Abstract: A biopsy device is provided. The device requires a first elongate substantially tubular member that defines a distal end portion and a proximal end portion with a lumen defined therethrough and a second elongate substantially tubular member that is telescopically and slidably disposed within the lumen of the first member. The second member includes a distal end portion and a proximal portion with a lumen defined therethrough, the distal end portion comprising two or more metallic jaws that are biased toward each other. A third elongate tubular member is telescopically and slidably received within the lumen of the second member, the third member includes a distal end portion with an open distal end, configured to allow foreign material to enter the lumen therefrom, the distal end portion of the third portion configured to maintain the jaws in a separated configured when the jaws surround the distal end portion of the third tubular member.

Abstract: A stent is made from a coiled wire and is very smooth along its length and as well its ends. The stent is thus highly atraumatic to patients, and because of its smooth surfaces, it presents a surface to which it is difficult for microbes to cling. The stent may be used in a minimally invasive procedure, such as for a ureteral stent, and may also be used percutaneously. Similar stents may be used in other body areas, such as in draining the biliary tract, the gastro-intestinal tract, hepatic procedures, and in vascular procedures as well.

Abstract: A sling for supporting a urethra in a patient has characteristics for resisting pull-out, roll-over and a combination of both pull-out and roll-over. To facilitate resistance to pull-out, sling material has protuberances or serrations to resist movement once placed in the patient by the surgeon. Improved resistance to roll-over or roll-up is achieved by providing relief on the sling in areas potentially subjected to roll-over forces by endopelvic fascia. The sling may be used on female or male patients, and may be used in conjunction with a wider support portion to support a bladder and a urethra, rather than a urethra alone. The sling may also be used to support other tissues within a patient.

Abstract: An apparatus and method used in a urological procedure. The apparatus includes a sheath capable of insertion into a passageway within a patient. A filter is provided that includes a mesh that retains any particulate matter that is entrained with the liquid and allows the liquid to pass therethrough. The filter may be removeably attached to receive flow from an outlet of the sheath.

Abstract: A retrieval device for use in renal, biliary, vascular or other systems of a body includes a collapsible basket in a narrow sheath. A surgeon advances the device beyond an object to be removed from a body, such as a kidneystone, a gallstone, or a thrombus. The surgeon then retracts the sheath or advances the basket from the sheath. The basket deploys only to one side of the sheath. In some embodiments, the periphery of the basket has a flex point to enable the basket to easily collapse into the sheath. If the sheath is adjacent a body vessel, such as a blood vessel or a ureter, the sheath remains adjacent the wall, while the device deploys in such a manner as to seal against the walls of the vessel and block the flow of fragments, emboli, thrombi, or other undesirable objects.

Abstract: A sampling apparatus for taking a sample from the body of a patient is easily rotatable while the sample is being taken. This allows the physician to aspirate or draw the sample, rotating the sampling apparatus while holding stationary a syringe or other container for receiving the sample.

Abstract: An embryo transfer catheter with a protective sheath is disclosed. The use of a protective sheath shields a guide catheter from cervical mucus. The retracted open flaps of the outer protective sheath draw the mucus and blood away from the inner guide catheter. This allows an inner embryo transfer sheath to enter the uterus unobstructed. The embryo is then transferred to the uterus by means of fluid pressure with a culture medium. The protective sheath may be snap fit onto the guide catheter. The sheaths and catheters may be manufactured in a variety of lengths for individual convenience and then snap-fit onto each other for better control during an embryo implantation procedure. Other catheters and related instruments may also be manufactured with snap-on features.

Abstract: Double ended wire guides are manufactured so that either end, or both ends sequentially, may be inserted into a patient. The ends are different, so that the inventory requirements of wire guides are minimized. For example, a wire guide may have a straight end and an angled end, either end suitable for use on the patient. The wire guides may also differ in other characteristics, such as the stiffness or the diameters of the distal and proximal portions. The wire guide may also be stored in a package, the package including a fitting so that wetting solution may be injected into the package to wet the wire guide and prepare it for use.

Abstract: A stent is made from a coiled wire and is very smooth along its length and as well its ends. The stent is thus highly atraumatic to patients, and because of its smooth surfaces, it presents a surface to which it is difficult for microbes to cling. The stent may be used in a minimally invasive procedure, such as for a ureteral stent, and may also be used percutaneously. Similar stents may be used in other body areas, such as in draining the biliary tract, the gastro-intestinal tract, hepatic procedures, and in vascular procedures as well.

Abstract: A positioner is provided that is able to precisely position a stent, such as a ureteral stent, by using an anatomical landmark, such as a ureteral orifice. The positioner is placed over a wire guide and advanced until the proximal portion of the stent abuts a stent-stop. The positioner and stent are together pushed until the positioner reaches the ureteral orifice. The stent can be deployed and the positioner can be removed leaving the stent correctly positioned within the kidney and bladder.

Abstract: A rigid extractor is revealed, a rigid device for use in percutaneous procedures to remove kidney stones directly from the kidneys. The rigid extractor uses a handle fixed to an outer rigid cannula, and an inner cannula to control an extraction device that may be removable from the inner cannula. The extractor is desirably used with a fluoroscope, in which the surgeon maneuvers the extractor with the aid of a view of the operating field provided by the fluoroscope. The surgeon then maneuvers the extractor to grasp the kidney stones and remove from the patient. The extractor may also be used with a nephroscope. The device may be used with a removable extraction device such as a basket, a grasper a pair of jaws, or a pair of scissors.

Abstract: An incubation condition monitoring device has at least one reader unit (10) to measure selected characteristics with an incubator (2). The reader unit transmits the information to a receiver/transmitter (12) within the incubator to receive the measurements and to transmit the measurements of the selected characteristics to a data logger (14) outside the incubator. A monitor and display system (16) monitors and displays the measurements of the selected characteristics. The selected characteristics within the incubator can be temperature and pH.

Abstract: A removable and replaceable handle for a medical device includes a main body with a distal end, a proximal end, and a longitudinal axis between the distal and proximal ends and a slider disposed within the main body that is translatable along the longitudinal axis between the distal and proximal ends. A first gripper is disposed within the slider and a second gripper is disposed within the main body, which are capable of retaining a control portion of the medical device when the slider is in the first position with a working portion of the medical device in a biased position, and allows the medical device to be removed from or inserted into the handle when the slider is in the second position.

Abstract: A graft and method of using a graft are described that should decrease the incidence of abnormal placentation and uterine rupture that result from cesarean section and restore the anatomic integrity of the uterus at a hysterotomy surgical site, while not disturbing the involution of the postpartum uterus.

Abstract: A device for use in culturing a cell is provided. The device comprises at least one cell culture chamber and a fluid reservoir. The cell culture chamber has a tapered side wall and is in fluid connection with the fluid reservoir via a fluid path which is connected to the culture chamber via an aperture in the culture chamber. The aperture is smaller than the diameter of the cell to be cultured such that the cell is maintained within the cell culture chamber.

Abstract: A medical device having a bioactive in a salt and a free-base form contained within the device and/or coated onto a surface of the device. The salt and the free-base form have different solubilities in an aqueous medium. The elution of bioactive from the device in an aqueous medium is tailored by fixing the ratio of forms. Methods of preparing such a device are also provided.

Abstract: A prosthetic testicle is provided that is able to mimic the movement and feel of a natural testicle while at the same time being able to remodel itself into native tissue. Additionally, the prosthetic testicle is able to provide long-term delivery of drugs into the patient.

Abstract: A single device is provided for performing the diagnostic procedures of sonohysterography and endometrial biopsy. The device includes a cervical seal to occlude the cervix and a substance delivery and removal device to deliver and remove a fluid from the uterus. The substance delivery and removal device may also be used to create a vacuum so that suction occurs near side-ports that are used to collect endometrial tissue samples from multiple locations as the device is rotated or moved laterally within the patient. Additionally, the sample may be taken using a cellular collection device.

Abstract: A single device is provided for performing hysterography and intrauterine venography having a marker that aids in positioning the device within the patient, having a bulb-tip to seal the cervix, having a bulb-tip opening to allow an image enhancing medium to be discharged from a needle and injected into the uterus to perform the hysterography, having a needle to discharge and inject an image enhancing medium into the fundal myometrium to perform the intrauterine venography, and having a needle securing mechanism to secure the needle to prevent patient injury during transcervical introduction of the device.

Abstract: A kit and method for supporting a pelvic floor of a person with stress urinary incontinence or other symptoms. The method involves using barbed sutures as part of a sling for supporting the pelvic floor or urethra of a person experiencing stress urinary incontinence or other symptoms. A surgeon implants the sling along with the barbed sutures, using one of several known methods. The barbed sutures may be interwoven with the sling and the supports for the sling, so that once the sling and its supports are placed into the patient, barbs of the sutures will resist movement. The sutures may also be woven into the supports to resist movement.