An absorbent stoma pad for encapsulating an external bolster of a feeding tube is provided. The stoma pad includes an upper layer, base layer, absorbent material, and cavity. The upper layer, which includes an upper surface and a lower surface, contains a centrally located opening with respect to a periphery of the upper layer, wherein the opening is configured to receive a tube portion of the feeding tube. The base layer, which includes an upper surface and a lower surface, contains a centrally located opening with respect to a periphery of the base layer, wherein the opening is also configured to receive the tube portion of the feeding tube. Meanwhile, the absorbent material is disposed adjacent the upper layer's lower surface. Further, the cavity permits airflow between the absorbent layer and the base layer when the external bolster is encapsulated by the stoma pad and positioned within the cavity.

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.

A device to assist with the insertion of a nasal bridle includes an insertion guide and an introducer that is attached to bridle tape. The guide is switchable between two configurations: a substantially straight configuration and a second configuration in which an exit aperture at an upper end of the guide is either at a downwardly oriented angle and/or displaced laterally from the guide longitudinal axis, for example by causing the upper end of the guide to adopt a u-bend. The guide is inserted into a nostril while straight and then adopts its second configuration. The introducer is pushed through the guide and, at the exit, is guided beyond the septum into and out of the opposite nostril. Introducer and tape are pulled through the nasal passage before removing the guide. The guide therefore ensures that introducer and tape are held clear of the septum, reducing discomfort.

Tube holding assemblies and methods for using and making the same are provided.

A bite device is configured to be placed in the mouth (92) of a patient, facilitates insertion of soft tubes (91) from the outside into the mouth (92) of the patient, and includes a bite member (2) and an auxiliary member (3). The bite member (2) includes an abutment portion (21), a biting portion (216) extending outwardly from one side of the abutment portion (21), a sleeve portion (22) opposite to the biting portion (216), and a central hole (23) for insertion of one soft tube (91) therethrough. The auxiliary member (3) includes a fixing plate structure (31) having a main auxiliary hole (317) removably sleeved on the sleeve portion (22), and at least one secondary auxiliary hole (318) for insertion of another soft tube (91) into the mouth (92) of the patient.

A nasogastric tube securing device is an apparatus designed to hold various medical tubes that enter through a person's nose without the use of adhesive tape. A first configuration of the device will attach to an upper lip area of a patient allowing the tube to enter upward into the nasal cavity. A second configuration will attach to the distal end of a nose with a downward facing clip that also holds the tube as it enters the nasal cavity. In both configurations, the clip system used utilizes a plastic sliding track that holds the tube and allows it to slide back and forth, either across the upper lip or side to side along the user patient's nose. The tube clip on the track permits one tube to be exchanged for another one without removing the adhesive, thus eliminating repeating trauma to the skin area. Both clip systems are held in place with Allevyn? Adhesive, Mepilex? silicone foam dressing, or similar product to further reduce skin irritation.

A multi-diameter clipping mechanism includes an adhesive member, a connecting member, a first and a second clipping members, and an engaging member. The connecting member is connected to the adhesive member. The first clipping member has a guiding trough and a resilient arm. The second clipping member and the engaging member are assembled to the first clipping member. The second clipping member has an engaging tongue and unidirectionally inclined teeth. The engaging member has an engaging salient and a press portion at two ends thereof. When the second clipping member enters the guiding trough, one of the teeth engages with the engaging salient. When the press portion is pressed against the resilient arm by an external force, the engaging member pivots against the first clipping member to disengage the engaging salient from the tooth, thereby making the second clipping member leave the guiding trough.

Gastrostomy tubes and systems and methods for implanting them are provided. In one example, the gastrostomy tube includes an elongate tubular member including a first end sized for introduction into the patient's mouth, a second end including an expandable member or other bumper, and a feeding lumen extending between the first and second ends. A bolster is connectable around the first end after the first end has been directed from within the patient's stomach through intervening tissue and extends from the patient's skin and the bumper is placed against the wall of the stomach. An adapter is connectable to the bolster after the first end and excess material of the tubular member beyond the bolster has been separated, the adapter including a connector for removably connecting to a feeding tube.

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.