Abstract: An electronic apparatus capable of reducing SAR and, simultaneously, suppressing degradation of antenna efficiency is provided. To that end, an electronic apparatus includes a first temple to be positioned on one side of the user's head when the electronic apparatus is worn on the user's head, a second temple to be positioned on the other side of the user's head when the electronic apparatus is worn on the user's head, an first antenna formed in the first temple, an second antenna formed in the second temple, and a transceiver circuit for supplying power to the first antenna and the second antenna.

Abstract: An apparatus and method is related to providing sensing functions that are similar to “human touch” when located in a prosthetic device such as a BION microstimulator that is implanted in a patient. The apparatus includes a power circuit, a communication circuit and a sensor circuit. The power circuit provides power to the communication circuit and the sensor circuit. The sensor cooperates with the communication circuit, which communicates to the brain. The sensor uses various techniques to detect changes in the environment for the surrounding tissue using criteria such as reflectivity, impedance, conductivity, return signal spectrum, return signal rate and return signal phase to name a few. For example, the impedance observed by the sensor changes when: the skin tissue is deformed around the sensor, or when the skin is surrounded by water. The sensory information is interpreted by the brain as an analog of touch or feel.

Abstract: Chemiluminescent detection systems, kits, and microfluidics devices containing same, as well as methods of production and use thereof, are disclosed.

Abstract: Provided according to embodiments of the present invention are methods of monitoring individuals that include securing a photoplethysmograph probe to at least one of a pre-auricular region and a post-auricular region of the individual and obtaining photoplethysmography signals from the photoplethysmography probe. Photoplethysmography probes and helmets related to such methods are also described herein.

Abstract: A device comprises an indicating unit configured to indicate information and a connecting unit configured to connect the indicating unit to an electrode operable to sense an EEG signal, such that the information is indicated at a position at which the electrode is placed. The electrode includes a circuit board and an indicating unit, such as an LED, encased in a water-proof housing.

Abstract: This document discusses, among other things, a modular antitachyarrhythmia therapy system. In an example, a modular antitachyarrhythmia system includes at least two separate modules that coordinate delivery an antitachyarrhythmia therapy, such as defibrillation therapy. In another example, a modular antitachyarrhythmia therapy system includes a sensing module, an analysis module, and a therapy module.

Abstract: Provided are a system and method for generating a pseudo electrogram. The system for generating the pseudo electrogram includes a unipolar electrogram generation unit which generates a unipolar electrogram according to an action potential calculated from an electric physiological model of the heart using a pseudo electrode in which a cross-sectional area is adjusted, and a pseudo electrogram generation unit which generates a pseudo electrogram using the unipolar electrogram.

Abstract: Embodiments include determining a reference value on a first device; broadcasting the reference value from the first device; connecting the first device to a second device if the second device requests data from the first device; transmitting any new data if the second device requests data from the first device; generating and broadcasting a new reference value if the first device has new data; broadcasting the reference value from the first device again if the first device does not have new data; receiving a reference value in the second device from the first device; and if the received reference value does not match the stored reference value then transmitting a request from the second device for new data from the first device, receiving new data from the first device into the second device, and storing the received reference value as a new stored reference value. Numerous other aspects are provided.

Abstract: Systems and methods of scheduling and sending notifications to, and receiving acknowledgements from, patients regarding specific health care events, such as the taking of medications at scheduled times and in prescribed dosages. By directing a patient to take their prescribed dosages of medication at scheduled times based on a schedule of medications prepared for the patient by a health care provider, a caregiver, etc., and enabling the patient to provide acknowledgements of having taken their prescribed dosages of medication, improved health care outcomes can be achieved. Further, by allowing the patient to receive such directives to take their medication, as well as to send such acknowledgements, using a set top box connected to a television set, a mobile device such as a mobile phone, and/or a patient notification device such as a wireless pendant, desired improvements in health care outcomes can be achieved with an increased level of convenience.

Abstract: A stimulator and a method for the treatment of intractable pain syndromes by electrical stimulation of the spinal cord is disclosed. An example method includes positioning a first pair of implantable electrodes to a dura matter in an epidural space proximate to a subject's spinal cord at predetermined locations, positioning a second pair of implantable electrodes to the dura matter in the epidural space proximate to the subject's spinal cord at predetermined locations, and transmitting signals of first and second frequencies through the first and second pairs of implantable electrodes respectively, so that the signals of the first and second frequencies interfere with each other to produce at least one beat signal proximate to the subject's spinal cord. The at least one beat signal has a frequency within a range of more than 250 Hz to about 15,000 Hz.

Abstract: A modular patient monitor provides a multipurpose, scalable solution for various patient monitoring applications. In an embodiment, a modular patient monitor utilizes multiple wavelength optical sensor and/or acoustic sensor technologies to provide blood constituent monitoring and acoustic respiration monitoring (ARM) at its core, including pulse oximetry parameters and additional blood parameter measurements such as carboxyhemoglobin (HbCO) and methemoglobin (HbMet). Expansion modules provide blood pressure BP, blood glucose, ECG, CO2, depth of sedation and cerebral oximetry to name a few. Aspects of the present disclosure also include a transport dock for providing enhanced portability and functionally to handheld monitors. In an embodiment, the transport dock provides one or more docking interfaces for placing monitoring components in communication with other monitoring components. In an embodiment, the transport dock attaches to the modular patient monitor.

Abstract: The present disclosure provides an antenna structure for use in an implantable medical device. The antenna structure includes a first antenna configured to receive wireless signals within a first frequency band, a second antenna configured to receive wireless signals within a second frequency band lower than the first frequency band, and a common output connector. The first antenna includes a first end and a second, free end opposite the first end. The second antenna is connected to the first antenna at a location between the first and second ends. The common output connector is disposed at the first end of the first antenna, and is electrically coupled to the first and second antennas such that signals received by the first and second antennas are output through the common output connector.

Abstract: An inserter assembly for continuous glucose monitoring with medication delivery capability where the assembly has a deployment button containing a needle deployment mechanism having a sharp held in a pre-release position, a housing body in which the deployment button is movably received within a top end of the housing body, the housing body having a sensor deployment assembly containing a lumen and a sensor disposed within the lumen and extending out of the lumen to a circuit board that is part of the sensor deployment assembly, the sensor deployment assembly matingly connected to the sharp where the sharp extends beyond the sensor deployment assembly and contains the sensor not fixedly attached to the sharp, and a sensor housing releasably received within a lower end of the housing body, the sharp extending into a sensor deployment assembly recess within the sensor housing and directly above a sensor opening in a bottom of the sensor housing.

Abstract: Systems, methods, and apparatuses that provide alerts based on analyte data and acceleration data. An analyte sensor may generate the analyte data. An accelerometer may generate the acceleration data. A transceiver may convert the analyte data into analyte concentration values. The transceiver may convert the acceleration data into activity information. The transceiver may generate an alert based on the analyte concentration values and activity information. The alert may be communicated to a user by a mobile medical application executed on the transceiver and/or a display device (e.g., smartphone) in communication with the transceiver. The mobile medical application may display (e.g., on a display of the display device) a plot or graph of the analyte concentration values and activity information with respect to time.

Abstract: Systems and methods for updating software in a hazard detection system are described herein. Software updates may be received by, stored within, and executed by a hazard detection system, without disturbing the system's ability to monitor for alarm events and sound an alarm in response to a monitored hazard event. The software updates may be received as part of a periodic over-the-air communication with a remote server or as part of a physical connection with a data source such as a computer. The software updates may include several portions of code designed to operate with different processors and/or devices within the hazard detection system. The software updates may also include language specific audio files that can be accessed by the hazard detection system to play back language specific media files via a speaker.

Abstract: A method for controlling a functional component of a transportation vehicle by a medical implant of a user of the transportation vehicle including transmitting a signal, which comprises authentication information and status information, from the medical implant to a control device of the transportation vehicle; receiving the signal; establishing validity or invalidity of the received signal; and providing a control command to the functional component of the transportation vehicle, in the case of established validity, in response to status information that indicates a critical health status of the user.

Abstract: A system and method for measuring vital signs and motion from a patient. The system features: (i) first and second sensors configured to independently generate time-dependent waveforms indicative of one or more contractile properties of the patient's heart; and (ii) at least three motion-detecting sensors positioned on the forearm, upper arm, and another different body location of the patient. Each motion-detecting sensor generates at least one time-dependent motion waveform indicative of motion of the location on the patient's body to which it is affixed. A processing component, worn on the patient's body and featuring a microprocessor, receives the waveforms generated by the different sensors and processes them to determine: (i) a pulse transit time calculated using a time difference between features in two separate time-dependent waveforms, (ii) a blood pressure value calculated from the time difference, and (iii) a motion parameter calculated from at least one motion waveform.

Abstract: A system and method of flagging monitored ECG samples for urgent review by a human expert is described, and includes monitoring an electro-cardiogram (ECG) signal of the patient with an adherent device that includes a plurality of electrodes. Based on the monitored ECG signal, detected rhythm abnormalities in the patient are detected and ECG samples are collected with respect to detected rhythm abnormalities. One or more features are identified with respect to each ECG sample, and the features are utilized to flag ECG samples for urgent review by a human expert.

Abstract: The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.

Abstract: A system and method for pairing a dialysis machine with peripheral devices are disclosed. An example system includes first and second memory devices, a first dialysis machine including a first memory device port configured to be connectable to the first memory device, and a second dialysis machine including a second memory device port configured to be connectable to the second memory device. The system also includes an intermediate data transfer unit including a port configured to connect to the first and the second memory devices to enable data transfer with the respective dialysis machines. The intermediate data transfer unit is configured to receive data from a weight sensor, a blood pressure sensor, or a remote exchange device for a patient and store the data to the first or second memory device to communicate the data to the respective first or second dialysis machine.

Abstract: A dialysis method includes: receiving at least one of blood pressure data from a blood pressure monitor or patient weight data from a weight scale at a dialysis machine at least one of (i) before or (ii) after each treatment performed by the dialysis machine; generating ultrafiltration (“UF”) removed data over a treatment performed by the dialysis machine; sending the UF removed data and at least one of the blood pressure data or the patient weight data to a server; determining at least one of a UF trend, a blood pressure trend or a patient weight trend from the UF removed data, the blood pressure data or the patient weight data, respectively; and displaying at least one of the UF trend, the blood pressure trend or the patient weight trend so that a therapy adjustment can be made if necessary.

Abstract: A system and method for monitoring a patient's compliance with a medication regimen includes an electronic tag integral with or attached to a medicine delivery device such as a capsule, the tag having an antenna and a receiver/transmitter, the system also including a reader positioned externally for detecting the presence and location of the delivery device in the patient.

Abstract: A system is provided for integrating conformal electronics devices into apparel. The system includes a flexible substrate onto which a flexible device is disposed. The flexible device can include a stretchable coil that can be used to receive and transmit near field communications. The flexible device also includes an integrated circuit component and a memory unit. In some examples, the device also includes a sensor that is configured to record measurement of the wearer of the apparel and/or the surrounding environment.

Abstract: Various embodiments of a power source and method of forming such power source are disclosed. The power source can include a substrate and a cavity disposed in a first major surface of the substrate. The power source can also include radioactive material disposed within the cavity, where the radioactive material emits radiation particles; and particle converting material disposed within the cavity, where the particle converting material converts one or more radiation particles emitted by the radioactive material into light. The power source further includes a sealing layer disposed such that the particle converting material and the radioactive material are hermetically sealed within the cavity, and a photovoltaic device disposed adjacent the substrate. The photovoltaic device can convert at least a portion of the light emitted by the particle converting material that is incident upon an input surface of the photovoltaic device into electrical energy.

Abstract: A phototherapy device for treating neonatal hyperbilirubinemia comprises a plurality of LEDs coupled to a support structure configured to absorb and dissipate heat generated by the LEDs without requiring a fan. The LEDs provide a uniform dose of radiation on a treatment surface of the subject over a distance range of 20 cm to 45 cm. The support structure can comprise a heat-conductive metal plate. The LEDs have an emission range of 400 nm to 520 and a light output intensity of at least 30 ?W/cm2/nm and at most 65 ?W/cm2/nm at the treatment surface. The device can be adjustably coupled to a mounting structure. Power supplied to the LEDs is adjustable based on the total number of hours of use of he LEDs, the intensity of the LED radiation, the distance between the LEDs and the treatment surface, and/or the tilt or orientation of the phototherapy device.

Abstract: Systems and methods for providing registration at a remote site that may include, for example, a monitoring module that may communicate with a remote site. A registration protocol may be used by the monitoring module and the remote site in generating the messages communicated during the registration process. The monitoring module may gather and generate various identification information to be included in the registration protocol messages. The registration information provided by the monitoring module maybe stored at the remote site in a database server having a database. A confirmation message may be communicated from the remote site to the monitoring module that may either acknowledge successful registration or report that an error occurred during the registration process.

Abstract: An example renal therapy system includes a blood pressure monitor configured to output blood pressure data concerning a patient and a renal therapy machine communicatively coupled to the blood pressure monitor. The renal therapy machine is configured to generate ultrafiltration (“UF”) removed data from a prescribed renal therapy treatment performed by the renal therapy machine on the patient, and transmit the UF removed data and the blood pressure data via a network. At least one of a UF trend or a blood pressure trend from the UF removed data or the blood pressure data is determined, enabling a further determination as to at least one of (a) whether a prescribed renal therapy treatment adjustment or a new prescribed renal therapy treatment needs to be made, (b) whether the patient is complying with the prescribed renal therapy treatment, or (c) whether a condition related to an alarm or an alert exists.

Abstract: A wearable computer is used for monitoring process data in road finishing. The wearable computer receives process data of the road finishing process. In the event of process data lying outside a predetermined range, the wearable computer effects alerting of the wearer of the wearable computer.

Abstract: An example dialysis system includes a dialysis machine and a receiver coded with at least one of an address or a personal identification number (“PIN”). The dialysis machine is configured to perform a prescribed dialysis treatment on a patient, generate ultrafiltration (“UF”) removed data over the prescribed dialysis treatment performed by the dialysis machine, and transmit the UF removed data. The example receiver is configured to receive sensor data from a sensor attached to the patient. The at least one coded address or PIN ensures that the sensor data is received by the receiver as opposed to another receiver.

Abstract: A wearable device may include: a strap including a substantially polygonal opening and a buckle formed at one end thereof; a buckle part configured to fasten opposite ends of the strap to each other by binding the opposite ends of the strap; and a body configured to be coupled to the opening by being fitted into the opening or decoupled from the opening. The body may include a front surface and a rear surface, and a display having a substantially polygonal shape when viewed from the top on the front surface, and a biometric sensor disposed on the rear surface.

Abstract: Methods, systems, and devices for wireless communication are described. In some wireless communications systems, a wireless device may identify a set of at least two wireless communications channels that are available for communication with another wireless device. In some examples, the wireless device may identify at least one channel of the set, and may select integrity check information that indicates the identified wireless channel(s) that are available. The wireless device may then transmit the integrity check information during a first time period. In some examples, a wireless device may receive wireless communication that includes integrity check information on a subset of channels. The wireless device may then determine, based on the integrity check information, whether the identified subset of channels is the same as the actual subset of channels used for transmission of the wireless communications.

Abstract: A body fluid component measuring system which is capable of continuous measurement and reduces downtime includes a sensor unit which is positionable indwelling in the skin of a subject and which measures a predetermined body fluid component included in the body fluid of the subject; and a transmission unit which is detachably attached to the sensor unit and which calculates blood glucose level based on measurement data measured by the sensor unit, and transmits the calculated blood glucose level to a display unit. Identification information for establishing communication between the transmission unit and the display unit is stored in the sensor unit, and the transmission unit, upon activation, uses the identification information read out by the sensor unit to establish communication with the display unit.

Abstract: Systems and methods may provide for identifying sensor data associated with an intraoral device and analyzing a chemical composition of an ingestible product based on the sensor data. Additionally, a notification may be selectively generated based on the chemical composition. In one example, analyzing the chemical composition includes determining the level of one or more of an allergen, a toxin or a predetermined substance in the ingestible product.

Abstract: Sensors are attached to a living being so as to generate corresponding sensor signals. A monitor is in communications with the sensors so as to derive physiological parameters responsive to the sensor signals. Predetermined limits are applied to the physiological parameters. At least one indicator responsive to the physiological parameters and the predetermined limits signal the onset of a sepsis condition in the living being.

Abstract: An optical proximity sensor assembly includes an optical proximity sensor with an IR LED emitting light having an infrared wavelength, an IR photo detector sensitive to the infrared wavelength, an optical barrier blocking direct light rays from the LED to the IR photo detector and permitting reflected light rays to reach the at least one photo detector; and an electronic integrated circuit with an amplifier for amplifying a signal detected by the photo detector, an analog to digital converter, LED drivers, noise reduction and ambient light cancellation circuitry, and a digital interface for communication with a microcontroller. The optical proximity sensor is accommodated on a wearable carrier. A single sensor may include a plurality of identical or different LEDs, a plurality of photodiodes, or both. Also, several sensors may be placed on a person's skin along a vascular path to obtain data relating to blood flow and artery stiffness.

Abstract: Systems and methods for determining the effectiveness of breath training regimens are disclosed. The systems include a sensor assembly configured to detect data indicative of at least one physiological parameter of a user during breath training sessions while the user is awake and while the user is asleep. The system also includes an electronic computing unit with a processor configured to analyze the data indicative of the at least one physiological parameter of the user detected by the sensor assembly, and determine effectiveness of the breath training sessions on the user by determining trends of the at least one physiological parameter of the user from the analyzed data, and determining changes in the at least one physiological parameter of the user while the user is asleep occurring during a period of time from the determined trends.

Abstract: Systems, devices, and methods for controlling access to a medical device are provided. One example system includes an access card configured to wirelessly transmit user identification information and a medical device configured to receive the user identification information from the access card, and enable access to one or more components of the medical device based on permission information associated with the received user identification information. One example medical device includes a plurality of device components; a data receiver configured to wirelessly receive user identification information; a memory configured to store permission information in association with the user identification information; and a processor configured to retrieve the permission information from the memory in response to receiving the user identification information from the data receiver, and enable access to the one or more device components based on the retrieved permission information.

Abstract: Devices, systems, and methods are disclosed for relaying information from a cardiac pacemaker to an external device. Logic on the pacemaker modulates a heartbeat clock of the pacemaker to encode information onto a blood pressure sequence by adding or subtracting a small subinterval to or from a pulse repetition interval of the pacemaker. A muscle stimulator beats the heart according to the modulated sequence. A monitoring device external to the body monitors the blood pressure to retrieve the encoded information, or message. The encoded information is then decoded to determine the information in the message. This information may concern the pacemaker as well as other devices within the body that communicate with the pacemaker such as blood monitors, etc. Since the message is conveyed via simple modulation of the heart beat intervals, no separate transmitter is required in the pacemaker which would otherwise increase cost and decrease battery life.

Abstract: Techniques for charging and communication with electronic devices, such as headphones, are provided. Specifically, systems and methods to provide charging of, and communication with, audio devices, such as by photovoltaic (PV) cells, infrared (IR) illumination, audio signals, and LEDs such as laser LEDs, are disclosed.

Abstract: An inserter assembly for continuous glucose monitoring with medication delivery capability where the assembly has a deployment button containing a needle deployment mechanism having a sharp held in a pre-release position, a housing body in which the deployment button is movably received within a top end of the housing body, the housing body having a sensor deployment assembly containing a lumen and a sensor disposed within the lumen and extending out of the lumen to a circuit board that is part of the sensor deployment assembly, the sensor deployment assembly matingly connected to the sharp where the sharp extends beyond the sensor deployment assembly and contains the sensor not fixedly attached to the sharp, and a sensor housing releasably received within a lower end of the housing body, the sharp extending into a sensor deployment assembly recess within the sensor housing and directly above a sensor opening in a bottom of the sensor housing.

Abstract: An inserter assembly for continuous glucose monitoring with medication delivery capability where the assembly has a deployment button containing a needle deployment mechanism having a sharp held in a pre-release position, a housing body in which the deployment button is movably received within a top end of the housing body, the housing body having a sensor deployment assembly containing a lumen and a sensor disposed within the lumen and extending out of the lumen to a circuit board that is part of the sensor deployment assembly, the sensor deployment assembly matingly connected to the sharp where the sharp extends beyond the sensor deployment assembly and contains the sensor not fixedly attached to the sharp, and a sensor housing releasably received within a lower end of the housing body, the sharp extending into a sensor deployment assembly recess within the sensor housing and directly above a sensor opening in a bottom of the sensor housing.

Abstract: A wireless power supply system of the present invention performs wireless power supply between a power transmission coil installed at a parking space and a power reception coil mounted on a vehicle, transmits judging power for judging a parking position from the power transmission coil to the power reception coil in an operation of parking the vehicle in the parking space, and sets an excitation frequency of the judging power to a frequency lower than an in-phase resonance point or higher than an anti-phase resonance point.

Abstract: A headpiece for use with a cochlear implant including a headpiece housing, a retention magnet within the headpiece housing that generates a retention magnetic field, the retention magnet including a bottom surface that faces the cochlear implant, a top surface opposite the bottom surface, and an outer radial surface between the top and bottom surfaces, an induction coil within the headpiece housing that transmits audio signals to the cochlear implant by generating a telemetry magnetic field, and a retention flux guide within the headpiece housing and adjacent to the top surface of the retention magnet.

Abstract: A passive implantable relay module includes a first coupler arm configured to wirelessly receive electromagnetic energy radiated through electric radiative coupling from a transmitting antenna located outside a subject's body; a second coupler arm; and a connector portion comprising a first metal core and a first dielectric coating surrounding the first metal core, the connector portion configured to connect the first coupler arm to the second coupler arm such that when the passive implantable relay module is implanted inside the subject's body and the transmitting antenna initiates wireless energy transfer to the first coupler arm via non-inductive coupling, electromagnetic waves carrying the electromagnetic energy received at the first coupler arm propagate along the first metal core to arrive at the second coupler arm, where the electromagnetic energy arriving is wirelessly transferred, again via non-inductive coupling, to a receiving antenna on a passive wireless neural stimulator device.

Abstract: A sensor network system that includes a sensor array having a plurality of sensor units that include a plurality of sensor elements, each sensor element configured to generate an electrical signal in response to a chemical environment in the vicinity of the sensor unit. The set of electrical signals generated by the sensor elements of the sensor unit represents a measured signature of the environment in the vicinity of the sensor unit. An analyzer is configured to extract the measured signatures of each sensor unit from sensor unit information signals and to detect a presence and concentration of one or more of the gases of interest based on the measured signatures.

Abstract: Methods, system and devices for monitoring a plurality of parameters associated with a closed loop control operation including continuously monitoring a physiological condition and automatic administration of a medication, detecting an adverse condition associated with the monitored physiological condition or the medication administration deviating from a predetermined safety level of the closed loop control operation, and initiating a non-zero pre-programmed medication delivery rate are provided.

Abstract: A phone comprising: a phone body, at least one sensor on the phone body for measuring a vital sign of a user when the phone is held in use; means for converting the vital sign measurement into a voice-frequency band signal; and means for transmitting the voice-frequency band signal for use in monitoring the health of the user.

Abstract: A wearable remote device includes a user interface, a strap configured to removably secure the wearable remote device to a wrist of a patient such that the user interface is accessible by the patient, and a wireless transceiver configured to wirelessly communicate with a wearable defibrillator. The wearable remote device includes a processor coupled to the user interface and wireless transceiver to provide a notification relating to at least one of device information relating to the wearable defibrillator and a cardiac arrhythmia communicated by the wearable defibrillator via the wireless transceiver. Responsive to a determination that the notification is of an urgent nature, the processor is configured to cause the user interface to communicate the notification, and responsive to a determination that the notification is not of an urgent nature, cause the user interface to store information relating to the notification in a memory of the wearable remote device.

Abstract: A capsule endoscopic system is disclosed for receiving data from a capsule device and providing inductive power to the capsule device wirelessly, where the capsule endoscopic system incorporates a feature to automatically protect the capsule device and the docking device from damage if the capsule device is docked in a backward orientation. In one embodiment, the docking device comprises a current sense circuit to detect the current flowing through the primary coil or primary drive circuit. The occurrence of wrong orientation can be detected from the current. A detection/control circuit can be used to provide the needed control in order to prevent damage to the system. In another embodiment, a resonant circuit comprising a capacitor and the primary coil is used to provide the needed protection when the capsule device is docked with a wrong orientation.

Abstract: Example disposable biosensor devices having an activity sensor are disclosed. One example device includes a disposable biosensor that has a first electrode having a distal end to be inserted into a subcutaneous layer beneath a person's skin, the first electrode having a reactive material disposed on the distal end, and a second electrode. The disposable biosensor device also includes an activity sensor that can be activated upon an activity by the person, the activity sensor for detecting the activity and providing data about the activity. The disposable biosensor also includes a radio frequency transmitter for transmitting data obtained from the first or second electrode and the activity sensor.