Abstract: A pump module is provided for use in a medical fluid dispensing system that includes a pump body made of a non-compliant material and first and second pump chambers formed in the body. Each of the chambers has a first, open end and an opposite, closed end. The pump module further includes first and second pistons in the first and second pump chambers, respectively. At least one fluid inlet and a fluid outlet are selectively in fluid communication with the first and second pump chambers. Each of the pistons extends through the open end of a respective one of the pump chambers, with each of the pistons being operably translatable within the pump chamber toward and away from the closed end of the chamber. The pistons are translatable independently of one another.

Abstract: A device for administering a fluid product including a housing, a conveying device for the product, a coupling element provided for the drive of the conveying device and which can be rotated about a rotational axis, a first blocking element connected in a rotationally secure manner to the coupling element, a second blocking element detachably engageable with the first blocking element thereby preventing a rotational movement thereof in the drive direction and enabling said rotational movement to take place in the counter dosing direction, a torsion spring connected to the coupling element such that it is stressed by the rotational movement when the blocking elements are engaged in a blocked position and drives the coupling element in a rotary manner after the blocking position is released, and a release element coupled to at least one of the blocking elements such that a release movement of the release element displaces at least one of the blocking elements from the blocked position, the release element also

Abstract: A system for the metering and delivery of small discrete volumes of liquid is comprised of a small or minimal number of inexpensive components. One such component is a movable member, such as a miniature precision reciprocating displacement pump head, which is driven by an actuator that comprises a shape memory alloy material. The operating mechanism of the system is of little or minimal complexity. The system facilitates the precise metering and delivery of the small discrete volumes of liquid. Potential applications for the system include subcutaneous, long-term, automated drug delivery, for example, the delivery of insulin to a person with diabetes. In such an application, the small, simple and inexpensive nature of the invention would allow for its use as both a portable and a disposable system.

Abstract: The present invention provides a safety needle/catheter system and method of use for dialysis procedures. The invention includes a safety feature that prevents inadvertent needle sticks by administrators. The invention further includes a catheter portion composed of shape memory materials. The catheter portion has a deformed shape and size that facilitates insertion of the catheter portion and closure of the catheter incision and a recovered shape and size that can reduce the severity of infection and/or clotting, as well as provide improved maintenance and control over proper fluid volume flow during dialysis.

Abstract: A catheter shaft and methods for making and using the same. The catheter shaft may include a core portion, a cap portion, and one or more lumens. The cap portion may be disposed on or over a section of the core portion and define a region with a different exterior or interior surface characteristic. For example, the cap portion may define a lubricious region along the catheter shaft. Manufacturing the catheter shaft may include a modified co-extrusion process that incorporates a flow valve on at least one of the material supply lines so that the supply line can be regulated by a user.

Abstract: An access device includes a body, a first tube, a second tube, and a mechanism. The first and second tubes extend through the body. The mechanism operably couples the first and second tubes such that at least one tube is pivotable about an axis with respect to the other tube. The body may form a substantially fluid-tight seal at the incision. In another embodiment, the access device further includes a third tube extending through the body and the mechanism operably couples the tubes together such that at least two tubes are pivotable about the axis with respect to the remaining tube.

Abstract: A seal assembly for use with an access device includes a seal housing defining a central longitudinal axis, an inner wall and an outer wall. The inner wall defines a longitudinal opening to permit passage of instrumentation through the seal housing. A gimbal mount is at least partially accommodated within a space defined between the inner wall and the outer wall of the seal housing. The gimbal mount includes a seal member defining an aperture for substantial sealed reception of a surgical instrument. The gimbal mount is adapted for angular movement relative to the central longitudinal axis upon angulation of the surgical instrument while substantially maintaining the sealed reception of the surgical instrument.

Abstract: A system and/or apparatus for delivering a medical device into a body includes an elongate tubular member and a valve fitted within a proximal end thereof. The valve preferably includes a tubular body and a flap, wherein the tubular body is engaged within the proximal end of the tubular member and has an open end approximately aligned with a proximal termination of the proximal end of the tubular member. The flap of the valve preferably extends over a hole formed in an end wall of the tubular body opposite a side of the end wall that faces a passage of the tubular body, which passage extends between the open end and the end wall. The hole communicates with the passage and with the lumen of the tubular member, and the flap is movable away from the hole when the device is introduced through the passage and the hole.

Abstract: A syringe has a syringe barrel into which a plunger stopper is inserted during a manufacturing process. A plunger rod is connected to the plunger stopper, and a backstop for preventing inadvertent removal of the plunger stopper from the syringe barrel is arranged at the proximal end of the syringe barrel. The backstop and the plunger rod are configured to form a combined assembly component which is adapted to be mounted to the syringe barrel in a combined manufacturing step. After mounting the combined assembly component to the syringe barrel, the backstop and the plunger rod are separated to allow conventional use of the syringe.

Abstract: A valve apparatus for medical applications, comprises a flexible member extending across a lumen through which a flow of materials is to be controlled. The flexible member includes a plurality of movable elements formed on opposite sides of a slit extending through the flexible member. The moveable members are biased so that when a pressure less than a predetermined threshold value is applied to the flexible member, the moveable elements are maintained in a closed position in which no flow is permitted past the flexible member and, when a pressure at least as great as the threshold value is applied to the flexible member, the moveable elements are moved to an open position separated from one another along the slit permitting flow through the lumen.

Abstract: A device, system and method for occluding fluid flow through an infusion set detached from a patient's body. The device includes a means for detecting loss of contact to a patient's body and activating an occlusion mechanism accordingly.

Abstract: A wax heating device for wax treatment of human skin that includes a contained a controlled exothermic chemical reaction to melt wax on a flexible element for contacting human skin. A heating pouch contains a first portion. A heater element has an inner area with a first portion holding a heat generating material and a second portion holding an actuation agent, with a seal that is broken to actuate the heat generation and melt the wax.

Abstract: A wound contact device comprising a permeable material and a wound contact layer having voids extending through the contact layer to a depth in the permeable material. The wound contact layer can comprise a thin sheet or film forming a generally flat and smooth wound contact surface having essentially no discontinuities or gaps. The wound contact layer can comprise a thin sheet of highly calendered fabric forming a wound contact surface having a mean surface roughness in the range of about 0 microns to about 200 microns. In progressive wound healing, an embodiment of the wound contact device having the fabric contact surface is used in earlier healing stages and an embodiment of the wound contact device with film contact surface is used in later healing stages. The wound contact device is particularly useful in wound dressings for use in suction-assisted wound therapy.

Abstract: The present invention relates to a set of coupling parts, such as parts for coupling an ostomy bag to a base plate, said base plate being adhered around a stoma. The set of coupling parts provides a connection part that may be interposed between a first coupling part and a second coupling part and where the coupling parts may be connected and disconnected from each other by the same movement of the connection part.

Abstract: An absorbent article is disclosed in which an absorbent body intervenes between a liquid permeable front sheet and a back sheet. A middle-height portion is provided by thickening a front surface of an approximately center area of the absorbent body with respect to a standard portion absorbent body. The article includes leakage preventing grooves which extend to a longitudinal direction of the absorbent article are provided on both sides which sandwich a body fluid discharge portion area in the area of the middle-height portion, respectively.

Abstract: An absorbent article for fecal matter handling, especially with respect to mushy and/or pasty fecal matter, along with methods of making the same. A composite bodyside liner can reduce the amount of fecal matter that remains on the skin of a wearer after removal of the absorbent article from the wearer. The bodyside liner can include only a fluid pervious liner layer. Alternatively, the bodyside liner can include a fluid pervious liner layer and a surge layer. A fecal adhering treatment composition is applied to at least a portion of the bodyside liner to reduce the amount of fecal matter that remains on the skin of the wearer after the absorbent article is removed.

Abstract: A protective undergarment system for absorbing fluids released by the body of a user. The protective undergarment system includes an upper member being designed for being selectively positioned around an abdomen, a groin and a posterior of the user. The upper member comprises a lower aperture extending through the upper member whereby the lower aperture is designed for extending from a portion of the groin to a portion of the posterior and passes between the legs of the user. A lower member is selectively coupled to the upper member whereby the lower member is selectively positioned over the lower aperture of the upper member to selectively close the lower aperture of the upper member. The lower member is designed for absorbing the fluids released by the body whereby the lower member can be removed from the lower member when the lower member is soiled.

Abstract: During diastolic coronary perfusion, blood perfuses through the heart via the coronary arteries. Delivery of a therapeutic and/or diagnostic agent to the heart during diastolic coronary perfusion allows the therapeutic and/or diagnostic agent to efficiently perfuse through the heart. A medical device according to the invention detects closure of the aortic valve of a heart, and initiates delivery of a therapeutic and/or diagnostic agent upon detection of aortic valve closure. The medical device detects aortic valve closure by processing a signal.

Abstract: The invention provides biodegradable implants for treating sinusitis. The biodegradable implants have a size, shape, density, viscosity, and/or mucoadhesiveness that prevents them from being substantially cleared by the mucociliary lining of the sinuses during the intended treatment period. The biodegradable implants include a sustained release therapeutic, e.g., an antibiotic, a steroidal anti-inflammatory agent, or both. The biodegradable implants may take various forms, such as rods, pellets, beads, strips, or microparticles, and may be delivered into a sinus in various pharmaceutically acceptable carriers.

Abstract: The invention provides biodegradable implants for treating sinusitis. The biodegradable implants have a size, shape, density, viscosity, and/or mucoadhesiveness that prevents them from being substantially cleared by the mucociliary lining of the sinuses during the intended treatment period. The biodegradable implants include a sustained release therapeutic, e.g., an antibiotic, a steroidal anti-inflammatory agent, or both. The biodegradable implants may take various forms, such as rods, pellets, beads, strips, or microparticles, and may be delivered into a sinus in various pharmaceutically acceptable carriers.

Abstract: The invention provides biodegradable implants for treating sinusitis. The biodegradable implants have a size, shape, density, viscosity, and/or mucoadhesiveness that prevents them from being substantially cleared by the mucociliary lining of the sinuses during the intended treatment period. The biodegradable implants include a sustained release therapeutic, e.g., an antibiotic, a steroidal anti-inflammatory agent, or both. The biodegradable implants may take various forms, such as rods, pellets, beads, strips, or microparticles, and may be delivered into a sinus in various pharmaceutically acceptable carriers.

Abstract: The invention provides biodegradable implants for treating sinusitis. The biodegradable implants have a size, shape, density, viscosity, and/or mucoadhesiveness that prevents them from being substantially cleared by the mucociliary lining of the sinuses during the intended treatment period. The biodegradable implants include a sustained release therapeutic, e.g., an antibiotic, a steroidal anti-inflammatory agent, or both. The biodegradable implants may take various forms, such as rods, pellets, beads, strips, or microparticles, and may be delivered into a sinus in various pharmaceutically acceptable carriers.

Abstract: The invention provides biodegradable implants for treating sinusitis. The biodegradable implants have a size, shape, density, viscosity, and/or mucoadhesiveness that prevents them from being substantially cleared by the mucociliary lining of the sinuses during the intended treatment period. The biodegradable implants include a sustained release therapeutic, e.g., an antibiotic, a steroidal anti-inflammatory agent, or both. The biodegradable implants may take various forms, such as rods, pellets, beads, strips, or microparticles, and may be delivered into a sinus in various pharmaceutically acceptable carriers.

Abstract: The invention provides biodegradable implants for treating sinusitis. The biodegradable implants have a size, shape, density, viscosity, and/or mucoadhesiveness that prevents them from being substantially cleared by the mucociliary lining of the sinuses during the intended treatment period. The biodegradable implants include a sustained release therapeutic, e.g., an antibiotic, a steroidal anti-inflammatory agent, or both. The biodegradable implants may take various forms, such as rods, pellets, beads, strips, or microparticles, and may be delivered into a sinus in various pharmaceutically acceptable carriers.

Abstract: A tip wrench/coupler having a generally hollow body for the storage and/or attachment of a tip, and a plurality of fluidic couplers that allow the wrench/coupler to connect two or more handpiece together in series, fluidically, thereby allowing the handpieces to be primed at the same time.

Abstract: A method and system is provided for responding, from internally within a patient, to an atrial arrhythmia in a heart including measuring from within the patient at least one electrocardiogram characteristic indicative of the atrial arrhythmia, and controlling from within the patient drug therapy delivery to the patient responsive to measuring the at least one electrocardiogram characteristic. Drug therapy is initiated to the patient responsive to measuring the at least one electrocardiogram characteristic. According to one aspect of the present invention, the drug therapy is staged within the patient prior to measuring the at least one electrocardiogram characteristic. According to another example embodiment, the heart is paced from within the patient at a predefined rate responsive to measuring the at least one electrocardiogram characteristic, pacing occurring alone, or in combination with drug therapy.

Abstract: A mechanical element allows the tip of the handpiece of a dermatological treatment system to rotate to adjust for deviations in handpiece angle with respect to the surface of the treatment area. The tip may glide over the surface of the skin, the tip may include wheels or rotating cylinders on which the tip rolls across the skin, or the tip may be removed from the skin and placed in a new location in a stamping motion. The tip of the handpiece rotates around a single axis, or around two perpendicular axes, so that pressure on the tip moves the flat surface of the tip into proper orientation for planar contact with the skin. An element can be included in the handpiece to apply a restoring force on the tip so that the tip rests in its optimal position in the absence of external forces.

Abstract: A laser surgical apparatus for performing treatment by irradiating a part to be treated by a laser beam is disclosed. This apparatus includes a laser source which emits the treatment laser beam; a multi-articulated arm for delivering the treatment laser beam emitted from the laser source, the arm including a plurality of light delivery pipes, a joint part for jointing the light delivery pipes, the joint part being rotatable with respect to at least one of the pipes jointed by the joint part, a reflection mirror disposed in the joint part; and a surgical instrument is connected to an end of the arm and used for irradiating the treatment laser beam delivered therein through the arm to the treatment part.

Abstract: A catheter includes a cryoablation tip with an electrically-driven ablation assembly for heating tissue. The cryoablation tip may be implemented with a cooling chamber through which a controllably injected coolant circulates to lower the tip temperature, and having an RF electrode at its distal end. The RF electrode may be operated to warm cryogenically-cooled tissue, or the coolant may be controlled to conductively cool the tissue in coordination with an RF treatment regimen, allowing greater versatility of operation and enhancing the lesion size, speed or placement of multi-lesion treatment or single lesion re-treatment cycles.

Abstract: The present invention provides systems and methods for selectively applying electrical energy to a target location within a patient's body, particularly including tissue in the spine. The present invention applies high frequency (RF) electrical energy to one or more electrode terminals in the presence of electrically conductive fluid or saline-rich tissue to contract collagen fibers within the tissue structures. In one aspect of the invention, a system and method is provided for contracting a portion of the nucleus pulposus of a vertebral disc by applying a high frequency voltage between an active electrode and a return electrode within the portion of the nucleus pulposus, where contraction of the portion of nucleus pulposus inhibits migration of the portion nucleus pulposus through the fissure.

Abstract: An electrosurgical instrument for ablating cartilage while limiting collateral damage includes a non-conducting head with a small electrically conductive surface. The head of the instrument is coupled to a shaft by a flexible portion. The flexible portion biases the electrically conductive surface towards a tissue surface. The head is pivotably coupled to the shaft such that the electrically conductive surface is oriented substantially parallel to the tissue surface as the head slides across the tissue surface. A method of performing electrosurgery includes positioning the electrically conductive surface adjacent to the tissue surface, and sliding the shaft across the tissue surface with the head pivoting such that the electrically conductive surface is oriented substantially parallel to the tissue surface.

Abstract: The invention relates to an ablation catheter which controls the temperature and reduces the coagulation of biological fluids on an electrode of a catheter, prevents the impedance rise of tissue in contact with the electrode, and maximizes the potential energy transfer to the tissue, thereby allowing an increase in the lesion size produced by the ablation. The electrode includes passages positioned to allow blood and other biological fluids to flow into and out of an inner cavity of the electrode. This fluid flow produced the desired cooling effect and is accomplished, for example, by a reciprocating plunger or piston, or by a balloon that is alternately inflated and deflated.

Abstract: According to the present disclosure, a system for sensing attributes of tissue in at least one direction is provided. The system includes a thermal conductivity probe having a sensor configured to measure thermal conductivity in the target tissue in at least one direction, and an electrical conductivity probe having a sensor configured to measure electrical conductivity in the target tissue in at least one direction, a power supply operatively coupled to the thermal conductivity probe and being configured to supply power to the thermal conductivity probe, an impedance analyzer operatively coupled to the electrical conductivity probe, and a computer operatively coupled to at least one of the power supply, the multimeter and the impedance analyzer.

Abstract: A surgical system including a surgical glove having support systems such as, but not limited to, lights, electrical cautery, suction, and irrigation. The surgical glove may include one or more lights, electrical cautery, suction, and irrigation positioned on distal ends of fingers of the surgical glove. The support systems may be controlled with switches positioned on the fingers upon which each support system is positioned. The switches may be operable with the thumb on the human hand upon which the surgical glove is attached. The surgical system may also include a surgical gown having a connection system for attaching support conduit to the surgical gown. The surgical system enables a surgeon to have a plurality of support systems immediately available and reduces entanglement problems endemic with conventional systems.

Abstract: An electrosurgical instrument for spinal procedures comprises an elongated tubular member configured to fit within and be extended down a standard sized cannula. The instrument comprises a proximal end including a handle for the surgeon and supplied with fittings for connection to a source of irrigation fluid and a source of suction. The distal end of the instrument has an active end comprising a slightly-flexible curved wire electrode that extends in the plane of the tubular member. Beyond the wire electrode is an exit port for irrigation fluid, and in front of the electrode is a receiving port for suction. The wire electrode is thus flanked in front by the exiting irrigation fluid and behind by the suction, with the result that fluid flow is drawn by the suction across the wire electrode creating pressure forces that direct removed tissue to the suction entrance and its removal from the surgical site.

Abstract: A novel surgical clamp having a pair of jaws, which may be used to ablate or create leisons in tissue. In embodiment, the jaws have an articulated position wherein the jaws are separated and not parallel to one another, an opened position wherein the jaws are separated and substantially parallel to one another, and a closed position wherein the jaws are adjacent and substantially parallel to one another. One or more of the jaws can articulate independent of the other jaw. Other embodiments are described in the attached specification.

Abstract: An electrosurgical device for use in surgical procedures is disclosed. The electrosurgical device comprises a main body having a proximal end and a distal end. A heat delivery modality is situated and arranged at the distal end of the main body. A sensor arrangement is also situated and arranged at the distal end of the main body. The heat delivery modality provides thermal energy to a tissue being treated while the sensor arrangement is configured to engage and detect a change in dimension of the tissue being treated. Accordingly, the electrosurgical device of the present disclosure allows a surgeon to precisely achieve the desired amount of dimensional change of the tissue being treated.

Abstract: An electrosurgical instrument for treating tissue includes a housing having at least one tissue treating member attached thereto. The tissue treating member includes an electrically conductive tissue contacting surface connected to a source of electrosurgical energy such that the tissue contacting surface is capable of conducting electrosurgical energy to tissue. An energy conductive, ablative material is disposed on the electrically conductive tissue contacting surface and is configured to at least partially deplete during electrosurgical activation to reduce tissue adhesion.

Abstract: An electrosurgical instrument includes a housing having a shaft attached thereto which defines a longitudinal axis therethrough. The instrument also includes first and second opposing jaw members coupled to the shaft, the first jaw member having a conductive surface and movable relative to the second jaw member. The second jaw member is fixed relative to the shaft and includes an electrode rotatable along the longitudinal axis. The rotatable electrode has a sealing surface and a cutting edge. One or more non-conductive stop members are disposed on the first and/or second jaw members that are dimensioned to control the distance between the electrically conductive surfaces when tissue is held therebetween. The jaw members are connected to an electrosurgical energy source such that the jaw members are capable of conducting energy through tissue held therebetween.

Abstract: An orthopedic implant structure is provided for joining and retaining components of a multi-part orthopedic device. The orthopedic implant joining and retaining structure may be embodied in two or more components of the multi-part orthopedic device. In one form, the multi-part orthopedic implant structure is a resilient snap structure such as a resilient flange in one part and a channel structure formed in another part of an orthopedic implant. A channel of the channel structure may have a cavity formed at a rear of the channel that accepts a configured lip formed on an end of the resilient flange. According to another embodiment, the retaining structure includes resilient snap flanges formed on an interconnection component of the multi-part orthopedic implant. A corresponding bore in another part of the multi-part orthopedic implant receives the interconnection component.

Abstract: Apparatus and methods for distracting or compressing distance between a first and second boney structure and for engaging a connecting element.

Abstract: Disclosed are methods and devices for implanting an orthopedic device between skeletal segments, such as vertebrae, using limited surgical dissection. The implanted devices are used to adjust and maintain the spatial relationships of adjacent bones. The implanted device can be, for example, an artificial disc, a fusion cage or any other appropriate device for implantation between skeletal segments.

Abstract: Instruments for inserting an implant in a space between adjacent bony portions include a pair of parallel guide members extending distally from a proximal frame portion. Tamps and impaction instruments facilitate advancement of the implant between the guide members to the space between the adjacent bony portions.

Abstract: A method is provided for treatment of cataract in combination with a glaucoma procedure while maintaining the intraocular pressure by permitting aqueous to flow out of an anterior chamber of the eye through a surgically stented pathway. A trabecular stent is adapted for implantation within the trabecular meshwork of an eye such that intraocular liquid flows controllably from the anterior chamber of the eye to Schlemm's canal, bypassing the trabecular meshwork. Depending upon the specific treatment contemplated, pharmaceuticals may be utilized in conjunction with the trabecular stent enabling post-cataract healing processes.

Abstract: A device, a system employing the device, and method of performing skin treatment are provided for skin treatment. The device includes a vacuum head base defining a chamber therein and having a substantially smooth treatment tip attached and extending from an end thereof or integral therewith. The tip has at least one central opening that is open to the chamber, and is adapted to contact the skin and traverse the skin in a substantially nonabrasive manner. A vacuum access opening is provided through a side wall of the vacuum head base and adapted to connect with a source of vacuum. A tissue stop member is located within the chamber. It may have an abrasive surface for exfoliating skin cells, or a smooth surface for traversing the skin without substantial abrasion.

Abstract: A combination tissue apposition and suture capturing device (100) for performing endoscopic procedures typically in the gastro-esophageal tract. The device (100) is particularly adapted for forming multiple plications used in a gastroplasty procedure devised to cure or ameliorate gastro-esophageal reflux disease. The device include a tissue sewing capsule (102) attached to the distal end of an endoscope having a needle (120) that is deposited in a capsule (102) distal tip cavity following the suturing of a tissue fold and retrieved to enable the suturing of a subsequent tissue fold without the need for multiple intubations. A suture clip delivery device (200) is also disclosed that is adapted to fit within the capsule to enable suture capture without the need for multiple intubations. The combination device eliminates the need for an overtube and maximizes the speed efficiency of the gastroplasty procedure. A method for using the combination device is also disclosed.

Abstract: Devices, systems and methods for retracting, lifting, compressing, supporting or repositioning tissues, organs, anatomical structures, grafts or other structures within the body of human or animal subjects for the purpose of treating a diseases or disorders and/or for cosmetic or reconstructive purposes and/or for research and development purposes or other purposes.

Abstract: A method for creating a plication within a hollow organ. The method uses an elongated member having an end effector attached to its distal end. The end effector has a substantially hollow housing, a fixed jaw extending distally from the housing, and a retractable jaw located within the housing. The method involves the step of inserting the end effector within an organ of a patient such that it is in contact with tissue. The method also involves applying vacuum through the elongated member so as to dispose tissue on the fixed jaw and at least partially within the housing. The method also involves creating a plication by sliding the retractable jaw so that it juxtaposes the fixed jaw.

Abstract: Surgical fasteners are disclosed for terminating flow of fluid through a body lumen, including an outer barrel having an annular side wall having at least a pair of radial slots formed therein, and an inner barrel rotatably and concentrically coupled within the outer barrel. The inner barrel has an annular side wall including a radial slot formed therein corresponding to each radial slot formed in the outer barrel. The surgical fastener has an open position in which the radial slots of the inner of the outer barrel are radially aligned with the corresponding radial slots of the inner barrel and a closed position in which the radial slots of the outer barrel are out of radial alignment with the corresponding radial slots of the inner barrel and constrict the body lumen at two locations along the length thereof. An applier is provided for applying the surgical fasteners.

Abstract: An atherectomy system having a variably exposed cutter wherein a distally located positionable tip closely associated with the cutter and a high pressure fluid jet emanator can be variably and angularly deployed about a hinge mechanism subsequent to entry into the vasculature. The fixed cutter slices or parts atheromatous material and/or thrombotic material from a blood vessel for interaction with high pressure jets to macerate, break up or otherwise reduce the materials for evacuation from the site.