A processor of a medical device configured to communicate with a remote server can be programmed to protect the medical device from exposure to unauthorized or malicious software. A system or method to implement this form of protection can include, for example, at least one processor on the medical device, a control software module that controls the operation of the medical device and is executable on the processor, a data management module that manages data flow to and from the control software module from sources external to the medical device, and an agent module that has access to a limited number of designated memory locations in the medical device. In addition, a hemodialysis apparatus can be configured to operate in conjunction with an apparatus for providing purified water from a source such as a municipal water supply or a well. A system for controlling delivery of purified water to the hemodialysis apparatus can comprise a therapy controller of the hemodialysis apparatus configured to communicate with a controller of a water purification device, and a user interface controller of the hemodialysis apparatus configured to communicate with the therapy controller, and to send data to and receive data from a user interface.

A processor of a medical device configured to communicate with a remote server can be programmed to protect the medical device from exposure to unauthorized or malicious software. A system or method to implement this form of protection can include, for example, at least one processor on the medical device, a control software module that controls the operation of the medical device and is executable on the processor, a data management module that manages data flow to and from the control software module from sources external to the medical device, and an agent module that has access to a limited number of designated memory locations in the medical device. In addition, a hemodialysis apparatus can be configured to operate in conjunction with an apparatus for providing purified water from a source such as a municipal water supply or a well. A system for controlling delivery of purified water to the hemodialysis apparatus can comprise a therapy controller of the hemodialysis apparatus configured to communicate with a controller of a water purification device, and a user interface controller of the hemodialysis apparatus configured to communicate with the therapy controller, and to send data to and receive data from a user interface.

Provided is a control device (20, 20a) for controlling an operation of an aerosol nebulizer system (30), said aerosol nebulizer (system 30) comprising an aerosol generator (31) for nebulizing a liquid or an aerosol source for dispensing aerosol, said control device (20), 20a comprising: a communication unit (21, 21a), configured to establish a first wireless communication connection and to perform first data transmission with the aerosol nebulizer system (30), a control unit (22, 22a), configured to evaluate a progression of identifications received via the first data transmission and received in association with aerosol nebulizer data units respectively related to a usage of the aerosol nebulizer system (30).

A computer-implemented method, a medical device, and a system for acquiring user-specific customization data, i.e. user-specific language packages, are provided. The computer-implemented method comprises: determining a first set of user-specific customization data stored on the medical device; comparing the first set of user-specific customization data with a second set of user-specific customization data that is required by a user; and upon determining that the second set of user-specific customization data is different from the first set of user-specific customization data, acquiring, from a data storage external to the medical device, the second set of user-specific customization data or a delta between the first set and the second set of user-specific customization data.

A computer-implemented method, a medical device, and a system for acquiring user-specific customization data, i.e. user-specific language packages, are provided. The computer-implemented method comprises: determining a first set of user-specific customization data stored on the medical device; comparing the first set of user-specific customization data with a second set of user-specific customization data that is required by a user; and upon determining that the second set of user-specific customization data is different from the first set of user-specific customization data, acquiring, from a data storage external to the medical device, the second set of user-specific customization data or a delta between the first set and the second set of user-specific customization data.

A system has a plurality of diagnostic sensors and a first computing device interconnected to the plurality of diagnostic sensors for: commanding the plurality of diagnostic sensors to collect diagnostic data from a patient, determining if each of the plurality of diagnostic sensors are positioned at respectively predefined body locations of the patient, combining the collected diagnostic data for analysis when all of the plurality of diagnostic sensors are positioned at respectively predefined body locations of the patient, and prompting the patient to reposition at least one of the plurality of diagnostic sensors when the at least one sensor is determined as being mis-positioned from the corresponding predefined body location.

The system (100) and method for bio-medical samples (07) identification and resource optimization, as compared to prior-arts, is capable to continuously read and record, without manual-intervene, multiple bio-medical sample holders, individually/in groups and provides effective recording, communication and resource management of bio-medical sample holders and resource management at a processing point. System (100) has an outgoing mail pick-up bin (40) at a collection point (10) that continuously scans multiple RFID tags (32) of the bio-medical sample tagged holders (30) dropped therein at an instant to achieve digital data and by use of the RFID communication device (44) connected to a cloud network (20) intimates a processing point (50) to plan for resources optimization before bio-medical arrival of bio-medical samples and the location of dispatch. The collection point (10) does not have to manually scan and record and hence increases efficiency.

The system (100) and method for bio-medical samples (07) identification and resource optimization, as compared to prior-arts, is capable to continuously read and record, without manual-intervene, multiple bio-medical sample holders, individually/in groups and provides effective recording, communication and resource management of bio-medical sample holders and resource management at a processing point. System (100) has an outgoing mail pick-up bin (40) at a collection point (10) that continuously scans multiple RFID tags (32) of the bio-medical sample tagged holders (30) dropped therein at an instant to achieve digital data and by use of the RFID communication device (44) connected to a cloud network (20) intimates a processing point (50) to plan for resources optimization before bio-medical arrival of bio-medical samples and the location of dispatch. The collection point (10) does not have to manually scan and record and hence increases efficiency.

Devices, systems, and techniques for controlling delivery of therapy for diabetes are described. In one example, a system includes a wearable device configured to generate user activity data associated with an arm of a user; and one or more processors configured to: identify at least one gesture indicative of utilization of an injection device for preparation of an insulin injection based on the user activity data; based on the at least one identified gesture, generate information indicative of at least one of an amount or type of insulin dosage in the insulin injection by the injection device; compare the generated information to a criteria of a proper insulin injection; and output information indicative of whether the criteria is satisfied based on the comparison.

The present specification describes methods and systems for modifying a media, such as Virtual Reality, Augmented Reality, or Mixed Reality (VR/AR/MxR) media based on a vision profile and a target application. In embodiments of the specification, a Sensory Data Exchange (SDE) is created that enables identification of various vision profiles for users and user groups. The SDE may be utilized to modify one or more media in accordance with each type of user and/or user group.