Intracorporeal device with radiopaque marker

Claim 2

An intracorporeal device comprising: a) an elongated shaft having a proximal end and a shaped distal end defining a deflection plane; and b) an asymmetric radiopaque marker member disposed on the elongated shaft proximal to the shaped distal end thereof, the radiopaque marker having a first radiopaque section spaced longitudinally or transversely from a second radiopaque section and an asymmetrical plane which passes through a longitudinal axis of the elongated shaft and which is parallel to the deflection plane so as to allow an operator to fluoroscopically detect the orientation of the distal end of the elongated shaft within a patient.

Claim 3

The intracorporeal device of claim 1 wherein the radiopaque marker member is disposed within the elongated shaft.

Claim 4

The intracorporeal device of claim 1 wherein the radiopaque marker member is comprised of a radiopaque metal.

Claim 5

The intracorporeal device of claim 1 wherein the radiopaque marker member is comprised of a polymeric material loaded with a radiopaque material.

Claim 6

The intracorporeal device of claim 1 wherein the radiopaque marker member is formed by a boundary between a first cylindrical shaft portion and an adjacent second cylindrical shaft portion, wherein the first shaft portion has a different radiopacity than the second shaft portion.

Claim 7

The intracorporeal device of claim 1 wherein the radiopaque marker member is affixed to the inside wall surface of the shaft.

Claim 8

The intracorporeal device of claim 1 wherein the radiopaque marker member is an asymmetric joint connecting a first and second portion of the shaft.

Claim 9

An intracorporeal device comprising: a) an elongated shaft having a proximal end and a shaped distal end; and b) a radiopaque marker member disposed upon the elongated shaft proximal to the shaped distal end and having a shape conforming generally to the shape of the shaft, the marker member having a first longitudinal section that does not completely surround a circumference of the shaft, and a second longitudinal section that does completely surround the circumference of the shaft so as to create a radioscopic projection which reveals the orientation of the distal end of the elongated shaft.

Claim 10

An intracorporeal device comprising: a) an elongated shaft having a proximal end and a shaped distal end; and b) a radiopaque marker member disposed upon the elongated shaft proximal to the shaped distal end and having a shape conforming generally to the shape of the shaft, the marker member having a first longitudinal section that does not completely surround a circumference of the shaft, and a second longitudinal section that does completely surround the circumference of the shaft so as to create a radioscopic projection which reveals the orientation of the distal end of the elongated shaft.

Claim 11

The intracorporeal device of claim 8 wherein the radiopaque marker member is disposed within the elongated shaft.

Claim 12

The intracorporeal device of claim 8 wherein the radiopaque marker member is comprised of a radiopaque metal.

Claim 13

The intracorporeal device of claim 8 wherein the radiopaque marker member is comprised of a polymeric material loaded with a radiopaque material.

Claim 14

The intracorporeal device of claim 8 wherein the radiopaque marker member is formed by a boundary between a first shaft portion and a second shaft portion wherein the first shaft portion has a different radiopacity than the second shaft portion.

Claim 15

The intracorporeal device of claim 8 wherein the radiopaque marker member is affixed to the inside wall surface of the shaft.

Claim 16

The intracorporeal device of claim 8 wherein the radiopaque marker member is an asymmetric joint connecting a first and second portion of the shaft.

Claim 17

A delivery catheter system for the delivery of an elongated therapeutic or diagnostic device to perform a procedure in a region of a patient's heart wall which defines at least in part a left ventricle of the patient's heart, comprising: a) a first delivery catheter which has proximal and distal ends, a port in the distal end, an inner lumen extending therein to and in fluid communication with the port in the distal end, a relatively straight main shaft section and a shaped distal shaft section having at least one segment forming an angle with respect to a proximally adjacent portion of the main shaft section so that the shaped distal shaft section has a discharge axis which can generally be aligned with or parallel to a longitudinal axis of the patient's left ventricle; and b) a second elongated delivery catheter which is slidably and rotatably disposed within the inner lumen of the first delivery catheter, which is longer than the first delivery catheter and which has a proximal end and a shaped distal end, a port in the distal end, an inner lumen extending to and in fluid communication with the port in the distal end configured to slidably receive an elongated ablation device, an elongated main shaft section at least a portion of which is aligned with the discharge axis of the first delivery catheter and a distal section configured to have a discharge axis at an angle of about 80° to about 135° with respect to a portion of the main shaft section thereof aligned with the discharge axis of the first delivery catheter so as to be normal to the region of the heart wall to be subjected to the procedure; and c) a radiopaque marker member disposed on the elongated shaft of the second delivery catheter proximal to the shaped distal end thereof and which has a first radiopaque section spaced longitudinally or transversely from a second radiopaque section so as to allow an operator to fluoroscopically detect the orientation of the distal end of the elongated shaft within a patient.

Claim 18

A delivery catheter system for the delivery of an elongated therapeutic or diagnostic device to perform a procedure in a region of a patient's heart wall which defines at least in part a left ventricle of the patient's heart, comprising: a) a first delivery catheter which has proximal and distal ends, a port in the distal end, an inner lumen extending therein to and in fluid communication with the port in the distal end, a relatively straight main shaft section and a shaped distal shaft section having at least one segment forming an angle with respect to a proximally adjacent portion of the main shaft section so that the shaped distal shaft section has a discharge axis which can generally be aligned with or parallel to a longitudinal axis of the patient's left ventricle; and b) a second elongated delivery catheter which is slidably and rotatably disposed within the inner lumen of the first delivery catheter, which is longer than the first delivery catheter and which has a proximal end and a shaped distal end, a port in the distal end, an inner lumen extending to and in fluid communication with the port in the distal end configured to slidably receive an elongated ablation device, an elongated main shaft section at least a portion of which is aligned with the discharge axis of the first delivery catheter and a distal section configured to have a discharge axis at an angle of about 80° to about 135° with respect to a portion of the main shaft section thereof aligned with the discharge axis of the first delivery catheter so as to be normal to the region of the heart wall to be subjected to the procedure; and c) a radiopaque marker member disposed on the elongated shaft of the second delivery catheter proximal to the shaped distal end thereof and which has a first radiopaque section spaced longitudinally or transversely from a second radiopaque section so as to allow an operator to fluoroscopically detect the orientation of the distal end of the elongated shaft within a patient.

Claim 19

The delivery catheter system of claim 15 wherein the shaped distal shaft section of the second delivery catheter is configured to have a discharge axis at an angle of about 90° to about 120° with respect to the portion of the main shaft section thereof aligned with the discharge axis of the first delivery catheter.

Claim 20

The delivery catheter system of claim 15 wherein the shaped distal section of the first delivery catheter has at least a first segment and a proximally adjacent second segment.

Claim 21

The delivery catheter system of claim 15 wherein the radiopaque marker member is disposed within the elongated shaft.

Claim 22

The delivery catheter system of claim 15 wherein the radiopaque marker member is comprised of a radiopaque metal.

Claim 23

The delivery catheter system of claim 15 wherein the radiopaque marker member is comprised of a polymeric material loaded with a radiopaque material.

Claim 24

The delivery catheter system of claim 15 wherein the radiopaque marker member is formed by a boundary between a first shaft portion and a second shaft portion wherein the first shaft portion has a greater radiopacity than the second shaft portion.

Claim 25

The delivery catheter system of claim 15 wherein the radiopaque marker member is formed by a boundary between a first cylindrical shaft portion and an adjacent second cylindrical shaft portion, wherein the first shaft portion has a greater radiopacity than the second shaft portion.

Claim 26

The delivery catheter system of claim 15 wherein the radiopaque marker member is affixed to the inside wall of the elongated shaft.

Claim 27

The delivery catheter system of claim 15 further comprising a second radiopaque marker member disposed on the straight main shaft spaced proximally to the distal end thereof.

Claim 28

A delivery catheter system for the delivery of an elongated device to perform a therapeutic or diagnostic procedure in a region of a patient's heart wall which defines at least in part a left ventricle of the patient's heart, comprising a) a first delivery catheter which has proximal and distal ends, a port in the distal end, an inner lumen extending therein to and in fluid communication with the port in the distal end, a relatively straight main shaft section and a shaped distal shaft section having at least one segment forming an angle with respect to a proximally adjacent portion of the main shaft section so that the shaped distal shaft section has a discharge axis which can generally be aligned with or parallel to a longitudinal axis of the patient's left ventricle; b) a second elongated delivery catheter which is slidably and rotatably disposed within the inner lumen of the first delivery catheter, which is longer than the first delivery catheter and which has a proximal end and a shaped distal end, a port in the distal end, an inner lumen extending to and in fluid communication with the port in the distal end configured to slidably receive and elongated ablation device, an elongated main shaft section at least a portion of which is aligned with the discharge axis of the first delivery catheter and a distal section configured to have a discharge axis at an angle of about 80° to about 135° with respect to a portion of the main shaft section thereof aligned with the discharge axis of the first delivery catheter so as to be normal to the region of the heart wall to be subjected to the procedure; and c) a radiopaque marker member disposed upon the elongated shaft of the second delivery catheter proximal to the shaped distal end and having a shape which conforms to the shape of the shaft and which has a first longitudinal section that does not completely surround a circumference of the shaft and a second longitudinal section that does completely surround the circumference of the shaft so as to create a radioscopic projection which reveals the orientation of the distal end of the elongated shaft.

Claim 29

A delivery catheter system for the delivery of an elongated device to perform a therapeutic or diagnostic procedure in a region of a patient's heart wall which defines at least in part a left ventricle of the patient's heart, comprising a) a first delivery catheter which has proximal and distal ends, a port in the distal end, an inner lumen extending therein to and in fluid communication with the port in the distal end, a relatively straight main shaft section and a shaped distal shaft section having at least one segment forming an angle with respect to a proximally adjacent portion of the main shaft section so that the shaped distal shaft section has a discharge axis which can generally be aligned with or parallel to a longitudinal axis of the patient's left ventricle; b) a second elongated delivery catheter which is slidably and rotatably disposed within the inner lumen of the first delivery catheter, which is longer than the first delivery catheter and which has a proximal end and a shaped distal end, a port in the distal end, an inner lumen extending to and in fluid communication with the port in the distal end configured to slidably receive and elongated ablation device, an elongated main shaft section at least a portion of which is aligned with the discharge axis of the first delivery catheter and a distal section configured to have a discharge axis at an angle of about 80° to about 135° with respect to a portion of the main shaft section thereof aligned with the discharge axis of the first delivery catheter so as to be normal to the region of the heart wall to be subjected to the procedure; and c) a radiopaque marker member disposed upon the elongated shaft of the second delivery catheter proximal to the shaped distal end and having a shape which conforms to the shape of the shaft and which has a first longitudinal section that does not completely surround a circumference of the shaft and a second longitudinal section that does completely surround the circumference of the shaft so as to create a radioscopic projection which reveals the orientation of the distal end of the elongated shaft.

Claim 30

The delivery catheter system of claim 25 wherein the shaped distal shaft section of the second delivery catheter is configured to have a discharge axis at an angle of about 90° to about 120° with respect to the portion of the main shaft section thereof aligned with the discharge axis of the first delivery catheter.

Claim 31

The delivery catheter system of claim 25 wherein the shaped distal section of the first delivery catheter has at least a first segment and a proximally adjacent second segment.

Claim 32

The delivery catheter system of claim 25 wherein the radiopaque marker member is disposed within the elongated shaft.

Claim 33

The delivery catheter system of claim 25 wherein the radiopaque marker member is comprised of a radiopaque metal.

Claim 34

The delivery catheter system of claim 25 wherein the radiopaque marker member is comprised of a polymeric material loaded with a radiopaque material.

Claim 35

The delivery catheter system of claim 25 wherein the radiopaque marker member is affixed to the inside wall of the elongated shaft.

Claim 36

The delivery catheter system of claim 25 further comprising a second radiopaque marker member disposed on the straight main shaft spaced proximally to the distal end thereof.

Claim 37

A delivery catheter system for the delivery of an elongated device to perform a therapeutic or diagnostic procedure in a region of a patient's heart wall which defines at least in part a left ventricle of the patient's heart, comprising a) a first delivery catheter which has proximal and distal ends, an inner lumen extending therein, a relatively straight main shaft section and a shaped distal shaft section having at least one segment forming an angle with respect to a proximally adjacent portion of the main shaft section so that the shaped distal shaft section has a discharge axis which can generally be aligned with or parallel to a longitudinal axis of the patient's left ventricle; b) a second elongated delivery catheter which is slidably and rotatably disposed within the inner lumen of the first delivery catheter, which is longer than the first delivery catheter and which has a proximal end and a shaped distal end, an inner lumen configured to slidably receive an elongated ablation device, an elongated main shaft section at least a portion of which is aligned with the discharge axis of the first delivery catheter and the shaped distal section configured to have a discharge axis at an angle of about 80 ° to about 135 ° with respect to a portion of the main shaft section thereof aligned with the discharge axis of the first delivery catheter so as to be normal to the region of the heart wall to be subjected to the procedure; and c) a radiopaque marker member disposed within the elongated shaft of the second delivery catheter proximal to the shaped distal end so as to allow an operator to fluoroscopically detect the orientation of the distal end of the delivery catheter system within a patient.

Claim 38

A delivery catheter system for the delivery of an elongated device to perform a therapeutic or diagnostic procedure in a region of a patient's heart wall which defines at least in part a left ventricle of the patient's heart, comprising a) a first delivery catheter which has proximal and distal ends, an inner lumen extending therein, a relatively straight main shaft section and a shaped distal shaft section having at least one segment forming an angle with respect to a proximally adjacent portion of the main shaft section so that the shaped distal shaft section has a discharge axis which can generally be aligned with or parallel to a longitudinal axis of the patient's left ventricle; b) a second elongated delivery catheter which is slidably and rotatably disposed within the inner lumen of the first delivery catheter, which is longer than the first delivery catheter and which has a proximal end and a shaped distal end, an inner lumen configured to slidably receive an elongated ablation device, an elongated main shaft section at least a portion of which is aligned with the discharge axis of the first delivery catheter and the shaped distal section configured to have a discharge axis at an angle of about 80 ° to about 135 ° with respect to a portion of the main shaft section thereof aligned with the discharge axis of the first delivery catheter so as to be normal to the region of the heart wall to be subjected to the procedure; and c) a radiopaque marker member disposed within the elongated shaft of the second delivery catheter proximal to the shaped distal end so as to allow an operator to fluoroscopically detect the orientation of the distal end of the delivery catheter system within a patient.