A medical device for use during radiation therapy may include a longitudinal body configured to be positioned within a urethra. The longitudinal body may include a lumen, a distal end, and a proximal end. A first balloon may be coupled to a distal portion of the longitudinal body and fluidly connected to a first port at the proximal end of the longitudinal body. A second balloon may be positioned between the first balloon and the proximal end of the longitudinal body and fluidly connected to a second port at the proximal end of the longitudinal body.

The invention relates to a wetting mechanism 20 for wetting a tube 12 of a catheter 10. The wetting mechanism 20 includes a housing 16 positioned initially at or proximal to the tip end 13 of the catheter tube 12. The housing 16 comprises a wetting chamber 23 into which at least a portion of the catheter tube 12 is able to be introduced and be moved therethrough to wet the catheter tube 12 in use. The wetting mechanism 20 includes a wetting applicator 40 positioned within the wetting chamber 23 configured to hold fluid therein and release said fluid to wet the catheter tube 12 upon movement of the tube 12 through the wetting chamber 23.

A urinary catheter support configured to support an indwelling urinary catheter such that the urinary catheter is secured relative to the penis of a male patient includes a flexible main body having an interior size and configured to receive and accommodate the penis of the male patient. A catheter support is located at a front end of the main body and is configured to support a catheter adjacent a longitudinal axis of the main body. A slot extends along the longitudinal axis through the main body and the catheter support. A strap includes first and second end segments and a middle segment between the first and second end segments. The first and second end segments respectively extend through first and second openings in the main body, and the middle segment extends through an interior of the main body.

An antimicrobial, antiseptic, and antibacterial barrier has a flexible shield configured to slidingly engage a urinary catheter. The shield has one or more sections configured to conform and adhere to the urinary meatus and/or surrounding skin or tissues of a target patient. A flexible expandable drape is engaged with the shield and is axially aligned with the catheter to provide an additional layer of protection to prevent the passage of bacteria, fungi, and contaminants into the urinary tract. The shield and drape each comprise an antimicrobial, antiseptic, and antibacterial material.

A system and method for nonsurgical penile girth enhancement. Hydro-dissection creates a space along a length of the penis between Buck's Fascia and Darte's fascia. The filler material, such as hyaluronic acid, is injected into the space created and is modeled after injection. During the same procedure or a later procedure, additional spaces can be created and injected with the filler material, until the desired girth is obtained. The amount of filler material injected during any given procedure is limited to avoid challenging the lymphatics of the penis. By staging the girth enhancing injections, the risk of penile granulomas can be minimized, if not eliminated.

The present invention relates to a device that secures a straight or Foley catheter in the urinary tract of a male subject. The device includes a portion that can be coupled to the subject's penis and a portion that can be coupled to the straight or Foley catheter. The present invention also relates to methods of making and using this device and to assemblies including the device and a straight or Foley catheter.

A urinary catheter conveying device includes a sleeve member, a conveying assembly and a controller. The sleeve member is for sleeving onto a glans of a penis and has a guiding hole to be registered with an external urethral orifice of the glans. The conveying assembly includes a casing removably mounted to the sleeve member, and a conveying mechanism for advancing the urinary catheter to the guiding hole such that the urinary catheter is inserted into the external urethral orifice. The controller controls the conveying mechanism to advance the urinary catheter to the guiding hole. A urinary catheterization system and a method of using the urinary catheterization system are also disclosed.

A penis erection stimulation system comprises one or more infusion needles disposed within and implanted along with one or more housings adjacent the patient's left and right corpora cavernosa. A reservoir and a pump are also implanted inside the patient's body to supply the infusion needle with infusion liquid. A drive unit also adapted for implantation inside the patient's body is arranged for advancing and retracting the tip end of the infusion needle such that it penetrates the housing at least in two different penetration areas either simultaneously or in immediate time succession, thereby injecting drugs along with the infusion liquid into the patient's body for stimulating penis erection.

The present disclosure provides compositions and methods for using topical, isotonic compositions comprising a prebiotic oligosaccharide, a metal co-factor, and an essential oil comprising bornyl acetate. The compositions support the genital microbiota and are useful for, for example, hydrating, lubricating, cleaning, and/or decreasing irritation or inflammation of the urogenital and/or anogenital region of a subject, and/or enhancing the beneficial genital microbiota of a subject. Such compositions are useful before, during, and/or after sexual and/or reproductive activity. Kits for gel compositions including these compositions are also provided which may be used to aid delivery to and administration in low-resource settings.

An at least partly implantable system for injecting a substance into a patient's body, in particular a penis erection stimulation system, comprises one or more long, flexibly bendable infusion needles, the tip ends of which are disposed within and implanted along with at least one first housing, in particular adjacent the patient's left and right corpora cavernosa. The respective other end or ends of the infusion needles are disposed and implanted along with at least one second housing remote from the first housing. A reservoir and a pump are also implanted inside the patient's body to supply the infusion needle with infusion liquid. A drive unit also adapted for implantation inside the patient's body is arranged for advancing and retracting the infusion needle such that its tip end penetrates the at least one first housing's outer wall in at least one penetration area, more specifically at least in two different penetration areas either simultaneously or in immediate time succession, thereby injecting the substance into the patient's body.