Abstract: A vascular catheter embedded with a radiopaque material providing a distinct, non-physiological pattern that may be easily detected on a radiograph. The radiopaque material may be embedded within the wall of the catheter in an open wound, helical formation. Detection of the catheter by x-ray is increased due to the non-physiological radiograph pattern and due to the increased presence of the radiopaque material. The non-physiological formation increases the radiopacity of the catheter, yet requires less radiopaque material than traditional radiopaque catheters. The non-physiological formation and decreased amount of radiopaque material provides for a more detectible and less rigid catheter that is resistant to kinks and occlusions.

Abstract: The present invention provides a catheter for extraction that can efficiently extract blood flowing in coronary sinus from coronary artery through coronary vein and has the same operability as catheters used in conventional PCI. The present invention also provides a catheter for extracorporeal circulation that can lessen an introduction number of devices for blood access as little as possible and reduce further the burden to a patient, in addition to the same operability as the catheters used in the conventional PCI. The catheter for extraction is equipped with blood extracting lumen in an inside and equipped with a hub at a proximal end portion, and when a minimum sectional area to a circumferential direction of the blood extracting lumen is referred to as S1 and immersion side length is referred to as L1, an equivalent diameter D1 satisfies the formula defined by D1=(4×S1)/L1 and the equivalent diameter D1 is at 1.80 mm.

Abstract: An implantable medical device includes, according to one embodiment, at least one radiopaque and MRI-compatible component comprising an oxide dispersion strengthened metal alloy, where the oxide dispersion strengthened metal alloy has a volume magnetic susceptibility of no greater than about 100×10?6 and a radiopacity greater than that of grade 304 stainless steel.

Abstract: The present disclosure is directed a method of facilitating treatment via a vascular wall defining a vascular lumen containing an occlusion therein. The method may include providing a first intravascular device having a distal portion and at least one aperture and positioning the distal portion of the first intravascular device in the vascular wall. The method may further include providing a reentry device having a body and a distal tip, the distal tip having a natural state and a compressed state and inserting the distal tip, in the compressed state, in the distal portion of the first intravascular device. The method may further include advancing the distal tip, in the natural state, through the at least one aperture of the first intravascular device.

Abstract: A nasogastric tube placement and monitoring system is provided including a flexible nasogastric tube and numerous circuits that can be used alone or in combination. The circuits include a feedback initiator, a feedback receiver, and a clinician notifying device. By various means in the provided circuits, the feedback initiator provides information about the location of the distal end of the nasogastric tube. This information or data is received and analyzed by the feedback receiver that monitors the circuit, which then transmits an output to the clinician notifying device to alert or advise the attending clinician of this information. The data that is output supplies information about the location of the tube's distal end to the clinician, thereby assisting the clinician in placement of the nasogastric tube during intubation, as well as in monitoring proper tube placement after placement.

Abstract: An imaging system includes a display, an x-ray based image acquisition device, a workstation, and a medical device, e.g., a catheter. The image acquisition device is configured to obtain real-time two-dimensional images of a portion of a patient's body that is disposed within the field of view of the image acquisition device. The workstation is configured to integrate and register a three-dimensional model of an anatomic structure with the two-dimensional image, and to provide the display with a real-time image of the integrated image. The catheter includes a distal portion that comprises a radiopaque material. The image acquisition device is further adapted to apply radiation at a first dosage rate that is below a second dosage rate sufficient to detect anatomic structures.

Abstract: A steering mechanism (10) for a catheter includes tubular member (12) defining passage (14). The tubular member (12) has longitudinally extending, bend-enhancing portion (18) formed at predetermined region of the tubular member (12). Actuator (16) is received in the passage (14) of tubular member (12), distal part (16.2) of actuator (16) being fast with a distal part (20) of the tubular member (12).

Abstract: A site marker deployment device includes a housing defining a first portion, an outer cannula at least partially interposed within the first portion and having a proximal end and a distal end defined by an outer cannula aperture, an inner member at least partially interposed within the outer cannula, a first biasing portion, a second biasing portion, wherein the second biasing portion will selectively urge the outer cannula to move proximally relative to the inner member, and a site marker selectively disposed within the outer cannula adjacent the inner member, near the distal end of the outer cannula. The first biasing portion will selectively urge a site marker at least partially within the outer cannula.

Abstract: This invention is new apparatuses and methods for treatments to be used from inside conduits or biological pathways. Examples of the biological pathways in which these new apparatuses and methods may be used include arteries, veins, and respiratory ways. Multi-purpose catheters (10) and catheter systems using structures including wires (2108), balloons (2150), and cords (2204) are described as well as methods to use such catheters and catheter systems. One of the embodiments is a configurable wire system which carries or transports radioactive sources. The wire is used in conjunction with a closed-end channel catheter.

Abstract: The therapeutic catheter comprises a lumen communicating from the user's side end to the terminal tip part thereof, a main shaft having, at its tip, a guide wire lumen, a hub at its user's side end, and a slit in the guide wire lumen through its entire length, or the therapeutic catheter comprises a main shaft having a lumen communicating from the user's side end to the terminal tip part thereof, a guide wire shaft having, at its tip, a guide wire lumen, a hub at the user's side end of the main shaft, and a slit in the guide wire shaft through its entire length. The guide wire or the shaft of the other catheter playing the role of the guide wire can be rapidly disposed in the guide wire lumen through the slit.

Abstract: The invention is directed to a self-expanding stent for implantation into a body lumen, such as an artery. The stent consists of a plurality of radially expandable cylindrical elements generally aligned on a common longitudinal stent axis and interconnected by a plurality of interconnecting members placed on the stent in a collinear arrangement such as to create at least one continuous spine which extends along the length of the stent. The invention is also directed to a stent delivery system for implantation of a stent in a vessel which includes an outer tubular member having a restraining sheath and an inner tubular member having a distal end which has a compressed stent mounted thereto. The proximal end of the inner tubular member is connected to a housing assembly which prevents the inner tubular member from moving when the outer tubular member is retracted to deploy the stent.

Abstract: Medical devices with radiopaque markers, and related systems and methods are disclosed.

Abstract: A delivery system for implanting a medical device into the body of a patient or subject and a method of use thereof. The delivery system includes a delivery catheter having a catheter lumen and an inner member extending therethrough. The inner member includes a distal tip portion, a proximal portion, and an intermediate portion, the intermediate portion being disposed adjacent to the distal end of the delivery catheter. A first sealing member, positioned near a distal end of the proximal portion, forms a fluid seal between the inner member and an inside surface of the delivery catheter. A second sealing member, positioned near a proximal end of the distal tip portion, forms a fluid seal between the inner member and an inside surface of the delivery catheter. The intermediate portion extends between the first seal and the second seal. In one embodiment, a medical device and a hydrating fluid are present in a device-containing region between the intermediate portion and the delivery catheter.

Abstract: A method and apparatus for delivering a medicine to a patient via the patient's respiratory system with control and efficiency. A nebulization catheter is positioned in the patient's respiratory system so that a distal end of the nebulization catheter is in the respiratory system and a proximal end is outside the body. In a first aspect, the nebulization catheter may be used in conjunction with an endotracheal tube and preferably is removable from the endotracheal tube. The nebulization catheter conveys medicine in liquid form to the distal end at which location the medicine is nebulized by a pressurized gas or other nebulizing mechanism. The nebulized medicine is conveyed to the patient's lungs by the patient's respiration which may be assisted by a ventilator. By producing the aerosol of the liquid medicine at a location inside the patient's respiratory system, the nebulizing catheter provides for increased efficiency and control of the dosage of medicine being delivered.

Abstract: An elongated sheath of a guide catheter includes a fully radiopaque and echogenic distal tip having a length greater than approximately 0.08 inch.

Abstract: A forwardly directable fluid jet crossing catheter having a positionable jet body which can be longitudinally and rotationally positioned in order to direct a fluid jet stream to impinge, break through, and cross a chronic total occlusion. The distal end of the catheter includes a tip of super-elastic material having a flexible bend aligned within the distal portion of a sheath which tip is directable in response to the longitudinal and rotational orientation of a positionable jet body, whereby a fluid jet stream can be controlled in angular and rotational directions.

Abstract: A system is provided that includes an elongated introducer navigable through body vessels of a human subject and a pusher component for incorporation within the introducer. The pusher component includes a tubular portion with a spiral ribbon. A radiopaque marker is secured to at least a portion of the spiral ribbon such that an outer surface of the radiopaque marker is substantially flush with an outer surface of the tubular portion immediately proximal and/or immediately distal the radiopaque marker. According to a method of manufacturing such a component, the spiral ribbon is formed by a spiral cutting operation and a pre-assembly radiopaque marker member is crimped onto the spiral ribbon. According to another method of manufacturing such a component, the spiral ribbon is formed by winding a filament and a pre-assembly radiopaque marker member is crimped onto the spiral ribbon.

Abstract: Real-time, enhanced imaging of remote areas, too minute for CT imaging, is made possible through a probe having a radiopaque tip as well as radiopaque volume markers. When deployed, the markers outline the space containing the tip such that both the tip and the volume containing the tip are viewable on a fluoroscope. This device may be used in conjunction with or independently of 3-D volumes created from CT scans and 3-D tip sensors.

Abstract: A method of determining a position of a second object which travels along a first object. The method comprising determining a position for a first object; determining a linear displacement of a second object relative to the first object; and ascertaining a position of said second object based upon said relative linear displacement and said position of said first object.

Abstract: Medical devices and methods for making and using the same. An example medical device may include an elongate shaft having a proximal region and a distal region. A tubular member may be disposed over the distal region of the shaft. The tubular member may have an outer surface and may have a plurality of slots formed therein. A coil may be disposed adjacent the tubular member.

Abstract: Constructive disposal placed in artifon catheter applied in perforations above the papillae in fistula-papillotomy, where the procedure known as Endoscopic Retrograde Cholangiopancreatography (ERPC) is characterized by the combination of instrumental transpapillary access and the obtaining of contrasting images through pancreatic bile, a result obtained through the use of the artifon catheter device (A) claimed herein, which regards a perforation catheter above the papilla in fistula-papillotomy, to obtain access to biliary passages, making way for an alternative to known surgical techniques, this artifon catheter device (A) presenting a constructive concept composed of a Y connector component (1); a manipulating component of the concentric perforating tube (2); an external concentric tube component (3), within which a concentric perforation tube component (4) is located of which the far end is connected to a needle component (5); radiopaque marks components (6); a manipulating component of the external conce

Abstract: A radiopaque marker configured for being securing to a tubular member adapted for introduction into a patient and having relief sections to provide localized accommodation of diametrical-circumferential dimensional reduction.

Abstract: Devices and methods for exploiting intramural (e.g., subintimal) space of a vascular wall to facilitate the treatment of vascular disease, particularly total occlusions. For example, the devices and methods disclosed herein may be used to visually define the vessel wall boundary, protect the vessel wall boundary from perforation, bypass an occlusion, and/or remove an occlusion.

Abstract: Medical catheters adapted for use within a body vessel and methods of manufacturing are presented herein. The medical catheter comprises a tubular catheter shaft having a distal end that fits within the body vessel. The tubular catheter shaft comprises an unfilled or low-loaded inner liner and/or outer shell. The medical catheter also comprises a radiopaque segment that comprises a radiopaque material embedded between the inner liner and outer shell. The radiopaque material can be in the form of an ink, powder, or paste.

Abstract: A method for forming electrically conductive patterns to provide an electrically conductive path on a polymer tube is provided. The method includes the steps of establishing a polymer tube and mounting such in a displaceable and rotatable mounting that is adapted to provide both axial and rotational motion. This is followed by forming at least one channel having a predetermined pattern in the polymer tube with a focused energy beam, the channel then being filled with an electrically conductive paste or electrically conductive slurry material. The polymer tube is then heated to temperatures less than 250° C. to cure the electrically conductive paste or electrically conductive slurry material. The electrically conductive paste or electrically conductive slurry material is then covered with a polymer layer.

Abstract: A catheter, including: a reinforced tube including a plurality of concentric bonded tubular layers of non-radiopaque material and a radiopaque, coil spring captured between adjacent ones of the tubular layers, one end of the reinforced tube providing an annular mounting portion and a tubular mounting member extending outwardly of the annular mounting portion; and a tapered tip of radiopaque material including a tip central portion providing a tip central passageway receiving the tubular mounting member and a tip mounting portion abutting and bonded to the annular mounting portion, the tip central portion bonded to the tubular mounting member.

Abstract: Various improved catheter marking arrangements are described. In a first aspect of the invention, a first longitudinally extending radiopaque marker is positioned on the catheter. A second longitudinally extending radiopaque marker is positioned opposite the first marker at a rotational orientation that is approximately 180 degrees offset from the first marker. The second marker has a length that is sufficiently different from the first marker such that a surgeon utilizing the catheter in a surgical procedure would be able to readily differentiate the first and second markers in a fluoroscopic image based on their respective lengths in order to determine the rotational orientation of the catheter. In some embodiments, the catheter includes a lumen that has a side port that opens to a side of the catheter. The first marker is composed of a pair of axially aligned marker segments located on opposite ends of the side port.

Abstract: The medical tube inserted into a body cavity of a patient includes a flexible tube and a magnet provided at the tip end portion of the tube for electromagnetically detecting the position of the tip end portion of the tube inserted in the body cavity, from outside the body. This magnet includes a plurality of magnet pieces arranged in the length direction of the tube to have a column-like shape as a whole. The direction of magnetic pole of the magnet is set to the length direction of the tube. Therefore, since the magnet is divided into a plurality of magnet pieces, even a magnet increased in size can be inserted smoothly into a body cavity of a patient.

Abstract: An intracorporeal catheter, such as a guiding catheter, employed for intraluminal procedures is disclosed. The catheter generally has an elongated catheter shaft including a polymeric inner layer and a non-radiopaque outer polymeric layer, along with a radiopaque reinforcing structure disposed between the inner and outer layers. In one embodiment, the reinforcing layer consists of multiple drawn filled tubes braided or wound together. The drawn filled tubes may have a stainless steel outer jacket clad over a radiopaque inner core, or the drawn filled tubes may have a radiopaque outer jacket clad over a stainless steel core. In another embodiment, the reinforcing layer may consist of multiple wires containing radiopaque alloys braided or wound together, wherein at least two of the wires consist of different radiopaque alloys. The strands of the reinforcing structure may have a circular or a rectangular transverse cross-sectional shape.

Abstract: High radiopacity is achieved in a polymeric marker by combining a polymeric resin, a powdered radiopaque agent having uniformly shaped particles of a specific particle size distribution and a wetting agent. The method to produce the marker calls for the blending and pelletization of these materials followed by extrusion onto support beading. The resulting supported tubing is subsequently cut to length with the beading still in place. After ejection of the beading remnant the marker is slipped into place on the device to be marked and attached by melt bonding. Marking of a guidewire allows lesions to be measured while the marking of balloon catheters allow the balloon to be properly positioned relative to a lesion.

Abstract: A method of performing a medical procedure is disclosed which involves the use of a balloon catheter in combination with an angioscope to monitor an intravascular stent before, during or after deploying the stent. Specifically, the method may include the steps of (1) delivering an intravascular stent into the vasculature of a patient, (2) positioning a balloon catheter in the vasculature such that the inflatable balloon is adjacent the stent, (3) inserting an angioscope into the balloon catheter such that the distal end of the angioscope is adjacent an optically-transparent tube traversing the interior of the balloon, and (4) visually monitoring the stent before, during or after deploying the intravascular stent. The optically-transparent tube may define a guide wire lumen for use with a guide wire and the angioscope may be inserted into the guide wire lumen. The intravascular stent may be a balloon-expandable stent, a self-expanding stent, or a stent made of a photo-responsive polymer.

Abstract: Apparatus and methods for regulating the appetite of an individual suffering from morbid obesity, the apparatus including a plurality of stimulation electrodes arranged longitudinally on at least one electrode support shaft for insertion within the hypothalamus for outputting electrical discharges to specific sites within the hypothalamus. Each of the plurality of stimulation electrodes may be independently controlled. Electrical discharge of various frequencies transmitted from one or more of the plurality of stimulation electrodes, and delivered to a region of the hypothalamus that is involved with either stimulating or inhibiting appetite, may be used to regulate appetite in the individual. Alternatively, an individual's appetite may be regulated by the microinfusion from at least one microinfusion catheter of an appropriate quantity of a suitable drug to a distinct site or region within the hypothalamus.

Abstract: Compound steering assemblies, usable in both diagnostic and therapeutic applications, enable a physician to swiftly and accurately steer the distal section of the catheter in multiple planes or complex curves to position and maintain ablation and/or mapping electrodes in intimate contact with an interior body surface.

Abstract: A handle for a medical device is provided. The handle includes an inner handle member and first and second outer handle members slideably disposed on the inner handle member. An elongate sheath is attached to the inner handle member and extends axially beyond a distal end of the inner handle member and a stylet is attached to one of the outer handle members and disposed in a lumen of the sheath. Slideable movement of the outer handle members relative to the inner handle members controls relative positioning of various components of the handle.

Abstract: A catheter assembly comprises a catheter shaft having a first region and a second region. The first region is less radiopaque than the second region. The first region is constructed of a shaft material and the second region is constructed from the shaft material in combination with at least one radiopaque material. At least a portion of the shaft material of the second region defines at least one grooved region. The at least one radiopaque material is positioned at least partially within the at least one grooved region.

Abstract: An echogenic and/or radio-opaque device adapted to permit carrying out removals from the genital organs for analysis, or adapted to promote the transfer of products, particularly gametes or embryos, into the female genital organs, or again adapted to carry out tests for the introduction of catheters into the uterus and to analyze the morphology of the neck of the uterus and of the uterine cavity. The device comprises an echogenic and/or radio-opaque material permitting visualizing by medical imagery, particularly by echography or radiography, the position of the usable orifice or of the distal portion of the device.

Abstract: The present invention is directed to apparatus and methods for treating a vascular occlusion by providing an infusion catheter having an atraumatic tip and at least one delivery port configured to infuse fluid into the occlusion. The fluid that is infused dilutes the occlusion and reduces adhesion of the occlusion to an intima of the vessel wall, thereby causing the occlusion to dislodge. Emboli generated in the process are directed into an emboli removal catheter for removal.

Abstract: Disclosed is a catheter for penetrating a stenotic lesion occurred in a lumen in a human body, including:

Abstract: A tubular medical catheter having a least one region of selectively varied lamination is provided herein.

Abstract: A carrier catheter (20) for the introduction and positioning or changing of one or more guidewires (GW1, GW2, GW3) or interventional devices in a vessel V in the body of a subject. The catheter (20) includes an elongated, thin flexible body (22) having a primary lumen (24) and ancillary lumens (26, 28). Each lumen has an opening at the proximal end and an opening (30, 32, 34) at the distal end to permit a guidewire or device to extend through and exit the lumen. The openings at the distal ends of the lumens are positioned so that the respective guidewires or interventional devices can exit the lumens at different locations along the distal end of the catheter. One introduction of the device allows the deployment of any combination of multiple guidewires and interventional devices. The catheter can be used for a rapid replacement of an indwelling catheter or rapid replacement of a dedicated guidewire.

Abstract: A microdialysis probe includes a dialysis membrane located and supported between a closed distal end of the probe and a proximal end of the same, which membrane essentially-surrounding a space for passage of perfusion liquid. The probe has an inlet and outlet for perfusion liquid. The probe exhibits a deformable mesh sleeve adapted to enclose and protect at least the dialysis membrane, the proximal end of the deformable being fastened to the probe between the proximal end of the probe and the dialysis membrane.

Abstract: A handle includes a body portion and a handle portion which is slidably and rotatably mounted on the body portion. Shoulders on the body portion and the handle portion limit relative sliding movement of the body portion and handle portion. A catheter open at both ends has one end fixed to the handle portion for movement therewith, the opposite end of the catheter having a shape memory tip. A fitting is threadedly connected to an enlarged part of the body portion. A sheath is threadedly connected to the fitting and the catheter is slidable and rotatable within the sheath. An annular channel is provided between the sheath and the catheter, this channel being in fluid communication with a bore in the fitting. The outer end of the sheath has holes therethrough in fluid communication with the channel. An irrigation inflow and aspiration outflow tube is also in fluid communication with the bore in the fitting.

Abstract: A container for irradiation of blood products comprises a flexible, flat collapsible wall defining a sealed blood product chamber, the plastic material of said wall being substantially transparent to the irradiation, which is typically ultraviolet radiation. An access port or ports are provided for communicating through the wall to the blood product chamber. A flap is provided, integral with the wall and spaced from the chamber. The flap carries identifying indicia including a typically bar code indicia, so that the wall which defines the blood product chamber may be at least substantially free of opaque indicia. Also, means may be provided for detecting an indicating exposure of the container to such irradiation, such as ultraviolet sensitive tape adhering to the flap. Alignment holes may be provided, typically in the flap, to facilitate the orientation of the container with apparatus for irradiation and apparatus for bar code reading, making use of alignment pins carried by such apparatus.

Abstract: Medical catheters adapted for use within a body vessel and methods of manufacturing are presented herein. The medical catheter comprises a tubular catheter shaft having a distal end that fits within the body vessel. The tubular catheter shaft comprises an unfilled or low-loaded inner liner and/or outer shell. The medical catheter also comprises a radiopaque segment that comprises a radiopaque material embedded between the inner liner and outer shell. The radiopaque material can be in the form of an ink, powder, or paste.

Abstract: A handle includes a body portion and a handle portion which is slidably and rotatably mounted on the body portion. Shoulders on the body portion and the handle portion limit relative sliding movement of the body portion and handle portion. A catheter open at both ends has one end fixed to the handle portion for movement therewith, the opposite end of the catheter having a shape memory tip. A fitting is threadedly connected to an enlarged part of the body portion. A sheath is threadedly connected to the fitting and the catheter is slidable and rotatable within the sheath. An annular channel is provided between the sheath and the catheter, this channel being in fluid communication with a bore in the fitting. The outer end of the sheath has holes therethrough in fluid communication with the channel. An irrigation inflow and aspiration outflow tube is also in fluid communication with the bore in the fitting.

Abstract: A central venous catheter is provided having a proximal tube segment, a distal tube segment and a transition tube segment interposed between the proximal and distal tube segments which are preferably formed as a single integrated tube containing polymer material of different durometer and varying amounts of radiopaque filler material. The polymer durometer of the proximal segment is higher than the polymer durometer of the distal segment. By contrast, the percentage by weight of the filler material contained in the distal segment is higher than that of the proximal segment. The variation in the polymer durometer and the filler amount along the length of the tube provide the desired tensile strength, hardness, chemical resistance and fatigue resistance at the proximal segment and at the same time provide the desired flexibility and radiopacity at the distal segment.

Abstract: A catheter assembly comprises a catheter shaft having a first region and a second region. The first region is less radiopaque than the second region. The first region is constructed of a shaft material and the second region is constructed from the shaft material in combination with at least one radiopaque material. At least a portion of the shaft material of the second region defines at least one grooved region. The at least one radiopaque material is positioned at least partially within the at least one grooved region.

Abstract: A catheter having one or more radio-opaque bands near the distal end is designed to be inserted into the renal artery so that the distal end of the catheter is adjacent to the origin of the renal artery. An X-ray image of the bands is used to position the X-ray head relative to the aorta and renal artery so that a useful, unobstructed radiological image perpendicular to the axis of the renal artery at its origin is obtained. This facilitates the positioning of a stent in the renal artery so that the stent encompasses the origin and extends no more than about three millimeters into the aorta. Two radio-opaque bands placed close to one another define a narrow radio-translucent band such that when the X-ray head is rotated to a position where parallax is reduced and the radio-translucent band can be imaged, the renal artery can be appropriately imaged without being obscured by the aorta.

Abstract: A tissue penetrating catheter that is usable to advance a tissue penetrator from within a blood vessel, through the wall of the blood vessel to a target location. The catheter includes at least one stabilizing device thereon for stabilizing catheter prior to advancing the tissue penetrator. The tissue penetrator may extend through a lumen in the body of the catheter and project transversely through an exit port. The stabilizing device may be located closely adjacent to the exit port, or may surround the exit port. The stabilizing device may be one or more balloons, or other mechanical structure that is expandable into contact with the inner luminal wall of the blood vessel. Desirably, the exit port is forced into contact with the blood vessel wall to shorten the distance that the tissue penetrator projects from the catheter body to the target location. The catheter is particular useful for forming blood flow tracts between blood vessels, in particular in coronary revascularization procedures.

Abstract: A catheter having one or more radio-opaque bands near the distal end is designed to be inserted into the renal artery so that the distal end of the catheter is adjacent to the origin of the renal artery. An X-ray image of the bands is used to position the X-ray head relative to the aorta and renal artery so that a useful, unobstructed radiological image perpendicular to the axis of the renal artery at its origin is obtained. This facilitates the positioning of a stent in the renal artery so that the stent encompasses the origin and extends no more than about three millimeters into the aorta. Two radio-opaque bands placed close to one another define a narrow radio-translucent band such that when the X-ray head is rotated to a position where parallax is reduced and the radio-translucent band can be imaged, the renal artery can be appropriately imaged without being obscured by the aorta.