the computer monitor. The gatekeeper signal can be created by an ambient temperature sensor on, or in electrical communication with, the patient monitor, and/or the gatekeeper signal can be created by a gatekeeper electronic signal generator to simulate an ambient temperature value. The gatekeeper signal can be separate from an electronic signal or plurality of signals that include patient physiological information, and the gatekeeper signal may not include any patient physiological information.

Abstract: In order to minimize the loss of cryogen during transportation of superconductive magnet systems, or indeed at any time that the refrigerator is turned off, part of the boil-off gas is directed from the cryogen vessel through the refrigerator interface and past the refrigerator to cool the refrigerator. Some of the heat conducted along the refrigerator into the system is intercepted and removed by that part of the boil-off gas. The heat load onto the cryogenic vessel is thereby reduced, which in turn reduces the boil-off of cryogen from the cryogenic vessel. This part of the boil-off gas is then vented from the system along with the remainder of the boil-off gas, for example to leave the cryogenic liquid vessel via the access neck.

Abstract: A cryogenic magnet system, comprising a cryogenic vessel (1) housing a magnet winding, a vacuum jacket (3) enclosing the cryogenic vessel and a refrigerator (4) at least partially housed within the vacuum jacket and thermally linked (6) to the cryogenic vessel. In particular, the system further comprises an electromagnetic shield.

Abstract: A substantially cylindrical cryostat defining an axial imaging region, the cryostat housing a magnet which, in use, provides a substantially homogeneous magnetic field in the imaging region, further comprising a refrigerator arranged to cool certain elements of the cryostat, said refrigerator comprising a magnetic material which, in use, oscillates along an axis of the refrigerator. The cryostat is arranged such that the axis of the refrigerator is substantially tangential to a circle centred on the axis of the cylindrical cryostat.

Abstract: A cryogenic magnet system, comprising a cryogenic vessel (1) housing a magnet winding, a vacuum jacket (3) enclosing the cryogenic vessel and a refrigerator (4) at least partially housed within the vacuum jacket and thermally linked (6) to the cryogenic vessel. In particular, the system further comprises an electromagnetic shield.

Abstract: A thermal interface between a removable cryogenic refrigerator (4) and an article (10) to be cooled by the cryogenic refrigerator. The thermal interface consists of a recondensing chamber filled with a gas (12), the recondensing chamber being in thermal contact with a cooling surface (9) of the refrigerator and the article (10) to be cooled.

Abstract: In order to minimize the loss of cryogen during transportation of superconductive magnet systems, or indeed at any time that the refrigerator is turned off, part of the boil-off gas is directed from the cryogen vessel through the refrigerator interface and past the refrigerator to cool the refrigerator. Some of the heat conducted along the refrigerator into the system is intercepted and removed by that part of the boil-off gas. The heat load onto the cryogenic vessel is thereby reduced, which in turn reduces the boil-off of cryogen from the cryogenic vessel. This part of the boil-off gas is then vented from the system along with the remainder of the boil-off gas, for example to leave the cryogenic liquid vessel via the access neck.

Abstract: The present invention relates to oral care compositions, especially toothpastes, comprising: a safe and effective amount of phosphopeptide-amorphous calcium phosphate complex (“PP-ACP”); a safe and effective amount of a fluoride ion source; a safe and effective amount of a phosphate buffer; a pharmaceutically-acceptable topical, oral carrier; wherein the pH of the final composition is greater than 8 to about 12 and the composition has improved fluoride stability.