The present invention relates to a fitting for an enteral feeding line, comprising: attachment means configured to connect the fitting to a complementary fitting, a tapered tip coaxial with an axis and a flange extending around the tip and coaxial with the tip, the flange extending away from the tip and delimiting with the tip an annular space configured to receive the complementary fitting, the attachment means being disposed at the annular space, the annular space comprising a first portion comprising the attachment means and a second portion not provided with attachment means, the second portion having an axial length along the axis and the tip having a predetermined diameter at an interface I between the first portion and the second portion, a ratio of the predetermined diameter to the axial length being greater than or equal to 1.0 and less than or equal to 2.0.

A nasogastric tube connector device includes an annular connector body for detachably engaging a through hole of a respirator mask having an inner peripheral surface defining a space, and a fixed member having a first concave surface and two side surfaces cooperating with the inner peripheral surface to define an opening of the space for passing of a nasogastric tube therethrough. A first plug member is detachably inserted through the opening into the space, and includes a second concave surface cooperating with the first concave surface to define a main tube hole communicating with the space. A second plug member is detachably inserted into the main tube hole to sealingly close the opening.

An endotracheal tube apparatus according to an example of this disclosure includes a brace for attachment to a patient's face, a support extending from the brace and including a groove for receiving an endotracheal tube. A clamp surrounds the support and the endotracheal tube. The clamp is comprised of a polymeric material

The invention relates to systems for securing a tube (e.g. feeding tube) and/or a patient interface or a dermal patch to a user. One embodiment comprises a holder, an interface side of the holder attachable to the patient interface or the dermal patch for securing a feeding tube to the patient interface or the patch, the holder comprising at least a first channel or recess for receiving the feeding tube to couple the feeding tube to the patient interface. Another embodiment comprises a patient interface itself comprising a backing for positioning on a patient's face, a dermal patch having a patient side and an interface side, the patient side of the patch attachable to the user, the patch comprising at least a first flap portion attachable to the tube for affixing the tube to the patch, a two-part releasable connection arrangement for releasably securing the patient interface to the patch.

The invention relates to systems for securing a tube (e.g. feeding tube) and/or a patient interface or a dermal patch to a user. One embodiment comprises a holder, an interface side of the holder attachable to the patient interface or the dermal patch for securing a feeding tube to the patient interface or the patch, the holder comprising at least a first channel or recess for receiving the feeding tube to couple the feeding tube to the patient interface. Another embodiment comprises a patient interface itself comprising a backing for positioning on a patient's face, a dermal patch having a patient side and an interface side, the patient side of the patch attachable to the user, the patch comprising at least a first flap portion attachable to the tube for affixing the tube to the patch, a two-part releasable connection arrangement for releasably securing the patient interface to the patch.

A gastrointestinal catheter for insertion into a treatment site in a patient, the treatment site including at least one of a first treatment site and a second treatment site, where the catheter includes at least one of a first and a second treatment member; the proximal portions of the first and second treatment members may be detachably or slidably conjoinable side by side; the distal portions of the first and second treatment members are separate from each other. The distal end of the first treatment member is configured for insertion into the first treatment site; the second treatment member is configured to be placed at a second treatment site. The distal end region of the first treatment member has an anchoring configuration adapted to anchor the distal end region within the first treatment site, the distal end region is further capable of elastically assuming a linear constrained configuration.

A balloon catheter system includes a tube and a dilator detachable from the tube after the tube is inserted into a cavity in the patient. The cavity may be filled with gas or liquid to expand the viscera surrounding the cavity and the guidewire may be inserted using a trochar, for example. The tube includes one or more lumen to expandable balloons that are inflatable by fluid inserted through the lumen and into the balloon or balloons, which are formed by elastic film sealed on opposite ends to the external diameter of the tube. The dilator is held in place during insertion, such as by a stainless steel shaft and a sheath portion of the dilator extending over the end of the tube being inserted into the cavity. A portion of the sheath may extend over and protect the balloon. A retractor net may be used to capture and remove the dilator or the dilator may be designed as a bioabsorbable or digestible material or of a material that passes safely through the digestive tract of a patient.

The invention relates to a PEG probe having a PEG tube, an outer holding plate, through which the PEG tube is fed and in which the PEG tube is fastened, and a funnel adapter, which is associated with an outer end region of the PEG tube. A tightly closing valve is arranged either in the PEG tube between the outer holding plate and the outer end region or on the outer end region of the PEG tube. The valve blocks the flow through the PEG tube in a closed position and allows said flow at least in the full cross-section of the PEG tube in an open position. The valve has a valve body and a valve housing. The valve body is connected to and movable by means of a handle accessible from outside. The valve body is supported in the valve housing.

A securing pocket for managing the loose portion of a medical tube, such as a Nasogastric/Nasojejunal tube, while an implanted portion of the medical tube remains attached to the patient. The loose portion of the medical tube has a coiled section disposed within a receptacle formed between flexible front and rear panels. An integral flap overlaps the front panel to selectively close the receptacle and may be secured with a snap connector. Jam cleats are located along left and right edges adjacent a top edge of the receptacle. Each jam cleat forms a breach in the receptacle through which a tethered section of the loose medical tube extends. The jam cleats are configured to apply a progressive wedge force on the tethered section of the loose medical tube in response to tension along the tube. The jam cleat has flexible sides formed in a V-shape.

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.