A monitor configuration system which communicates with a physiological sensor, the monitor configuration system including one or more processors and an instrument manager module running on the one or more processors. At least one of the one or more processors communicates with the sensor and calculates at least one physiological parameters responsive to the sensor. The instrument manager controls the calculation, display and/or alarms based upon the physiological parameters. A configuration indicator identifies the configuration profile. In one aspect of the invention, the physiological sensor is a optical sensor that includes at least one light emitting diode and at least one detector.

An electrocardiography patch is provided. A backing has an elongated strip with a midsection connecting two rounded ends. The midsection tapers in from each of the rounded ends and is narrower than each of the two rounded ends. Each electrode, of a pair of electrodes, is positioned on one of the rounded ends of the backing, on a contact surface, to capture electrocardiographic signals. A flex circuit is coupled to each of the electrodes. A non-conductive receptacle is affixed on an outer surface of the backing, opposite the contact surface. Electrical contacts are provided on a surface of the non-conductive receptacle opposite the backing. A battery is provided on the outer surface of the backing and a processor is powered by the battery to write the electrocardiographic signals into memory.

A system, a method, and a computer program product may be provided for providing a remedial procedure. The system comprises a wearable device having sensors to measure health parameters of a user, and processors connected to the wearable device. The processors may receive the health parameters from the sensors, determine a physical wellness value for the user based on the health parameters and predefined physical wellness thresholds, and determine a mental wellness value for the user based on the health parameters and predefined mental wellness thresholds. The processors may identify a risk factor associated with a health of the user based on the physical wellness value and the mental wellness value. The processors may provide a remedial procedure in real-time designed to at least mitigate the identified risk factor.

A system is provided for integrating at least one portable computing device with a resuscitative medical device such as a defibrillator. The system may include a carrying case coupled to the resuscitative medical device. The carrying case may include a storage space for the at least one portable computing device and a wireless charging system for charging the at least one portable computing device. The system may be configured to enable secure data transfer between each of the devices, including data communication and data storage. A processor of the resuscitative medical device may be configured to activate the wireless charging system and charge the at least one portable computing device under certain circumstances. The processor may further be configured to prioritize or optimize charging and data transfer between the resuscitative medical device and each of multiple portable computing devices.

A method for determining system resistance of at least one power supply of a handheld medical device, the method including: a) generating at least one excitation voltage signal, wherein the excitation voltage signal comprises at least one direct current (DC) voltage signal, wherein the excitation voltage signal has a fast transition DC flank of 20 ns or less; b) applying the excitation voltage signal to at least one reference resistor having a predetermined or pre-defined resistance value, wherein the reference resistor is arranged in series with the power supply; c) measuring a response signal of the power supply; d) determining a signal flank from the response signal and determining an ohmic signal portion from one or both of shape and height of the signal flank; and e) determining the system resistance of the power supply from the ohmic signal portion.

Disclosed is a surgical instrument, comprising a shaft, an articulation joint extending distally from the shaft, and an end effector extending distally from the articulation joint. The end effector comprises a jaw, and a staple cartridge seatable in the jaw. The staple cartridge comprises a cartridge body, staples removably stored in the cartridge body, and a first antenna. The surgical instrument further comprises a remote power source configured to supply power, a second antenna configured to cooperate with the first antenna when the staple cartridge is seated in the jaw to transmit at least one of the power and a data signal to the staple cartridge, and a tuning electronics package located in a cavity in a proximal portion of the end effector. The tuning electronics package is configured to facilitate a locally tunable wireless transmission of the at least one of the power and the data signal.

Example implants, systems and methods using sensors for orthopedic surgical assessment and/or planning are described herein. An example system can include a wearable sensor device for pre-operative use by a patient before an orthopedic surgery to generate pre-operative sensor data. The system can also include an implantable sensor device (e.g., a bone implant) to generate and aggregate post-operative sensor data associated with the patient after the surgery. The system can retrieve the pre-operative sensor data and the post-operative sensor data and predict, analyze or assess an outcome of the surgery.

Systems, devices, and methods are provided for changing the power state of a sensor control device in an in vivo analyte monitoring system in various manners, such as through the use of external stimuli (light, magnetics) and RF transmissions.

An electrocardiography patch is provided. A backing includes two rounded ends connected by a middle section that is narrower than the two rounded ends. An electrode is positioned on a contact surface of the backing on each rounded end. A circuit trace is electrically coupled to each of the electrodes. A battery is positioned on an outer surface of the backing, opposite the contact surface, on one of the rounded ends.

An electrocardiography monitor is provided. A sealed housing includes one end wider than an opposite end of the sealed housing. Electronic circuitry is provided within the sealed housing. The electronic circuitry includes an electrographic front end circuit to sense electrocardiographic signals and a micro-controller interfaced to the electrocardiographic front end circuit to sample the electrocardiographic signals. A buzzer within the housing outputs feedback to a wearer of the sealed housing.