A device to administer multiple capsules or pills or a combination of capsules or pills into the mouth of an animal. The device is gravity fed and is composed of seven parts. The parts are: (i) a molded tee handle, (ii) a molded trigger pin (tee handle), (iii) a spring pin (trigger release pin) which is part of the molded trigger; (iv) a torsion spring; (v) a tube which can be 6 inches long with an outer diameter such as ½ inch with varying inner diameters resulting from different interior thicknesses of the barrel; (vi) a ⅜ inch ID #4 pan head screw; and (vii) a ⅞ inch diameter disc.

Systems, devices, and methods for delivering an implant to the orbit. In some instances, the systems may include a delivery device having a tongue member and a handle. The delivery device may further include an ejector configured to deliver an implant from the tongue member. The delivery device may also include a piercing member configured to create an opening in tissue. The systems may further include a piercing member for creating an opening in tissue. In some instances, the piercing member may have a first blade member rotatably connected to a second blade member.

A composition for use in the treatment of fistula, the composition comprising activated carbon.

The invention pertains to an applicator (1) for inserting an implant, in particular a rod-like implant (2) containing an active substance, under the skin of a human or animal, comprising a housing (3), a cannula (6), a cannula holder (9), an implant (2) accommodated inside the cannula (6) and/or the cannula holder (9), a protective cover (7) for the cannula (6), and a mechanism (22, 23, 7) which, at least after the cover (7) has been removed from the cannula (6), secures the implant (2) inside the cannula (6) and/or cannula holder (9). The mechanism (22, 23, 7) disengages the implant (2) during insertion of the cannula (6) or after the cannula (6) has been inserted. Substantially no lateral force will be exerted during the expelling of the implant from the cannula.

A drug dosage form is provided in the form of a solid tablet which is greater than 50% by weight the local anesthetic agent. The local anesthetic agent may be selected from the group consisting of an aminoamide, an aminoester, and a combination thereof. The drug tablet may be in the form of a mini-tablet which is greater than 70 wt % drug, with the balance being excipient. For example, the anesethetic agent may include lidocaine, in a salt or base form, combined with binder and lubricant excipients. Implantable drug delivery devices including the tablets are also provided, e.g., one or more of the drug tablets may be contained in a biocompatible housing. The drug tablets may be substantially cylindrical with flat end faces, and the device may have from 10 to 100 drug tablets aligned in the housing with the flat end faces of adjacent tablets abutting one another.

An applicator for insertion and lubrication of a body lumen is disclosed having an elongate, hollow, cylindrical outer sheath including a receiving cup at a distal end for receiving a lubrication capsule; and a plunger slidingly received within the elongate, hollow cylindrical outer sheath, the plunger including a piercing element at a distal end adapted to extend into the receiving cup. A liquid-filled soft gel capsule is placed in the receiving cup, and the piercing element is used to puncture the capsule located in the receiving cup prior to insertion of the applicator into the body lumen, and wherein the plunger can be depressed once the applicator is inserted into the body lumen to eject the pierced capsule into the body lumen.

The dispensing device includes a hollow tube having an open upper end and an open lower end, as well as a horizontal bar disposed between the walls of the hollow tube adjacent to the open lower end. A disc is movably positioned within the hollow tube, the disc having a central aperture defined therein. A string or other flexible member has one end secured to the disc. The other end of the string is drawn downward in the tube, looped around the horizontal bar, then drawn upward through the central aperture in the disc and out the open upper end of the tube. A semi-solid medication is loaded in the tube between the disc and the open lower end of the tube. When the string is pulled out of the upper end of the tube, the disc is drawn downward, dispensing the medication.

A minimally traumatic trocar system is described. The trocar system includes a cannula, a plastic obturator, and hydrodissection microcannula. The cannula includes a tubular cannula body and blunt anterior surface. The obturator includes an anterior rounded tip. The hydrodissection microcannula includes an anterior rounded tip and an opening proximate to the anterior rounded tip. The cannula and plastic obturator assemble to form a minimally traumatic trocar by passing the plastic obturator through an interior passage of a tubular cannula body of the cannula. The hydrodissection microcannula probes an incision to form an insertion path while causing minimal trauma. The assembled trocar probes the incision along the insertion path to reach a delivery site within subcutaneous tissue. The plastic obturator withdraws from the cannula and at least one medication pellet is loaded within the interior passage. The plastic obturator pushes the medication pellet(s) through the interior passage to the delivery site and deposits the medication pellet(s) within the subcutaneous tissue.

The invention pertains to apparatuses, means and methods to promote uptake of biocompatible fluids into a reservoir of an implantable drug delivery system though a porous membrane. Embodiments of the invention promote fluid uptake by creating a pressure differential between the reservoir of the drug delivery device and the biocompatible fluid outside the device.

A solid medication insertion device includes a barrel having an insertion end portion and a proximal end portion opposite the insertion end portion and having a continuous side wall extending therebetween that defines an interior area. A medicament is initially positioned in the interior area of the barrel. The medication insertion device includes a plunger slidably coupled to the barrel that has a first end engaging a proximal end of the medicament, the plunger having a cylindrical configuration selectively slidable from a starter configuration extending away from the proximal end portion of the barrel to a deployed configuration positioned downstream inside the interior area of the barrel. Pressure applied to the plunger causes the plunger to urge the medicament downstream within the interior area of the barrel. The medication insertion device, i.e., the suppository applicator, is constructed using a material consisting essentially of hemp plastic.