US20120006479A1 - Rapid Exchange Balloon Catheter and Method for Making Same - Google Patents

Rapid Exchange Balloon Catheter and Method for Making Same Download PDF

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US20120006479A1
US20120006479A1 US13/240,129 US201113240129A US2012006479A1 US 20120006479 A1 US20120006479 A1 US 20120006479A1 US 201113240129 A US201113240129 A US 201113240129A US 2012006479 A1 US2012006479 A1 US 2012006479A1
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transitional region
distal end
bending stiffness
processing step
metal body
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US13/240,129
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Palle M. Hansen
Steen Aggerholm
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Cook Medical Technologies LLC
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Cook Medical Technologies LLC
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/10Balloon catheters
    • A61M25/1027Making of balloon catheters
    • A61M25/1036Making parts for balloon catheter systems, e.g. shafts or distal ends
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/0043Catheters; Hollow probes characterised by structural features
    • A61M25/0054Catheters; Hollow probes characterised by structural features with regions for increasing flexibility
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M25/00Catheters; Hollow probes
    • A61M25/01Introducing, guiding, advancing, emplacing or holding catheters
    • A61M2025/0183Rapid exchange or monorail catheters
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T156/00Adhesive bonding and miscellaneous chemical manufacture
    • Y10T156/10Methods of surface bonding and/or assembly therefor

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Pulmonology (AREA)
  • Biophysics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Media Introduction/Drainage Providing Device (AREA)
  • Materials For Medical Uses (AREA)

Abstract

A rapid exchange balloon catheter having a proximal end and a distal end, the catheter including a tubular metal shaft body extending from the proximal end along a majority of the total length and having an inflation lumen arranged therein, a plastics distal end portion bonded to the metal body in extension thereof, the distal end portion being provided with an inflation lumen in communication with a balloon, and a guide wire lumen, the guide wire lumen extending from a proximal side port to a distal end opening. To reduce the resistance to kinking, the metal body includes a transitional region having reduced stiffness at the position of bonding to the plastics distal end portion compared to a more proximal position along the metal body.

Description

    RELATED APPLICATIONS
  • This application is a division of U.S. application Ser. No. 12/093,034, which has a filing date under 35 U.S.C. §371(c) of Sep. 11, 2008, which claims the benefit under 35 U.S.C. §371 of International Application No. PCT/US2006/044495, filed Nov. 16, 2006, which claims the benefit of U.S. Provisional Application Ser. No. 60/737,124, filed Nov. 16, 2005. These references are incorporated herein in their entirety.
  • FIELD OF THE INVENTION
  • The present invention relates to a rapid exchange balloon catheter.
  • BACKGROUND OF THE INVENTION
  • Catheters have found widespread use in medical procedures, such as percutaneous transluminal coronary angioplasty (PTCA) or for delivery of stents. Most catheters are guided to the application site by sliding the catheter along a guide wire, which has been carefully advanced and arranged within the patient. During advancement of the catheter along the guide wire, it is important to keep the guide wire steady. Ordinary catheters are guided to the application site in a patient by sliding the catheter along a guide wire extending all the way through a lumen of the catheter from the proximal end to the distal end thereof. To enable the physician to hold or manipulate the guide wire during advancement of the catheter along the guide wire, it is necessary to have an excess length of guide wire. The guide wire must hence have a length of about twice the length of the catheter, e.g. 3 m in total, which greatly impedes the procedure. An important sub-category of catheters are catheters of the well-known so-called rapid exchange type, which greatly facilitate operation, especially exchange of catheters if it is found during a procedure that a different kind or size of catheter is needed for the specific purpose. In the rapid exchange catheter, the guide wire only passes through a minor part of the catheter at the distal end thereof, whereas along a majority of the catheter, the guide wire runs in parallel with the catheter. Hence it is not necessary to have an excess length of guide wire. However the rapid exchange catheter provides some challenges, especially with regard to resistance to kinking of the catheter.
  • An important feature of catheters is the transmission of force, the so-called push force, from the proximal end to the distal end of the catheter. This transmission significantly affects the physician's ability to direct the distal end of the catheter into a body lumen of a patient by manipulating the proximal end thereof. Another important feature of catheters is the flexibility of the distal end to bend and conform to the body lumen wall without causing any injury to the lumen wall. Hence catheters, especially of the rapid exchange type, are commonly manufactured of a metal proximal shaft portion of relatively stiffness, and a relatively flexible plastics distal portion bonded to the metal shaft portion. An abrupt change of properties between the shaft portion and the distal portion however increases the risk of twist and kinking. Hence there is a need to provide a good transition between the relatively stiff proximal section to the relatively more flexible distal section to provide a sufficient resistance to twist and kinking while maintaining flexibility and ability to bend.
  • U.S. Pat. No. 6,746,423 discloses a catheter with a reinforcing member at a rapid exchange junction. Although this construction has some effect on the kink resistance, it is somewhat difficult to manufacture and hence expensive. This is due to the fact that the construction introduces a separate element, namely a reinforcing member, which must be securely bonded to the catheter. The reinforcing member must be stocked and handled inevitably raising the cost, and further there is an increased risk of leakage from the catheter due to the extra joints, thereby raising the costs to skilled personnel and quality check.
  • It is hence an object of the invention to provide an alternative catheter with reduced risk of kinking.
  • SUMMARY OF THE INVENTION
  • The present invention relates to a rapid exchange balloon catheter having a proximal end and a distal end, said catheter comprising: a tubular metal shaft body extending from the proximal end along a majority of the total length and having an inflation lumen arranged therein, a plastics distal end portion bonded to the metal body in extension thereof, said distal end portion being provided with an inflation lumen in communication with a balloon, and a guide wire lumen, said guide wire lumen extending from a proximal side port to a distal end opening.
  • The metal body comprises a transitional region having reduced stiffness at the position of bonding to the plastics distal end portion compared to a more proximal position along the metal body. By providing a reduced stiffness transitional region in the metal body, there is avoided an abrupt junction from the relatively stiff metal body to the relatively flexible plastics distal end portion. Through the provision of an integral transitional region with reduced stiffness in the metal body, a separate reinforcing member is obviated, and the disadvantages associated therewith avoided.
  • According to an embodiment the stiffness is defined as bending stiffness, where said bending stiffness of the metal body at a proximal position is at least twice as high as the bending stiffness of the metal body at the distal end of the transitional region. Some effect may be provided with a transitional region having a bending stiffness which does not meet this requirement, but the effect is found to be less than optimum.
  • The effect is more pronounced when the bending stiffness of the metal body at a proximal position is at least four times, preferably at least eight times as high as the bending stiffness of the metal body at the distal end of the transitional region.
  • A catheter having very favourable properties in relation to kink resistance may be provided by a catheter wherein the bending stiffness of the metal body at a proximal position is at least twenty times as high as the bending stiffness of the metal body at the distal end of the transitional region. Hereby a very smooth transition between the relatively stiff metal body and the relatively flexible plastics portion is provided, and hence the risk of kinking is very low.
  • The catheter may be made from any suitable metal material, such as stainless steel, which is a well-known and relatively low cost material. According to an embodiment, however, the metal body is at least partly made of a shape memory nickel-titanium alloy. Such nickel-titanium (Nitinol) alloys are superelastic and are found to provide catheters having increased pushability and torquability in the narrow bends and curvature of the vascular system of a patient.
  • According to an embodiment the transitional region has a length of 1 to 50 mm, preferably at least 5 mm and less than 25 mm, and preferably about 10 mm. As is evident to the skilled person, the chosen length of the transitional region is a compromise between contradictory requirements. A length of less than 1 mm would normally not be sufficient to provide a satisfactory transitional region as such a short length will entail a relatively abrupt change of properties. Length in excess of 50 mm would normally not have any positive effect on the kink resistance, and may increase the cost of the catheter. A length of about 10 mm is found to provide a favourable compromise, but lengths of between 5 mm and 25 mm is expected to provide good results, depending on the size of the catheter and the materials used.
  • The reduced stiffness of the transitional region may be accomplished in any suitable way, and according to an embodiment the transitional region comprises weakenings, such as cut-outs, reduced wall thickness or the like. Such machining is relatively cheap and can be performed with e.g. laser cutting. A gradual transition can be achieved by careful choice of size and spacing of the weakenings.
  • According to an alternative or supplementary embodiment the transitional region has been subject to heat treatment at temperatures of 300-600° C. for a period of 10 s to 24 h, whereby the physical properties of the nitinol alloy is permanently altered, and inter alia the stiffness is reduced. Different alloys may respond differently to heat treatment, and the choice of temperature and processing period is a compromise between speed of manufacture, cost of the process and the effect achieved. The skilled person would recognise that the process period should be chosen as short as possible, but a period of less than 10 s will normally not be enough to change the physical properties of the alloy, even for diminutive objects, such as the end of a small diameter catheter. On the other hand processing periods of more than 24 hours increases the processing cost significantly, and should be avoided, and further longer processing times will normally not have any substantial effect on the physical properties of relatively small objects like catheters.
  • Another aspect of the invention relates to a method for manufacturing a rapid exchange balloon catheter comprising the steps of: providing a tubular metal shaft body with an inflation lumen arranged therein, providing a plastics distal end portion, said distal end portion being provided with an inflation lumen in communication with a balloon, and a guide wire lumen, said guide wire lumen extending from a side port to a distal end opening, subjecting an end of the tubular metal shaft body to a processing step adapted to locally reduce the stiffness of an end region of the tubular metal shaft body to provide a transitional region, and bonding the plastics distal end portion onto said transitional region. Hereby a relatively low cost and consistent method for making a rapid exchange catheter is provided, whereby a high quality catheter with improved kink resistance can be manufactured.
  • According to an embodiment, the tubular metal shaft body is made of a superelastic alloy, and wherein the processing step involves heat treating the transitional region at temperatures of 300-600° C. for a period of 10 s to 24 h. The heat treatment may be accomplished by dipping the transitional region into a heated salt bath.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • In the following the invention will be described in more detail, by way of example only, and with reference to the drawing, in which
  • FIG. 1 is a side view, partly in section, of a prior art catheter,
  • FIG. 2 is a side view of a catheter according to the invention, and
  • FIG. 3 is an enlarged schematic view of FIG. 2 of a shaft portion with transitional region.
  • DETAILED DESCRIPTION
  • A prior art rapid exchange catheter according to U.S. Pat. No. 6,746,423 as discussed above is seen in FIG. 1. This prior art catheter 1′ comprises a tubular metal shaft body 2′ extending from the proximal end along a majority of the total length and having an inflation lumen 3′ arranged therein. The catheter 1′ further comprises a plastics distal end portion 41 bonded to the metal body in extension thereof. The distal end portion 4′ is provided with an inflation lumen 5′ and a guide wire lumen 6′, said guide wire lumen 6′ extending from a proximal side port 7′ to a distal end opening 8′. The catheter 1′ further comprises a balloon 9′ arranged at the distal end of the catheter. This prior art catheter 1′ further incorporates a reinforcing member 10′ in form of a tube bridging the region of junction between the metal body 2′ and the plastics distal end portion 4′.
  • In FIG. 2 is shown a catheter according to the invention. This figure is somewhat distorted for illustration purposes, as the total length of the catheter is about 140 cm. The catheter 11 has a proximal end 12 and a distal end 13. The catheter 11 comprises tubular metal shaft body 14 made of a nitinol alloy. An inflation lumen 15 is extending in the full length of the metal shaft body 14. A plastics distal end portion 16 is attached to the end of the tubular metal shaft body 14 by bonding. The plastics distal end portion 16 comprises a side port 17 for a guide wire (not shown) at a proximal side of an inflatable balloon 18, so the guide wire may extend through the most distal part of the catheter to the distal end opening 19.
  • FIG. 3 is a schematic illustration of a part of the tubular metal shaft body 14 of the catheter in FIG. 2. As illustrated the tubular metal shaft body 14 comprises a main region 14 a and a transitional region 14 b, and the main region 14 a and the transitional region 14 b are integral. However the bending stiffness of the transitional region 14 b is substantially lower than the bending stiffness of the main region 14 a. In the embodiment the tubular metal shaft body 14 is made of a nitinol alloy. The bending stiffness may be defined as the resistance to bending when a beam is subjected to a load in transverse direction. As an example one tubular metal shaft body having high bending stiffness may deflect by e.g. 5 mm when a 20 N force is applied at the end of the shaft body in a direction at right angles to the longitudinal direction of the shaft, whereas a similar tubular metal shaft body relatively having low bending stiffness may deflect 20 mm in response to the same load.
  • A prototype of the catheter according to the invention used Nitinol SE508 tubing available from NDC (Nitinol Devices & Components). The composition of this particular nickel-titanium alloy (in weight percent) is as follows: Nickel (nominal): 55.8%, Titanium: balance, Oxygen (max): 0.05%, Carbon (max): 0.02%. The properties of nitinol alloys are dependent on processing history and ambient temperature, and for example Modulus of Elasticity of this alloy is given as an interval of 41-75×103 MPa. The delivered tubes had an outer diameter of 0.25 mm and an inner diameter of approx 0.20 mm. The tubes delivered from NDC had an overall transition temperature below 18° C. The tubes were cut to have a length of 10.00 cm and divided in first part (5.0 cm) and a second part (5.0 cm).
  • Nickel-titanium alloys, such as nitinol, are known to possess special properties, e.g. shape memory and superelastic properties. Nitinol is capable of reversible thermoelastic transformation due to phase transition.
  • The second part was subjected to the following thermal treatment (performed by ADMEDES Schuessler, Germany): the second part was placed in a salt bath heated to 540-550° C. for approximately 20 hours, while the first part was kept cool as close to room temperature as possible. After the thermal treatment, the second part of the nitinol tubes had a transition temperature in the range of about 28-32° C. Thus, above 32° C. the second part of the tubes was in an austenitic phase with a relatively high bending stiffness. Below 28° C. the second part of the tubes was in a Martensitic phase with a significantly lower bending stiffness. The first part of the tubes maintained a transition temperature below 18° C. and appeared rather stiff.
  • Shorter or longer periods may be used as may higher or lower temperatures, depending on the material being heat treated and the desired properties of the material. With the above material, the range of parameters should be approximately 520-600° C. and 30 minutes to 24 hours.
  • By locally heat treating regions of the metal body, it is possible to produce a metal body with spatial variations in physical properties, such as elasticity and stiffness of the metal body. Depending on the extent of the heat treatment, the metal material may simply have a reduced stiffness in the locally treated region or the superelasticity of the locally treated portion may be destroyed, so this region is plastically deformable.
  • By the local heat treatment of the superelastic alloy, the Modulus of Elasticity (i.e. the stress-strain behaviour of the material or stiffness) of different regions can be different due to different phases of the alloy, e.g. Austenitic phase or Martensitic phase. Hence in one region the alloy may exhibit superelastic properties (highly flexible), whereas in another region the alloy may exhibit plastic properties. The Modulus of Elasticity (or stiffness) of the two regions would be different and hence the stress-strain behaviour would be different.
  • According to an embodiment the tubular metal shaft body 14 made of nitinol is subjected to a localized heat treatment to provide a transitional region 14 b having reduced stiffness. This localized heat treatment may be accomplished by any suitable method, such as dipping into a hot salt bath as mentioned above. Alternative methods include electrical resistance heating, laser heating, using a jet of hot inert gas, or using an induction coil to heat the desired portion to provide a transitional region.
  • Suitable materials for the plastics distal end portion include for example various synthetic polymer materials, polyimid, polyamid etc., and other materials as will be evident to the skilled person.
  • The inner diameter of the proximal end of the plastics distal end portion could be chosen to be slightly larger than the outer diameter of the tubular metal body shaft distal end, so the plastics distal end portion can be slid onto the tubular metal body shaft and bonded thereto. Bonding may be accomplished by a suitable type of glue or by thermal bonding of the plastics distal end portion to the metal body, such as by using a laser.

Claims (18)

1. A method for manufacturing a rapid exchange balloon catheter comprising the steps of:
providing a tubular metal shaft body with an inflation lumen arranged therein;
providing a plastics distal end portion, the distal end portion being provided with an inflation lumen in communication with a balloon, and a guide wire lumen, the guide wire lumen extending from a side port to a distal end opening;
subjecting an end of the tubular metal shaft body to a processing step adapted to locally reduce the stiffness of an end region of the tubular metal shaft body to provide a transitional region; and
bonding the plastics distal end portion onto the transitional region.
2. The method according to claim 1, wherein prior to the processing step any one or any combination of the composition, shape and dimension of the tubular metal shaft body is substantially unchanging along its length.
3. The method according to claim 1, wherein the tubular metal shaft body is made of a superelastic alloy, and wherein the processing step involves heat treating the transitional region at temperatures of 300-600° C. for a period of 10 seconds to 24 hours.
4. The method according to claim 1, wherein the processing step comprises heat treating the transitional region at temperatures of about 540-550° C. for about 20 hours.
5. The method according to claim 1, wherein the processing step comprises heat treating the transitional region at temperatures of about 520-600° C. for about 30 minutes to 24 hours.
6. The method according to claim 1, comprising maintaining a region of the tubular metal shaft body other than the transitional region at about room temperature during the processing step.
7. The method according to claim 1, wherein the processing step comprises heat treatment comprising dipping the transitional region into a heated salt bath.
8. The method according to claim 1, wherein the processing step comprises heat treatment comprising electrical resistance heating, laser heating, using a jet of hot inert gas, using an induction coil or combinations thereof.
9. The method according to claim 1, comprising providing the plastics portion having an inner diameter that is larger than an outer diameter of the tubular metal body and sliding the plastics portion onto the tubular metal portion before bonding thereto.
10. The method according to claim 1, wherein bonding the plastics distal end portion onto the transitional region comprises gluing.
11. The method according to claim 1, wherein bonding the plastics distal end portion onto the transitional region comprises thermal bonding.
12. The method according to claim 1, wherein the processing step provides the transitional region having a bending stiffness, wherein a bending stiffness of the metal body at a proximal position is at least twice as high as a bending stiffness of the metal body at the distal end of the transitional region.
13. The method according to claim 1, wherein the processing step provides the transitional region having a bending stiffness, wherein a bending stiffness of the metal body at a proximal position is at least four times as high as a bending stiffness of the metal body at the distal end of the transitional region.
14. The method according to claim 1, wherein the processing step provides the transitional region having a bending stiffness, wherein a bending stiffness of the metal body at a proximal position is at least eight times as high as a bending stiffness of the metal body at the distal end of the transitional region.
15. The method according to claim 1, wherein the processing step provides the transitional region having a bending stiffness, wherein a bending stiffness of the metal body at a proximal position is at least twenty times as high as a bending stiffness of the metal body at the distal end of the transitional region.
16. The method according to claim 1, further comprising providing weakenings in the transitional region.
17. The method according to claim 1, further comprising providing cutouts in the transitional region.
18. The method according to claim 1, further comprising providing a reduced wall thickness in the transitional region.
US13/240,129 2005-11-16 2011-09-22 Rapid Exchange Balloon Catheter and Method for Making Same Abandoned US20120006479A1 (en)

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US13/240,129 US20120006479A1 (en) 2005-11-16 2011-09-22 Rapid Exchange Balloon Catheter and Method for Making Same

Applications Claiming Priority (4)

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US73712405P 2005-11-16 2005-11-16
PCT/US2006/044495 WO2007059281A1 (en) 2005-11-16 2006-11-16 Rapid exchange balloon catheter and method for making same
US9303408A 2008-09-11 2008-09-11
US13/240,129 US20120006479A1 (en) 2005-11-16 2011-09-22 Rapid Exchange Balloon Catheter and Method for Making Same

Related Parent Applications (2)

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PCT/US2006/044495 Division WO2007059281A1 (en) 2005-11-16 2006-11-16 Rapid exchange balloon catheter and method for making same
US9303408A Division 2005-11-16 2008-09-11

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US20120006479A1 true US20120006479A1 (en) 2012-01-12

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US13/240,129 Abandoned US20120006479A1 (en) 2005-11-16 2011-09-22 Rapid Exchange Balloon Catheter and Method for Making Same

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AT (1) ATE444093T1 (en)
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US20110160834A1 (en) * 2009-07-02 2011-06-30 William Cook Europe Aps Rapid exchange catheter

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WO2007059281A1 (en) * 2005-11-16 2007-05-24 William Cook Europe Aps Rapid exchange balloon catheter and method for making same
WO2014093465A1 (en) * 2012-12-13 2014-06-19 Volcano Corporation Rotational sensing catheter with self-supporting drive shaft section
WO2014133708A1 (en) 2013-02-26 2014-09-04 Cook Medical Technologies Llc Balloon catheter
US20210298760A1 (en) 2018-08-17 2021-09-30 Empress Medical, Inc. Devices and methods for compressing tumors
US11419610B2 (en) * 2018-08-17 2022-08-23 Empress Medical, Inc. Device and method for passing tension member around tissue mass
US20220346828A1 (en) 2019-09-12 2022-11-03 Free Flow Medical, Inc. Devices, methods, and systems to treat chronic bronchitis

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US5697906A (en) * 1995-11-13 1997-12-16 Boston Scientific Corporation Intra-aortic balloon catheter
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US20040006360A1 (en) * 2002-07-03 2004-01-08 Garakani Morteza Hemmati Balloon catheter
US7527606B2 (en) * 2004-05-27 2009-05-05 Abbott Laboratories Catheter having main body portion with coil-defined guidewire passage
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US10245410B2 (en) * 2009-07-02 2019-04-02 Cook Medical Technologies Llc Rapid exchange catheter

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DE602006009545D1 (en) 2009-11-12
EP1948281B1 (en) 2009-09-30
US20090149808A1 (en) 2009-06-11
WO2007059281A1 (en) 2007-05-24
ATE444093T1 (en) 2009-10-15
US8043256B2 (en) 2011-10-25

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