A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.

An aerosol delivery device may include a rechargeable power source configured to provide power to generate an aerosol, device electronics configured to generate the aerosol responsive to application of the power from the power source, and an authentication module. The authentication module may include a separate chip or circuit board relative to the device electronics. The authentication module may be inserted into the aerosol delivery device between the power source and the device electronics to control provision of the power to the device electronics for generation of the aerosol or between the power source and a charge port of the aerosol delivery device to control charging of the power source.

Systems for the treatment and prevention of pelvic dysfunction are provided. In one embodiment, a vaginal dilation device includes a handle portion and a shaft portion. The shaft portion is configured to expand from a collapsed configuration to an expanded configuration. The shaft portion can include a distal tip region, a spine region, and a distal arm region connecting the distal tip region to the spine region. The spine region can extend distally from the handle portion to the distal arm region, and can be generally tubular in shape. The distal arm region can be generally conical in shape and be configured to provide a gradual increase in diameter from the distal tip region to the spine region. Methods of use are also provided.

The invention relates to a delivery device for nasal medication. It addresses need for delivering medication to the nose of a patient. In a preferred embodiment the device has: •A transducer 10 adapted to create an ultrasonic focal zone; •a feeder chamber 13 holding medication; •an energising chamber 14 smaller than the feeder chamber; •a mesh 15; and •an exit 17. The device is formed so that when it is activated the feeder chamber 13 continuously fills the energising chamber 14 with medication (until the feeder chamber has insufficient medication left to achieve this) so that there is a substantially constant supply of medication within the focal zone able to be energised and forced from the energising chamber so as to contact the mesh, become an aerosol, and leave the device by way of the exit.

The invention provides an insufflation apparatus having a housing and a gas generator arranged to be, at least partially, mounted to the housing. The housing includes a gas outlet for delivering gas to a patient and a gas storage chamber arranged to store gas and deliver it to the gas outlet. The gas generator includes a cartridge mount on the housing adapted to receive a gas generating cartridge, the gas generating cartridge containing gas generating material that generates gas that is delivered to the gas storage chamber. The invention also provides alternative insufflation apparatus, a gas cartridge and a method of generating insufflation gas.

Example embodiments relate to a method of protecting a surface of an e-vaping device portion from corrosion, the method including preparing a coating mixture configured to protect the surface from corrosion, and coating the surface with a protective coating based on the coating mixture, wherein the coating is performed via one of electrodeposition, dipping, spraying, and vapor deposition, and the coating mixture includes at least one of a silane and a resin.

Superior dilatation devices and methods of using such devices are contemplated which are effective for providing enhanced levels of sexual stimulation as well as enhancing the treatment or amelioration of conditions which may be treated with dilatation, such as vaginismus and other forms of dyspareunia, pelvic floor dysfunction, and certain other forms of incontinence. By positioning a tubular balloon around the shaft of a conventional rigid dilatation device, providing a reservoir inside the body of the device containing an inflation fluid like helium gas, and using a pump to transfer the inflation between the two, the balloon may be inflated and deflated repeatedly and on command. Through particular control systems, potentially including biofeedback elements and arrangements of multiple balloon lumens, the inflation/deflation sequence may be customized and optimized to produce an enhanced stimulative or treatment effect.

Described herein is a respiratory therapy system comprising: a primary power supply, a secondary power supply, and a breathing apparatus configured to provide respiratory therapy. The breathing apparatus comprises a controller. There is a connection between the primary power supply and the breathing apparatus configured to facilitate transmission of power and data between the primary power supply and the breathing apparatus. The controller is configured to monitor a parameter of the primary power supply, and disengage the primary power supply if the parameter differs from a parameter threshold. The controller is configured to engage the secondary power supply on disconnection of the primary power supply such that the breathing apparatus can continue operation without interruption.

A device for filling a reservoir. The device includes a cover portion comprising a septum window, and a bottom portion, the bottom portion configured to attach to a disposable housing assembly comprising the reservoir, wherein the cover portion and the bottom portion are rotatably attached in a locked configuration and wherein in a locked configuration, a septum is obscured through the septum window, wherein when the cover portion and the bottom portion are placed in an unlocked configuration, the cover portion rotates with respect to the bottom portion and the septum is visible through the septum window.

A device (102) provides respiratory treatment for SDB (including mild OSA) and other respiratory conditions. A flow generator warms and humidifies gas at controlled flow levels. For example, the device (102) delivers breathable gas to the upper airway at flow rates of about 10-35 Liters/minute. Levels of flow rate, temperature and/or humidification of the device may be automatically adjusted in response to the detection of SDB events. The device may also automatically deliver adjustments of any of the levels in accordance with detected phases of respiratory cycles. In sane embodiments, the device automatically delivers distinct levels to either of the nares based on independent control of flow to each nare. A warm-up procedure controls temperature and humidity at a desired target during a ramp-up of flow to the set therapy level. A cool-down procedure controls temperature above the dewpoint to avoid condensation internal to the device and patient interface.