Abstract: A ventilator system for providing respiratory support in cases of acute respiratory failure or severe trauma is described. The ventilator system comprises a ventilator and a tubing system. The system is characterized in that the ventilator comprises a continuous bleed valve configured to be open to air flow from the blower at all times when the blower is operating during both inspiration and expiration; thereby providing a minimal amount of pressure within a patient's lungs at the end of each exhalation—positive end expiratory pressure (PEEP). In an embodiment of the invention the system comprises a manifold block configured to hold the main operating elements of ventilator.

Abstract: A ventilator system for providing respiratory support in cases of acute respiratory failure or severe trauma is described. The ventilator system has a ventilator and a tubing system. The system is characterized in that the ventilator has a continuous bleed valve configured to be open to air flow from the blower at all times when the blower is operating during both inspiration and expiration; thereby providing a minimal amount of pressure within a patient's lungs at the end of each exhalation—positive end expiratory pressure (PEEP). In an embodiment of the invention the system comprises a manifold block configured to hold the main operating elements of the ventilator.

Abstract: Disclosed is a system that includes both an Airway and Ventilation device (AV) and an Automated External Defibrillator (AED) device. The system is provided with components for assisting only minimally trained persons to operate it in emergency situations involving respiratory failure and/or cardiac arrhythmias. The system includes one or both of a mask for applying non-invasive ventilation and a ventilation tube for applying invasive ventilation.

Abstract: Disclosed is a system that comprises both an Airway and Ventilation device (AV) and an Automated External Defibrillator (AED) device. The system is provided with means for assisting only minimally trained persons to operate it in emergency situations involving respiratory failure and/or cardiac arrhythmias.

Abstract: A system for providing decision-assisted critical care to a patient in medical emergency situations in an out of hospital setting includes: a ventilator; an Automated External Defibrillator that includes primary electrocardiogram (ECG) sensors configured as chest pads that can be connected to the chest of the patient and to sense ECG and to deliver an electric shock to the patient's heart; at least one secondary ECG sensor connected at a location other than the chest configured to sense ECG but not to deliver electric shock; and a controller configured, upon detection of shockable cardiac arrhythmias by at least one of said at least one secondary ECG sensors, to (a) instruct a caregiver to place the chest pads on the chest of the patient and to activate the AED, or (b) to automatically activate the AED if the chest pads are already in place on the chest of the patient.

Abstract: An implantable orthopedic device. The device includes: a proximal anchor, configured to be implanted inside a first metatarsal; the anchor having a collar larger than the opening in a metatarsal in which the proximal anchor is implanted; the collar preventing cable to bone contact; a distal anchor, configured to be implanted inside a second metatarsal, adjacent to the first metatarsal; the distal anchor having a male thread, a nut threadable onto the male thread of the distal anchor, and a cord mechanically interconnecting the proximal and distal anchors. A shock absorber includes an elongate housing threadedly positioned within the anchor; the shock absorber accommodates a cord holder mechanically connected to the housing via a damping member, the cord holder is freely rotatable within the housing to prevent the cord from twist kinking when the housing is rotated to adjust a tension force.

Abstract: A system that includes both an Airway and Ventilation device (AV) and an Automated External Defibrillator (AED) device is described. The system allows minimally trained persons to operate it in emergency situations involving respiratory failure and/or cardiac arrhythmias. An integral part of the AV of the system is a face mask manufactured in two parts: a face attachment unit configured to attach to the patient's face and a mask body that is releasably connected to the face attachment unit by a quick release mechanism allowing quick removal of the mask body from the face attachment unit, leaving only the face attachment unit attached to the patients' face, in order to address urgencies such as vomiting. After vomiting ceases and is cleared, then the mask body may be reattached to continue ventilation.

Abstract: A ventilator system for providing respiratory support in cases of acute respiratory failure or severe trauma is described. The ventilator system comprises a ventilator and a tubing system. The system is characterized in that the ventilator comprises a continuous bleed valve configured to be open to air flow from the blower at all times when the blower is operating during both inspiration and expiration; thereby providing a minimal amount of pressure within a patient's lungs at the end of each exhalation positive end expiratory pressure (PEEP). In an embodiment of the invention the system comprises a manifold block configured to hold the main operating elements of ventilator.

Abstract: The invention is a system for providing decision-assisted critical care to a patient in medical emergency situations in an out of hospital setting. The system comprises: a ventilator comprising a pressure generator and oxygen/air delivery means; an Automated External Defibrillator (AED) comprising a battery and primary electrocardiogram (ECG) sensors configured as chest pads that are configured to be connected to the chest of the patient and to both sense ECG and to deliver an electric shock to the patient's heart; at least one secondary ECG sensor configured to sense ECG but not to deliver electric shock and to be connected to the body of the patient at a location other than the chest; and a controller, configured to activate or instruct a caregiver to activate, the AED and to place the chest pads on the chest of the patient upon detection of shockable cardiac arrhythmias by at least one of the at least one secondary ECG sensors.

Abstract: An implantable orthopedic device. The device includes: a proximal anchor, configured to be implanted inside a first metatarsal; the anchor having a collar larger than the opening in a metatarsal in which the proximal anchor is implanted; the collar preventing cable to bone contact; a distal anchor, configured to be implanted inside a second metatarsal, adjacent to the first metatarsal; the distal anchor having a male thread, a nut threadable onto the male thread of the distal anchor, and a cord mechanically interconnecting the proximal and distal anchors. A shock absorber includes an elongate housing threadedly positioned within the anchor; the shock absorber accommodates a cord holder mechanically connected to the housing via a damping member, the cord holder is freely rotatable within the housing to prevent the cord from twist kinking when the housing is rotated to adjust a tension force.

Abstract: An implantable orthopedic device. The device includes: a proximal anchor, configured to be implanted inside a first metatarsal; the anchor having a collar larger than the opening in a metatarsal in which the proximal anchor is implanted; the collar preventing cable to bone contact; a distal anchor, configured to be implanted inside a second metatarsal, adjacent to the first metatarsal; the distal anchor having a male thread, a nut threadable onto the male thread of the distal anchor, and a cord mechanically interconnecting the proximal and distal anchors. A shock absorber includes an elongate housing threadedly positioned within the anchor; the shock absorber accommodates a cord holder mechanically connected to the housing via a damping member, the cord holder is freely rotatable within the housing to prevent the cord from twist kinking when the housing is rotated to adjust a tension force.

Abstract: The invention is a system that comprises both an Airway and Ventilation device (AV) and an Automated External Defibrillator (AED) device. The system is provided with means for assisting only minimally trained persons to operate it in emergency situations involving respiratory failure and/or cardiac arrhythmias. An integral part of AV of the system is a face mask comprised of two parts—a face attachment unit configured to attach to the patient's face and a mask body that is releasably connected to the face attachment unit by a quick release mechanism allowing quick removal of the mask body from the face attachment unit, leaving only the face attachment unit attached to the patients' face, in order to address urgencies such as vomiting. After vomiting ceases and is cleared, then the mask body may be reattached to continue ventilation.

Abstract: An expandable mold configured to be arthroscopically introduced into a joint for in-situ formation of a joint replacement prosthesis, and a flowable, curable substance configured for forming the joint replacement prosthesis inside said mold. In addition, a surgical kit for arthroscopic, in-situ formation of a joint replacement prosthesis, the surgical kit comprising: an expandable prosthesis mold configured to be arthroscopically introduced into a joint; at least one arthroscopic instrument configured to form an ellipsoidal cavity between two interfacing bones of the joint, for receiving said mold; and a first flowable, curable substance configured for forming the prosthesis inside said mold.

Abstract: Multi layer endotracheal tube apparatus (800) comprising an outer flexible elongated tube layer (802) having a proximal end (816) and a distal end (818), defining an inner surface (820) therebetween, at least one flexible elongated inner tube layer (804) having a proximal end (822) and a distal end (824), defining an inner surface (828), the distal end (824) of the inner tube layer (804) defining a distal port section (830), the inner tube layer (804) extending along inner length of the outer tube layer (802), the distal end (824) of the inner tube layer (804) detachably coupled along a closed circumference of the inner surface (820) of the outer tube layer (802), and at least one closure mechanism (806) operative to close the distal port section (830), and detach the distal end (824) of the inner tube layer (804) from the inner surface (820) of the outer tube layer.

Abstract: Determining functional residual lung capacity (FRC) by changing a subject's inspirium FiO2 by a predetermined amount, and a) for each breath in a series of breaths subsequent to changing the FiO2, determining expiratory tidal volume, determining expiratory fractional N2 tidal volume, multiplying the expiratory tidal volume by an absolute difference between the expiratory fractional N2 tidal volume of the breath and that of an immediately preceding breath for a first multiplication result, dividing the first multiplication result by the sum of the differences for a first division result, and multiplying the fractional N2 tidal volume by the sum of the first division results of the breaths for a second multiplication result, and b) dividing the sum of the second multiplication results of the breaths by the absolute difference between the fractional N2 tidal volume of the first and last breaths to produce a measurement of the subject's FRC.

Abstract: A surgical fastening device for pinning a surgical filament to a body tissue. The device includes a grasping handle and a slender shaft extending from the grasping handle. A compartment contains one or more surgical fasteners. An ejecting mechanism is used to eject a surgical fastener from a compartment containing one or more surgical fasteners. The device also includes a filament dispensing system that dispenses surgical filament along the shaft so that a fastener grasps the filament when being ejected from the shaft. The invention also provides surgical fasteners and surgical filaments for use in the device.

Abstract: A respiratory tract differential-pressure flow sensor, including a tube having a distal end that is insertable into a respiratory tract, an interfering body disposed within the tube proximal to the distal end and having a first edge facing one end of the tube and a second edge facing away from the end, the interfering body extending across the diameter of the tube, a first pressure sensing port operative to sense an air pressure, the first port being disposed in the first edge not abutting the wall of the tube, and a second pressure sensing port operative to sense an air pressure, the second port being disposed in the second edge not abutting the wall of the tube, where either of the edges is inclined inwardly towards the axis of the interfering body extending across the diameter of the tube.

Abstract: A respiratory tract differential-pressure flow sensor, including a tube having a distal end that is insertable into a respiratory tract, an interfering body disposed within the tube proximal to the distal end and having a first edge facing one end of the tube and a second edge facing away from the end, the interfering body extending across the diameter of the tube, a first pressure sensing port operative to sense an air pressure, the first port being disposed in the first edge not abutting the wall of the tube, and a second pressure sensing port operative to sense an air pressure, the second port being disposed in the second edge not abutting the wall of the tube, where either of the edges is inclined inwardly towards the axis of the interfering body extending across the diameter of the tube.