There is provided herein a system and a method for an insertion device positioning guidance system comprising: an electromagnetic field generator configured to generate an electromagnetic field covering a treatment area; a plate sensor configured to be positioned within the treatment area in a location defining an orientation of a subject; a reference sensor configured to be positioned, within the treatment area, on the subject's torso, the reference sensor is configured to define a reference coordinate system representing the position and orientation of the subject's torso relative to said field generator; a registration sensor configured to mark at least a first and a second anatomic locations relative to the reference coordinate system; and a processor configured to operate said field generator, read signals obtained from said the plate sensor, said reference sensor and said registration sensor, calculate a position and orientation thereof relative to said field generator, generate a 3D anatomic map representing the torso of the subject and the first and second anatomic locations, said processor is further configured to facilitate visualization on the 3D anatomic map of a position, orientation and/or path of a tip sensor, located in a distal tip section of the insertion device, with respect to the first and second anatomic locations, independent of the subject's movement and independent of deviations in the position and/or orientation of said field generator, thus determination of a successful medical procedure is facilitated.

A flow control apparatus adapted for a feeding set includes a housing capable of receiving at least a portion of the feeding set and a pumping device for acting on the feeding set to produce fluid flow in the feeding set for delivery of fluid. The apparatus has a sensor arranged with respect to the pumping device to produce a signal indicative of a rotational position of a rotor, and a control circuit in communication with the sensor for receiving the sensor signal from the sensor indicative of the rotational position of the rotor and in communication with the pumping device to control operation thereof. The control circuit controls operation of a motor at a first output to rotate the rotor to produce fluid flow in the feeding set and at a second output effectively less than the first output.

Gastric and intestinal feeding tube devices and methods can be enhanced to provide better patient outcomes. For example, this document provides gastric and intestinal feeding tube devices that include an external bumper with pressure sensors and pressure indicators that facilitate usage of the feeding tube devices within an appropriate range of skin surface pressure. This document also provides external bumpers with deflectable elements that facilitate the application of a controlled amount of force between the external bumpers and the skin surface.

A flow control apparatus comprising a housing capable of receiving a portion of the feeding set, a pumping device configured to receive the feeding set and may produce a fluid flow in the feeding set and deliver fluid to a subject, an ultrasonic sensor may be configured to produce a sensor signal indicative of a condition of the feeding set, and a control circuit in communication with the ultrasonic sensor for receiving the sensor signal from the ultrasonic sensor indicative of the condition of the feeding set. The ultrasonic sensor may comprise a plurality of sensor components which may be configured to emit an ultrasonic signal in a first direction, and in a second direction opposite the first direction through the feeding set.

A feeding system for medical patients comprises a storage assembly, dispensing assembly, and extension set including, in part, a reservoir, a pump, a feeding tube, a check valve and an adapter. The reservoir is configured to hold at least one feeding of nutritional substance. The dispensing assembly is connected to the storage assembly and pumps the at least one feeding of nutritional substance from the reservoir to the feeding tube connected to an outlet of the pump. The check valve unit is connected to a second end of the feeding tube by means of a check valve connection point and is configured to allow the flow of nutritional substance in only one direction. The at least one feeding of nutritional substance is passed through the adapter unit connected to the check valve unit.

A pump set for use with a pumping apparatus to deliver nutrition to an infant includes a first container to receive breast milk; a second container to receive fortifier; tubing extending from the first container and from the second container; and a valve mechanism connected to the first and second containers by the tubing and configured to selectively pass liquid from the first container and the second container.

A gastrostomy device (100) comprises a gastrostomy tube (200) having a retainer lumen (235) extending between a proximal part and a distal part of the tube (200); and an inflatable retaining element (300) coupled to the tube (200) at the distal part. An interior space of the retaining element (300) is in fluid communication with the retainer lumen (300). The gastrostomy device (100) also comprises an indicator (410) being in fluid communication with the retainer lumen (235) at the proximal part of the tube (200). The indicator (410) is configured for indicating a pressure in the retaining element (300) continuously within a range from a pressure corresponding to an empty retaining element (300) to an optimal pressure for the inflated retaining element (300).

The present specification is directed to systems, devices, and methods of portable enteral pump systems for feeding and/or flushing an ambulatory patient. Embodiments provide an enteral pumping device that may be loaded by a patient from a front and a top side of the pumping device and is therefore more convenient to use. Further, embodiments incorporate a single rotor pump for dual-use purposes of feeding nutrients and flushing fluids to the patient. A pinch valve is placed between the parallel sides of the two tubes to cut off fluid flow when required. At least one sensor is also placed between the rotor pump and an outlet. The sensors are used to detect occlusions and the type of disposables used, among other purposes.

Systems, devices, and methods are disclosed for maintaining oral hydration. A device may include a perforated tube, covered by an outer cover made of an absorbent material. The tube may be shaped such that it allows a patient using the device to open and close his or her jaw, without displacement and also to allow other medical devices to be used on the patient simultaneously.

A tester includes: an inlet, connectable to an aspirator tube; an outlet connectable to a vacuum source; and a chamber between the inlet and the outlet, the chamber including: a first tester arranged such that fluids drawn into the chamber by the vacuum source come into contact therewith; a second tester arranged such that fluids drawn into the chamber by the vacuum source pass through it; and a reservoir between the first tester and the second tester; where the first tester includes a first substance adapted to change color in the presence of a target substance, and where the second tester includes colorimetric capnometer, which exhibits a color change in the presence of carbon dioxide, the in-line tester further including a liquid-stop device which, when dry, permits passage of gas from inlet to outlet, but when wetted by liquid, inhibits or prevents the passage of fluids from inlet to outlet.