Abstract: One or more systems for automated preparation of a regenerative epidermal suspension comprises a base unit, a cartridge assembly containing a cup, and a tissue disaggregator. The system may also include related tools. The system executes one or more sequences wherein a first motor actuates the pestle against a tissue sample that is disposed along a screen within the cup while the tissue sample is in contact with, in sequence, an enzyme solution, a first buffer solution, and then a second buffer solution. To transition between fluidic contact stages or steps, the tissue disaggregator engages with and lifts the cup into a raised position within a processing area of the cartridge while a base plate motor rotates the appropriate well into alignment under the cup for each processing step. Once the sequence is complete, a user may draw up a regenerative epidermal suspension through an opening in the cartridge top cover.

Abstract: One or more methods for automated preparation of a regenerative epidermal suspension comprises a processor receiving an initiation signal that indicates that a cartridge that has a cover, a cup containing a tissue sample, and a well plate situated beneath the cover that has a first well containing an enzyme solution and a second well containing a buffer solution, has been placed on a sensor, executing a sequence that actuates a tissue disaggregator against the tissue sample in the cup positioned in the first well, raises the cup to an upper position, rotates the well plate to position the second well beneath the cup, lowers the cup to a position within the second well, and actuates the tissue disaggregator against the tissue sample in the second well.

Abstract: One or more methods for treating a tissue site comprises collecting a tissue sample that has keratinoytes and placing the tissue sample in a cartridge that has a well plate, positioning the cartridge within a base unit that has a tissue disaggregator, activating the base unit to rotate the well plate to align wells in the well plate with the tissue sample and the tissue disaggregator, operate the tissue disaggregator to separate the tissue sample to form a regenerative epidermal suspension, and provide the regenerative epidermal suspension to a tissue site to enhance healing of the tissue site.

Abstract: One or more methods for automated preparation of a regenerative epidermal suspension comprises a processor receiving an initiation signal that indicates that a cartridge that has a cover, a cup containing a tissue sample, and a well plate situated beneath the cover that has a first well containing an enzyme solution and a second well containing a buffer solution, has been placed on a sensor, executing a sequence that actuates a tissue disaggregator against the tissue sample in the cup positioned in the first well, raises the cup to an upper position, rotates the well plate to position the second well beneath the cup, lowers the cup to a position within the second well, and actuates the tissue disaggregator against the tissue sample in the second well.

Abstract: One or more methods for treating a tissue site comprises collecting a tissue sample that has keratinoytes and placing the tissue sample in a cartridge that has a well plate, positioning the cartridge within a base unit that has a tissue disaggregator, activating the base unit to rotate the well plate to align wells in the well plate with the tissue sample and the tissue disaggregator, operate the tissue disaggregator to separate the tissue sample to form a regenerative epidermal suspension, and provide the regenerative epidermal suspension to a tissue site to enhance healing of the tissue site.

Abstract: One or more cartridges for preparation of a regenerative epidermal suspension comprises a cover with a raised processing opening, a cup that can be received within the raised processing opening and has a screen, and a well plate that is positioned under the cover, has a well, and rotates relative to the cover such that the well aligns with the raised processing opening. One or more cartridges for preparation of a regenerative epidermal suspension comprises a cover with an opening that can receive a tissue sample.

Abstract: One or more systems for automated preparation of a regenerative epidermal suspension comprises a base unit, a cartridge assembly containing a cup, and a tissue disaggregator. The system may also include related tools. The system executes one or more sequences wherein a first motor actuates the pestle against a tissue sample that is disposed along a screen within the cup while the tissue sample is in contact with, in sequence, an enzyme solution, a first buffer solution, and then a second buffer solution. To transition between fluidic contact stages or steps, the tissue disaggregator engages with and lifts the cup into a raised position within a processing area of the cartridge while a base plate motor rotates the appropriate well into alignment under the cup for each processing step. Once the sequence is complete, a user may draw up a regenerative epidermal suspension through an opening in the cartridge top cover.

Abstract: Disclosed herein are devices, methods, systems and kits adapted for vitrification and/or reanimation of oocytes, embryos or blastocysts. The device includes a straw and a filter, wherein the straw comprises a lumen traversing through the straw and has a proximal section, a middle section and a distal section and wherein the filter is affixed in the straw and comprises a plurality of pores having a diameter smaller than the diameter of said oocytes, embryos or blastocysts but large enough to allow the passage of a fluid composition therethrough.

Abstract: A method and apparatus for performing mitral valve chordal repair on a patient include attaching at least one filament to a mitral valve leaflet and to a papillary muscle. A first end of a filament can be attached to the mitral valve leaflet and the length of the filament can be adjusted by adjusting the tension of the filament in a catheter. The second end of the filament can be attached to an attachment site.

Abstract: A method and apparatus for performing mitral valve chordal repair on a patient include attaching at least one filament to a mitral valve leaflet and to a papillary muscle. A first end of a filament can be attached to the mitral valve leaflet and the length of the filament can be adjusted by adjusting the tension of the filament in a catheter. The second end of the filament can be attached to an attachment site.

Abstract: A catheter system for use in minimally invasive cardiac surgical procedures. The catheter system diminishes certain trauma generally associated with invasive cardiac procedures while providing aortic occlusion, extracorporeal circulation, cardiac arrest, and cardiac venting. The catheter system provides a minimally invasive and simplified system that performs total cardiopulmonary bypass with ease of insertion, shortened recovery periods, and improved whole body perfusion wherein the upper body is perfused independently of the lower body. The catheters are refined, with reduced diameters and specialized functions for maximum control of each aspect of cardiopulmonary bypass.

Abstract: A method of surgery including bending a multi-purpose surgical implement handle that has proximal and distal ends. A gripping section is located toward the proximal end, and an attachment section is located toward the distal end. An adjusting section is interposed between the gripping section and the attachment section. The adjusting section may be bent by a human user at virtually any discrete location along the section. The adjusting section may include an increased-adjustability portion which is easier to bend than other portions of the adjusting section. The method includes attaching a surgical implement to the attaching section of the handle, and bending the adjusting section at least once prior to inserting the implement through a surgical opening to a surgical field. The method further may include bending the adjusting section more than once to form multiple bends therein.

Abstract: A surgical knife which provides improved multi-sided incisions and is preferably allows for a substantially cruciate, or cross-shaped incision. The surgical knife includes a handle and a multi-bladed portion located at one end of the handle. The handle is sized and configured to maximize grip and surgical manipulation thereof. The multi-bladed portion is formed from a primary blade and a secondary blade. The primary blade is configured with two exemplary primary blade members. The primary blade members are formed with sharpened edges which combined to form a sharpened distal point of the primary blade. The secondary blade is formed with sharpened edges and cooperates with the primary blade. The coupling of the primary blade and the secondary blade is such that the distal end of the secondary blade is located at a distance from the sharpened distal point of the primary blade.

Abstract: A surgical knife which provides improved multi-sided incisions and is preferably allows for a substantially cruciate, or cross-shaped incision. The surgical knife includes a handle and a multi-bladed portion located at one end of the handle. The handle is sized and configured to maximize grip and surgical manipulation thereof. The multi-bladed portion is formed from a primary blade and a secondary blade. The primary blade is configured with two exemplary primary blade members. The primary blade members are formed with sharpened edges which combined to form a sharpened distal point of the primary blade. The secondary blade is formed with sharpened edges and cooperates with the primary blade. The coupling of the primary blade and the secondary blade is such that the distal end of the secondary blade is located at a distance from the sharpened distal point of the primary blade.

Abstract: A catheter system for use in minimally invasive cardiac surgical procedures. The catheter system diminishes certain trauma generally associated with invasive cardiac procedures while providing aortic occlusion, extracorporeal circulation, cardiac arrest, and cardiac venting. The catheter system provides a minimally invasive and simplified system that performs total cardiopulmonary bypass with ease of insertion, improved whole body profusion, and shortened recovery periods. The catheters are refined, with reduced diameters and specialized functions for maximum control of each aspect of cardiopulmonary bypass.

Abstract: A multi-purpose surgical implement handle has proximal and distal ends. A gripping section is located toward the proximal end, and an attachment section is located toward the distal end. An adjusting section is interposed between the gripping section and the attachment section. The adjusting section may be bent by a human user at virtually any discrete location along the section. The adjusting section may include an increased-adjustability portion which is easier to bend than other portions of the adjusting section.

Abstract: An aortic knife which provides multi-sided incisions within an aorta for effectuating improved aortotomies. The aortic knife includes a handle and multiple blades radiating from the handle. The handle is sized and configured to maximize grip and surgical manipulation thereof. The multiple blades radiate outwardly and proximally from a distal sharpened point. A substantially cruciate, or cross-shaped, incision results from four sharpened blades extending from the distal sharpened point. Alternatively, the multi-bladed configuration of the aortic knife may comprise three, five, or six or more blades. The blades form equal angles in radiation outwardly and proximally from the distal sharpened point. The method of the invention requires obtaining an appropriately sized aortic knife which is stabbed into a portion of an aorta. An anvil of an aortic punch is then inserted into the incision in the aorta without the stretching necessitated by the conventional single linear incision.

Abstract: The present invention is directed to new and useful methods and apparatus for isolating and immobilizing tissue for improved presentation in a surgical site, preferably in coronary bypass on a beating heart. At the same time, the present invention also helps avert ischemic damage to tissues downstream. A surgical stabilizer in accordance with the present invention offers physical manipulation of a surgical site, which improves the surgeon's sewing, grasping, and visualizing abilities at the site, and in turn, may increase the confidence and patency of the graft. The stabilizer is used to compress or to suction a region of the heart just below a stenotic coronary artery. The surgeon may selectively articulate the tissue by spreading it apart or pushing it together, as per his or her preference, or per the requirements of the surgical situation. The surgeon may lock in place the handle via a ratchet mechanism to hold the specific open or closed articulation of the surgical stabilizer.

Abstract: The present invention is directed to new and useful methods and apparatus for improving access to the heart during cardiac surgery, while avoiding damage to the phrenic nerves. The present invention comprises a heart elevation apparatus which is soft and substantially cylindrical, with substantially flat anterior and posterior surfaces. Upon inflation, the anterior surface stabilizes the positioning of the heart and prevents the heart from falling off of the apparatus. The flat posterior surface facilitates positioning of the apparatus on the chest wall. An insulation pad on the posterior surface serves to insulate the phrenic nerves from the frigid bathes commonly employed in cardiac surgical procedures, and also protects the nerves from any compressive forces exerted during the surgery.

Abstract: An endoscope has a fiber optic image bundle which is insertible into a separate sterile sleeve such that the fiber optic image bundle need not be sterilized prior to use. A window formed proximate the distal end of the sleeve facilitates viewing through the fiber optic image bundle. A contractile member urges the fiber optic image bundle into abutment with the window to facilitate proper optical alignment of the distal end of the fiber optic image bundle with the window.