Methods, apparatus, and systems to non-invasively determine intra-luminal placement and patency of a vascular access device. Patency and/or placement are estimated indirectly by measuring a physiological parameter which is indicative of proper patency and/or placement of the vascular access device in a patient. The measurement is compared to a reference value or calibration. If the comparison indicates indication of proper patency and/or placement, a signal is generated. The signal can be used in a number of ways. One example is to give a user-perceivable alarm or indication of proper patency and/or placement. Non-limiting examples include activating a light, an audible buzzer, a vibration, readable displayed text or graphics, or some combination of the same. The user can then have an indirect and at least semi-automatic way of estimating proper patency and/or placement of a vascular access device.

The present invention provides a sensor garment including a harness. In one exemplary embodiment, the sensor garment includes a textile portion, a device-retention element coupled to the textile portion, and a stretchable harness coupled to the textile portion. The harness includes a conductive element disposed between layers of film. The conductive element includes a first termination point at the device retention element, configured to connect to a monitor device. The conductive element includes a second termination point configured to connect to a sensor or transceiver.

The present invention provides a sensor garment including a harness. In one exemplary embodiment, the sensor garment includes a textile portion, a device-retention element coupled to the textile portion, and a stretchable harness coupled to the textile portion. The harness includes a conductive element disposed between layers of film. The conductive element includes a first termination point at the device retention element, configured to connect to a monitor device. The conductive element includes a second termination point configured to connect to a sensor or transceiver.

An intravascular ultrasound (IVUS) device that includes a flexible elongate member having a proximal portion and a distal portion; a controller coupled to the distal portion of the flexible elongate member; an ultrasound transducer disposed at the distal portion of the flexible elongate member and in communication with the controller; a pressure transducer disposed at the distal portion of the flexible elongate member and in communication with the controller; and plurality of conductors extending from the controller to the proximal portion of the catheter, at least one conductor of the plurality of conductors being configured to carry both the signals representing information captured by the ultrasound transducer and information captured by the pressure transducer.

Sensor circuit device for measuring a bio-potential and/or a bio-impedance of a body, including a master circuit, and at least two active bi-electrodes connected to, and remotely powered by, the master circuit via single-wire first connector. The sensor circuit device further includes a single passive current electrode being connected to the master circuit via single-wire second connector. The sensor circuit device cooperates with a biological signal amplifier configured to measure a bio-potential and/or a bio-impedance. Each active bi-electrode is connectable to the biological signal amplifier via the first connector, such that a bio-potential of the body is measurable between the two active bi-electrodes when the active bi-electrodes and the single current electrode are in contact with a surface of the body.

A noninvasive blood pressure monitor. The noninvasive blood pressure monitor may include an inflatable cuff, a pressure transducer, one or more air pumps, and a processor. The processor may control the air pump(s) so as to initiate inflation of the cuff. The processor may also identify an oscillometric signal in an output of the pressure transducer, and may determine an envelope of the oscillometric signal. The processor may also determine one or more characteristics of the envelope of the oscillometric signal, and may control the air pump(s) so as to stop inflation of the cuff based on the one or more characteristics of the envelope of the oscillometric signal.

An electrode system includes an electrode, a connector, and a cable with an in- line radio-frequency filter module comprising resistors and inductors without any deliberately added capacitance. The resistors are arranged in an alternating series of resistors and inductors, preferably with resistors at both outer ends, and connected electrically in series. The in-line module is located at a specific location along the wire, chosen through computer modeling and real-world testing for minimum transfer of received RF energy to a patient's skin, such as between 100 cm and 150 cm from the electrode end of a 240 centimeter cable. The total resistance of the resistors plus cable, connectors and solder is 1000 ohms or less; while the total inductance is roughly 1560 nanohenries. The inductors do not include ferrite or other magnetic material and are, together with the resistors, stock components thereby simplifying manufacture and reducing cost.

A coupling arrangement for a bio-signal measurement, comprises at least two spring connectors of a bio-signal processing device, and a holder comprising a combination of a wall and a substrate, which form a pocket inside the holder, the wall following an outer contour of the bio-signal processing device. The holder has an aperture for inserting the bio-signal processing device into the pocket and removing the bio-signal processing device from the pocket. The holder includes electric conductor lines, which are in a wired electric contact with electrodes of the substrate, the electrodes receiving at least one bio-signal. The electric conductor lines are attached on the substrate inside the pocket, the electric conductor lines and the at least two spring connectors connecting electrically with each other in response to insertion of the bio-signal processing device in the pocket.

A male sexual function detector and a male sexual function detection system are provided. The male sexual function detector includes a housing, a detection element, a physical stimulation element, a waterproof cable, a bearing, a drive element, and a circuit board. The detection element, the physical stimulation element, the waterproof cable, the bearing, the drive element and the circuit board are disposed within the housing. The detection element includes a pressure sensor or a Doppler sensor. The physical stimulation element allows the bearing to rotate by the drive element, thereby driving the physical stimulation element. The detection element detects the sexual function. A detection signal is received by the circuit board to obtain the detection results. The male sexual function detection system includes a male sexual function detector, an electronic device, and a cloud database. The male sexual function detection system allows a subject to obtain detection results.

A wearable medical device is provided for monitoring a cardiac condition of a patient, where the device is releasably mounted to the patient's chest and includes at least two skin-facing electrodes forming a first one or more ECG leads for ongoing monitoring of heart functioning and at least one touch electrode for intermittently obtaining additional circuit vectors for deriving additional metrics regarding the functioning of the patient's heart. Each touch electrode is configured to form an additional lead/vector that is a larger vector and/or separated by at least 15° from a corresponding first lead/vector formed from the first one or more ECG leads in a vector cardiogram representation of the first one or more ECG leads and the additional lead/vector.