An oscillating apparatus, such as a tattooing apparatus applying an electric motor such as a linear motor, and a first sensor and a controller. A method for controlling an oscillating apparatus such as a tattooing apparatus, includes a controller and various sensors to control, among other things, the position, velocity and acceleration of a needle either directly or via a needle connector.

The invention relates to an extracorporeal blood treatment device comprising a hydraulic system II comprising a plurality of flow paths, the blood treatment device having a control unit 40 which provides an operating mode for disinfecting the hydraulic system with a liquid which can be supplied via one of the flow paths. Moreover, the invention relates to a method for operating an extracorporeal blood treatment device with a hydraulic system comprising a plurality of flow paths. The blood treatment device according to the invention is characterized in that the hydraulic system II has a valve device 23 which provides several switching positions. The valve device 23 has an inlet 25A for the liquid for disinfecting the hydraulic system and a plurality of outlets 26A, 27A, 28A, wherein in a switching position the inlet 25A is connected to one of the outlets 26A, 27A, 28A and in another switching position the inlet is connected to a plurality of outlets 26A, 27A, 28A. The inlet 25A of the valve device 23 is in fluid communication with the flow path via which liquid for disinfecting the hydraulic system II can be supplied, and the outlets 26A, 27A, 28A of the valve device 23 are in fluid communication with another flow path of the hydraulic system, so that liquid can simultaneously be supplied to the individual flow paths.

This invention relates to an ingestible drug delivery device configured for wireless communication with other ingestible drug delivery devices.

Systems and methods are provided for performing a medical procedure within a patient's body that involves a thoracic duct including an ostium communicating with the patient's venous system. A distal end of a catheter is introduced through the patient's venous system into a body lumen adjacent the ostium of the thoracic duct. An expandable member on the distal end of the tubular member may be expanded adjacent the ostium, e.g., within the body lumen or the thoracic duct itself, and used to isolate the thoracic duct from the body lumen, whereupon a medical procedure may be performed via the thoracic duct. For example, lymphatic fluid may be removed from the thoracic duct through a lumen of the tubular member and/or one or more agents may be introduced into the thoracic duct through the tubular member.

A system includes a flow sensor contained within a flow sensor housing, a base, and a seal. The base houses a controller that generates at least one operation modification signal, and the flow sensor is separable from and mountable onto the base. A bottom surface of the flow sensor housing includes the seal. The seal forms a liquid-tight engagement between the flow sensor housing and the base when the flow sensor is mounted onto the base.

A roller clamp assembly for adjusting the fluid flow rate in a connector tube of an infusion set is provided. The roller clamp assembly includes a housing to receive the connector tube, a plate slideably engaged with the housing and configured to rapidly compress the connector tube to provide a coarse fluid flow adjustment, and a roller wheel moveable engaged with the housing and configured to provide a gradual fluid flow adjustment. The plate may be a slide plate received by grooves in an exterior wall of the housing and that moves orthogonally to the connector tube, or the plate may be a shim plate that moves along an interior wall of the housing in parallel to the connector tube. Infusion sets and methods of adjusting fluid flow rates are also provided.

Disclosed herein a real time multipurpose infusion monitoring and controlling unit comprising power source, monitor, micro controller and drop rate sensors, wherein said unit is performing employing horizontal screw mechanism adapted to monitor and control the drip by locking the airdrop in the saline tube to make the drip mechanism more accurately and efficiently.

Methods and apparatuses for detecting tension on a tendon and/or mechanical deformation (e.g., breakage) of one or more steering tendon of a steerable and flexible articulating device. Theses apparatuses may have one or more tendons that are each electrically conductive and configured to steer the apparatus when tension is applied to the proximal end of the tendon. Tension and/or breakage (or other deformation) of one or more of these tendons may be detected by monitoring the electrical resistance of the tendons.

Disclosed are methods, systems, and devices for providing a personalized humidification level. A control system receives, from a first sensor, one or more environmental parameters regarding conditions of the environment. The control system receives, from a second sensor, one or more physiological parameters associated with a user within the environment. The control system determines an action associated with a desired change in the humidity within the environment based, at least in part, on the one or more environmental parameters and the one or more physiological parameters. The control system causes, at least in part, a performance of the action associated with the change in the humidity in the environment based, at least in part, on moisture outputted by a humidifier module. The methods and devices perform the same functionality as the control system.

A pharmaceutical product including a housing that defines a cavity, wherein the cavity stores a pharmaceutical material, and wherein the housing comprises a material configured to dissolve based on contact with a fluid, an ingestible device to encode information in a current signature, wherein the ingestible device is positioned within the housing, and a protective material that encompasses the ingestible device. The ingestible device may be attached to a flexible component, wherein the flexible component is configured to releasably secure the ingestible device within the housing.