Abstract: A chemical analyzer includes a slide transport mechanism having a slide track adapted to hold a plurality of reagent test slides, a sample metering device, an incubator formed as a part of the slide transport mechanism to precisely maintain the temperature of the reagent test slides, a slide ejector mechanism to remove the slides from the slide transport mechanism, a sample preparation station, which includes a centrifuge, and associated electronics and software. The slide transport mechanism holds a plurality of trapezoidally-shaped reagent test slides about its circumference, which slides are loaded onto the transport mechanism by the slide inserter mechanism. The slide transport mechanism positions the reagent test slides under the sample metering device, which device deposits a predetermined volume of sample onto each slide. The slide transport mechanism also carries the slides above a reflectometer.

Abstract: An anticoagulant-coated dipstick is selectively receivable by the central fill port of a rotor of a blood centrifuge. The dipstick includes an elongated, rod-like member having a first axial end and an opposite second axial end, and a cap affixed to the second axial end. At least a portion of a surface of the rod-like member is coated with an anticoagulant. The elongated rod-like member of the dipstick is dimensioned in length and diameter to be receivable through the central fill port of the rotor to contact a blood sample contained therein. The cap is circular in shape, with a diameter that is greater than that of the rotor fill port to entirely cover and seal the fill port to prevent leakage therethrough of a blood sample contained in the rotor, especially when the rotor is gently agitated or inverted.

Abstract: A chemical analyzer includes a slide transport mechanism having a slide track adapted to hold a plurality of reagent test slides, a sample metering device, an incubator formed as a part of the slide transport mechanism to precisely maintain the temperature of the reagent test slides, a slide ejector mechanism to remove the slides from the slide transport mechanism, a sample preparation station, which includes a centrifuge, and associated electronics and software. The slide transport mechanism holds a plurality of trapezoidally-shaped reagent test slides about its circumference, which slides are loaded onto the transport mechanism by the slide inserter mechanism. The slide transport mechanism positions the reagent test slides under the sample metering device, which device deposits a predetermined volume of sample onto each slide. The slide transport mechanism also carries the slides above a reflectometer.

Abstract: An anticoagulant-coated dipstick is selectively receivable by the central fill port of a rotor of a blood centrifuge. The dipstick includes an elongated, rod-like member having a first axial end and an opposite second axial end, and a cap affixed to the second axial end. At least a portion of a surface of the rod-like member is coated with an anticoagulant. The elongated rod-like member of the dipstick is dimensioned in length and diameter to be receivable through the central fill port of the rotor to contact a blood sample contained therein. The cap is circular in shape, with a diameter that is greater than that of the rotor fill port to entirely cover and seal the fill port to prevent leakage therethrough of a blood sample contained in the rotor, especially when the rotor is gently agitated or inverted.

Abstract: A ureteral stent for assisting movement of urine along a patient's ureter and into the patient's bladder. The stent includes an elongated tubular segment extending toward the bladder from a kidney end region for placement in the renal cavity to a bladder end region. A central lumen connects at least one opening at the first end region to at least one opening in the bladder end region. Thin flexible tail(s) are attached to the bladder end region of the tubular segment at a point outside the bladder so as to receive urine from the opening in the bladder end region and to transport urine from there across the ureter/bladder junction and into the bladder. The tails include an elongated external urine-transport surface configured to transport urine. The transporting surface(s) are configured to extend along at least part of the ureter, across the ureter/bladder junction, and into the bladder.

Abstract: A ureteral stent for assisting movement of urine along a patient's ureter and into the patient's bladder. The stent includes an elongated tubular segment extending toward the bladder from a kidney end region for placement in the renal cavity to a bladder end region. A central lumen connects at least one opening at the first end region to at least one opening in the bladder end region. Thin flexible tail(s) are attached to the bladder end region of the tubular segment at a point outside the bladder so as to receive urine from the opening in the bladder end region of the tubular segment and to transport urine from there across the ureter/bladder junction and into the bladder. The tails include an elongated external urine-transport surface sized and configured to transport urine along the ureter. The urine transporting surface(s) are sized and configured to extend along at least part of the ureter, across the ureter/bladder junction, and from there into the bladder.

Abstract: A ureteral stent for assisting movement of urine along a patient's ureter and into the patient's bladder. The stent includes an elongated tubular segment extending toward the bladder from a kidney end region for placement in the renal cavity to a bladder end region. A central lumen connects at least one opening at the first end region to at least one opening in the bladder end region. Thin flexible tail(s) are attached to the bladder end region of the tubular segment at a point outside the bladder so as to receive urine from the opening in the bladder end region of the tubular segment and to transport urine from there across the ureter/bladder junction and into the bladder. The tails include an elongated external urine-transport surface sized and configured to transport urine along the ureter. The urine transporting surface(s) are sized and configured to extend along at least part of the ureter, across the ureter/bladder junction, and from there into the bladder.

Abstract: A blood collection bag assembly is provided. The assembly includes a flexible blood collection bag, a length of flexible tubing extending from and communicating with the bag and a connector secured to the end of the flexible tubing remote from the bag. The connector includes a needle pierceable resealable closure secured in sealing engagement with the end of the flexible tubing remote from the bag. The connector can be used with a conventional needle holder, such as the type used to collect specimens of blood into an evacuated tube. The blood collection bag assembly has no sharp components, and hence is safe and easy to use. Additionally, the blood collection bag assembly can be used with conventional evacuated tubes to avoid cut and drip techniques for collecting specimens of blood for analysis.

Abstract: A ureteral stent for assisting movement of urine along a patient's ureter and into the patient's bladder. The stent includes an elongated tubular segment extending toward the bladder from a kidney end region for placement in the renal cavity to a bladder end region. A central lumen connects at least one opening at the first end region to at least one opening in the bladder end region. Thin flexible tail(s) are attached to the bladder end region of the tubular segment at a point outside the bladder so as to receive urine from the opening in the bladder end region of the tubular segment and to transport urine from there across the ureter/bladder junction and into the bladder. The tails include an elongated external urine-transport surface sized and configured to transport urine along the ureter. The urine transporting surface(s) are sized and configured to extend along at least part of the ureter, across the ureter/bladder junction, and from there into the bladder.

Abstract: In an aspect, the invention relates to an instrument for obtaining tissue samples from a site deep within the body. The instrument has an elongated proximal portion that is constructed to follow a long, torturous path to the site and has a distal end constructed to sever and remove a tissue sample from the body, including tissue specimens, polyps or the like. The improvement includes that the instrument is constructed to take multiple biopsy samples without being withdrawn from the body. The instrument includes a tissue sample retractor. The retractor is axially movable between an extended tissue-engaging position and a retracted position. There is an open passage into which the retractor moves when moving from the extended to the retracted position. The retractor has a distal end portion constructed to engage tissue and apply axial transporting force thereto while moving from the extended to the retracted position.

Abstract: A laser lancet tip and method for controlling laser incisions for the purpose of taking blood samples from patients in a variety of body locations and age groups. A removable tip on a laser is used to mask a laser pulse and modify the length and width of an incision made by the laser by only allowing a portion of the laser beam to contact the target surface. The depth of the incision may be controlled by either a lens or filter which is optically aligned with the laser beam.

Abstract: The invention features a device for obtaining tissue samples from a site deep within the body having a proximal portion constructed to follow a long torturous path to the site and a distal portion constructed with a jaw arrangement that can be opened and closed to sever a sample, including tissue specimens, polyps and the like, from the surface. The device is constructed for severing and storing at least three successive samples. The device includes a sample storing and retaining element in the space encompassed by the jaws. The element is fixed to maintain an orientation extending generally distally along a selected length to a distal end and has a profile along the length for engaging multiple samples arranged axially in the order in which they were severed from the surface with sufficient frictional force to substantially retain the samples from moving distally from the space encompassed by the jaws when the jaws are opened to sever a successive sample from the surface.

Abstract: A non-rotational catheter clamp. The clamp comprises a snap-acting device which contains a rotatable inner and outer member. The inner member has an inner passageway for a catheter and an outer surface containing at least one protrusion. The outer member has an interior beveled sidewall. When the outer member is twisted or rotated in a first direction relative to the inner member, the protrusion on the inner member is compressed by the beveled sidewall, thereby compressing the inner member and the catheter. When the outer member is twisted in the opposite direction relative to the inner member, the protrusion disengages from the beveled sidewall and the catheter is decompressed. Use of the clamp in conjunction with a catheter contamination sleeve is disclosed.

Abstract: A catheter clamp. The clamp comprises a snap-acting device which contains a rotatable inner and outer member. The inner member has an inner passageway for a catheter and an outer surface containing at least one protrusion. The outer member has an interior beveled sidewall. When the outer member is twisted or rotated in a first direction relative to the inner member, the protrusion on the inner member is compressed by the beveled sidewall, thereby compressing the inner member and the catheter. When the outer member is twisted in the opposite direction relative to the inner member, the protrusion disengages from the beveled sidewall and the catheter is decompressed. Use of the clamp in conjunction with a catheter contamination sleeve is disclosed.

Abstract: Large diameter catheters for drainage of body cavities and infusion are disclosed. A removable assembly comprising a stiffening cannula, hollow dilator and wire guide facilitate insertion, reduce trauma and reduce the risk to delicate tissue. The distal tip of the stiffening cannula interfaces with a shoulder within the catheter adjacent to the tip, and insertion is accomplished by application of axial pressure on the cannula which is transmitted to the catheter via the shoulder. The tapered tip of the dilator conforms to and reinforces the pliant tip of the catheter during insertion. The catheter includes a branch line for infusion and sampling.