U.S. patent number 3,682,173 [Application Number 05/081,458] was granted by the patent office on 1972-08-08 for separable catheter insertion device.
This patent grant is currently assigned to Vicra Sterile, Inc.. Invention is credited to John L. Center.
United States Patent |
3,682,173 |
Center |
August 8, 1972 |
**Please see images for:
( Certificate of Correction ) ** |
SEPARABLE CATHETER INSERTION DEVICE
Abstract
A disposable catheter insertion device has a longitudinal slot
running the length of the needle and of the hub member secured to
the needle. The slot facilitates removal of the catheter from the
needle after insertion of the catheter into a patient. A clip
member slidably coacts with the hub member and a coupling sleeve to
prevent longitudinal movement of the catheter during insertion into
a patient.
Inventors: |
Center; John L. (Dallas,
TX) |
Assignee: |
Vicra Sterile, Inc. (Dallas,
TX)
|
Family
ID: |
22164295 |
Appl.
No.: |
05/081,458 |
Filed: |
October 16, 1970 |
Current U.S.
Class: |
604/159;
604/160 |
Current CPC
Class: |
A61M
25/0111 (20130101) |
Current International
Class: |
A61M
25/01 (20060101); A61m 005/00 () |
Field of
Search: |
;128/214.4,221,348,35R,DIG.16 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
Primary Examiner: Truluck; Dalton L.
Claims
What is claimed is:
1. A subcutaneous catheter insertion device comprising:
a needle having a longitudinal bore therethrough, one end of said
needle adapted to facilitate puncture and insertion into
subcutaneous tissue, said needle having a longitudinal slot
extending the length thereof;
a hub member secured to the distal end of the needle having a
longitudinal slot therein aligned with said needle slot;
a walled casing having a hollow interior extending rearwardly of
said hub, and an aperture means through said casing walls;
catheter bearing plate means positioned within said casing opposite
said aperture means;
a flexible catheter having one end slidably disposed in said bore
of said needle and extending rearwardly through the hub and the
said hollow interior of said casing over said catheter bearing
plate means and terminating in a distal end rearwardly of said
casing;
releasable catheter holding means having a part carried internally
of said hollow interior of said casing and an actuating means
extending externally therefrom through said aperture means;
said holding means being movable by manipulation of said actuating
means to move the said part carried internally from a normal locked
position in the said hollow interior to an unlocked position in
said hollow interior; and
said catheter located on said catheter-bearing plate means being
frictionally engaged by said part carried internally when in the
normal locked position and being released to permit longitudinal
movement when the said part carried internally is moved into the
unlocked position in said hollow interior.
2. The device of claim 2 wherein said enlargement is provided by an
increased diametrical portion of said casing.
3. A subcutaneous catheter insertion device comprising:
a needle having a longitudinal bore therethrough, one end of said
needle adapted to facilitate puncture of and insertion into
subcutaneous tissue, said needle having a longitudinal slot
extending the length thereof;
a hub member secured to the distal end of the needle having a
longitudinal slot therein aligned with said needle slot;
a walled casing having a hollow interior extending rearwardly of
said hub, said casing having an enlargement only in a portion of
said hollow interior, said casing further having aperture means
through said casing walls;
catheter bearing plate means positioned within said casing opposite
said aperture means;
a flexible catheter having one end slidably disposed in said bore
of said needle and extending rearwardly through the hub and the
said hollow interior of said casing and over said catheter bearing
plate means and terminating in a distal end rearwardly from said
casing;
releasable catheter holding means having a part carried internally
of said hollow interior of said casing and a part extending
externally therefrom through said aperture means;
said holding means being movable by manipulation of said part
extending externally to move the said part carried internally from
a normal position in the said hollow interior to the enlargement in
said hollow interior;
said catheter located on said catheter bearing plate means being
frictionally engaged by said part carried internally when in the
normal position and being released to permit longitudinal movement
thereof when the said part carried internally is moved into the
enlargement in said hollow interior.
4. The device of claim 2 wherein said casing is a coupling
removably engaged with said hub member.
5. The device of claim 4 further comprising an integral rearward
projection from said hub member.
6. The device of claim 5 wherein said enlargement is provided by an
increased diametrical portion of said casing; and
the said normal position is rearward of said enlargement in said
hollow interior.
7. The device of claim 6 further comprising a pliable elongated sac
attached to said coupling member and surrounding and fully
enclosing the said distal end.
8. A subcutaneous catheter insertion device comprising:
a needle having a longitudinal bore therethrough, one end of said
needle adapted to facilitate puncture of and insertion into
subcutaneous tissue, said needle having a longitudinal slot
extending the length thereof;
a hub member secured to the distal end of the needle having a
longitudinal slot therein, said hub member having a projection
extending rearwardly therefrom with a longitudinal slot in register
with the slot in said hub member;
a flexible catheter having one end slidably disposed in said bore
of said needle and extending rearwardly therefrom through the said
longitudinal slot in said hub and the said longitudinal slot in
said projection;
a walled casing having a hollow interior, said casing overlying
said projection with said hollow interior in communication with
said slot in said projection;
said casing having an enlarged diametrical portion and aperture
means through said walls;
a frictional lug riding in the hollow interior of said casing just
over the slot in said projection, said lug having a finger button
extending externally from said casing through said aperture;
said lug being movable by manipulation of said finger button from a
position in frictional contact with a catheter disposed in said
longitudinal slot in said projection to a position in the enlarged
diametrical portion of said casing where said lug is out of
frictional engagement of said catheter.
9. The device of claim 8 wherein said casing is a removable
coupling carried over said hub projection into engagement with said
hub member.
10. The device of claim 8 wherein said casing and said hub are
integral, said casing having a channel extending its full length to
permit a catheter to be completely removed from said casing.
11. The device of claim 10 further comprising an enlargement in a
portion only of the said channel to permit the said lug to be
removed from said casing.
12. The device of claim 8 wherein said increased diametrical
portion is provided by enlarged external dimensions of portions of
said walled casing which have a uniform wall thickness.
13. The device of claim 8 wherein said increased diametrical
portion is provided by enlarged internal dimensions of said casing
with the external dimensions of said casing being substantially
uniform.
Description
BACKGROUND OF THE INVENTION
This invention relates to medical devices for subcutaneous
introduction of fluids into a patient, and more specifically to a
catheter and insertion device therefor. These devices are generally
used for intravenous infusion, however, they also can be used for
infusion or withdrawal of fluids into or from other regions of the
body. Hereafter, for purposes of simplicity, the devices will be
referred to in relation to intravenous infusion.
Catheters of the general type disclosed herein are available
commercially and have been disclosed in the prior art. For example,
self-contained catheters and insertion devices therefor are
disclosed in U.S. Pat. Nos. 3,000,380; 3,010,453; 3,017,884, and
3,055,361. This general type of catheter was developed for usage
where administration of fluids to a patient had to be either
continuous or where such administration was intermittent over a
prolonged period.
Prior to the development of the self-contained catheters and
insertion devices, intravenous or other infusion of fluid into a
patient was accomplished by means of a sterile needle. This needle
was utilized to puncture the skin and vein of a patient. The needle
was then taped to the surface of the skin. A conduit coupled to a
source of intravenous fluid, for example, a syringe or gravity
bottle type infusion fluid source, was then connected to the
needle. Generally, this type of device has been unsatisfactory. Due
to the rigidity of the needle and muscle flexure of the patient, it
was necessary to remove the needle when an infusion was finished,
and to reinsert the needle each time a new infusion was to be
given. The repetitive removal and reinsertion of the needle caused
puncture damage and bruising to the area of the patient into which
the needle was being inserted. Therefore, those in the medical
field have come to prefer the flexible catheter infusion method.
The prior art flexible catheters for infusion of fluids into the
veins of patients generally include a hollow needle and a fairly
long flexible hollow cannula, the catheter. One end of the catheter
usually has a coupling means or mechanism thereon, for example of
the luer type, for connection to a source of infusion liquid. The
other end of the catheter is slidably disposed within the bore of
the hollow needle. The hollow needle is then inserted into a vein
of a patient. The catheter is pushed through the hollow portion of
the needle into the vein. The needle is then removed leaving the
catheter protruding from the body of the patient. One of the
advantages of this type of injection apparatus is that the needle,
catheter and coupling means can be completely enclosed in a sterile
package which is unopened until the time it is to be used with a
patient. In addition, the materials utilized can be sufficiently
economic to render such devices disposable after use. Thus, the
chances of contamination or the spreading of infection is
substantially lessened compared to the reusable type injection
devices which must be resterilized after every use.
One of the significant drawbacks of this prior art is that once the
insertion needle is withdrawn from the body of the patient leaving
the catheter, the needle cannot be removed from the catheter. It
has been impossible to remove the needle since the catheter at its
protruding end usually contains a coupling mechanism of larger
diameter than the needle bore, as above explained. Since the needle
cannot be removed, it is continuously present on the catheter
outside the patient's body. In the past, the presence of the needle
has been troublesome due to its bulkiness and to the fact that the
patient's skin can easily be accidentally punctured by the needle
point.
Damage to the catheter from the needle can also result. But more
importantly, a catheter must sometimes be partially withdrawn
during the insertion process resulting in accidental cutting or
severing of the catheter by the needle point within the patient's
body. Not only can the severed end of the catheter thus lodge
within the patient, but also small chips or shavings from the
catheter wall can remain within the patient's body. These results
are, of course, intolerable.
Various means have been proposed for resolving these problems. The
initial method proposed was merely to tape the needle with the
catheter running through it to the patient's arm thereby keeping it
out of the way. However, the danger of damage to the catheter and
to the patient's skin still was present although not in as great a
proportion. Another solution is disclosed in U.S. Pat. No.
3,055,361. In that patent, a sleeve which is slidably inserted
around the needle prior to its insertion into the patient's arm is
disclosed. The sleeve is positioned on the portion of the needle
which remains exterior to the patient's body. After the catheter
has been inserted and the needle withdrawn from the patient, the
sleeve is moved toward the pointed end of the needle to cover it.
Frictional contact between the portion of the sleeve not extending
beyond the pointed end of the needle retains the sleeve on the
needle. Thus, the pointed end of the needle is covered preventing
damage to the patient. This apparatus, however, still has
drawbacks. The possibility of damage to the catheter itself still
exists since it is not protected from the pointed end of the needle
by the sleeve. In addition, the bulky needle is still present and
still must be taped or tied to the patient's arm.
Still another approach to the problem, representing an advance over
the prior attempts, is disclosed in U.S. Pat. No. 3,472,232. This
patent discloses a hollow needle containing a longitudinal slot
running along its entire length. The needle, of course, is pointed
at one end. A pressure member is connected to the other end which
serves as a needle hub. Hinged to the pressure member or needle hub
is a projection which can be moved in and out of a slot in the
pressure member and through the needle slot to contact a catheter
slidably disposed in the needle. After the catheter is inserted
into a patient, the needle can be withdrawn from the patient's body
and separated from the catheter by pulling upwardly on the
projection to remove it from the slot in the pressure member and
pulling the catheter through the slot in the needle and the
pressure member. Although representing an advance over prior
attempts at dealing with the needle after removal from the
patient's body, this concept still retains significant
disadvantages. For example, in order to operate the catheter
insertion device of the aforementioned patent, two hands are
necessary; one to hold the needle and the other to release the
pressure member so that the catheter can be inserted. Usually it is
desirable for a sole operator of such a catheter insertion device
to have one hand free to manipulate or hold a patient's appendage
while holding onto the needle insertion device with the other hand.
In addition, the device disclosed in the above-mentioned patent
makes no provision for maintaining the catheter in a sterile
environment during insertion. This also is important in that the
atmosphere surrounding the patient during insertion of the catheter
may not be sufficiently sterile to prevent the spread of infection
into the puncture wound made by the catheter insertion needle. In
addition, the pressure member of the device disclosed in the
above-mentioned patent must also be held down with one finger of
the hand inserting the catheter insertion needle into a patient in
order to seize the catheter. It is important that the pressure
member seize or contact the catheter to prevent the catheter from
sliding longitudinally backwardly in the needle while it is being
inserted. It is most desirable to maintain the forward end of the
catheter near the pointed tip of the insertion needle while the two
are being initially inserted into a patient's body.
It is, therefore, found desirable to develop a catheter insertion
device in which the needle can be completely separated from the
catheter containing a coupling mechanism at its distal end. In
addition, it is desirable to possess a catheter insertion device
which allows manipulation and insertion of the needle and catheter
into a patient with only one hand of the operator. In addition, it
is desirable to maintain the catheter in the sterile environment
while inserting it or sliding it longitudinally through the needle
into a patient's body, still providing for complete removal of the
needle from the catheter. In addition, it is also desirable to
maintain such a device at a low manufacturing cost while
incorporating the additional features heretofore described. A low
manufacturing cost is desirable since it will allow production of
disposable catheter insertion devices incorporating the needle
removability feature.
SUMMARY OF THE INVENTION
The present invention, therefore, solves the foregoing problems
while incorporating the desirable attributes of a disposable
catheter insertion device. The subcutaneous catheter insertion
device of the present invention comprises a needle having a
longitudinal bore therethrough, one end of said needle adapted to
facilitate puncture of and insertion into subcutaneous tissue, said
needle having a longitudinal slot extending the length thereof, a
hub member secured to the distal end of the needle having a
longitudinal slot therein, a flexible catheter having one end
slidably disposed in the bore of the needle and extending
rearwardly therefrom, a coupling member connected operatively to
the hub member, and means associated with the coupling member and
movable to coact with a portion of the catheter between a first
position and a second position, the means in the first position
preventing longitudinal movement of the catheter in the needle. In
an alternative embodiment of the subcutaneous catheter insertion
device, the means can be removably associated with the hub member
and longitudinally movable between a first and a second position,
the means in the first position preventing longitudinal movement of
the catheter in the needle.
BRIEF DESCRIPTION OF THE DRAWINGS
A better understanding of the present invention will be derived
from reading the ensuing specification in conjunction with the
accompanying drawings, in which:
FIG. 1 is a partially exploded perspective view of the catheter and
insertion device of the present invention;
FIG. 2 is a side perspective view of the present invention showing
it completely assembled and partially enclosed by an internally
sterile plastic bag;
FIG. 3 is a partial longitudinal cross-sectional view of the
catheter and insertion device of the present invention;
FIG. 4 is a full cross-sectional view of the device taken along a
section similar to that of 4--4 of FIG. 3;
FIG. 5 is an enlarged top view of the insertion needle of the
present invention;
FIGS. 6, 7, and 8 are respectively top, front and side views of the
stop button of the present invention;
FIG. 9 is a schematic illustration of the method of insertion of
the catheter of the present invention into a patient's vein;
FIG. 10 is a partial cross-sectional view of the insertion device
and coupling member of the present invention showing the release
position for the stop button;
FIG. 11 is a perspective view of the needle insertion device of the
present invention showing removal of the catheter from the slot
thereof;
FIG. 12 is a schematic view of the catheter after the needle has
been removed therefrom;
FIG. 13 is a top view of an alternate embodiment of the insertion
needle of the present invention;
FIG. 14 is a cross-sectional view of the alternate embodiment of
FIG. 13 taken along section line 14--14.
DESCRIPTION OF PREFERRED EMBODIMENTS
As heretofore explained, the present invention will be described in
relation to an intravenous catheter insertion device. It is to be
understood that other subcutaneous punctures can be effected with
the present invention for insertion of the catheter disclosed
herein into other portions or regions of the body of the patient.
Therefore, the invention is intended to be limited only by the
definition contained within the appended claims.
Referring now to FIG. 1, a view of a partially disassembled
catheter and insertion needle of the present invention is
illustrated. Hollow needle 10, preferably made of a surgical steel,
has one end which is cut at a taper to form a point 12. The other
end of the needle is secured in a hub member 14. Both needle 10 and
hub member 14 contain longitudinal slots (better seen in later
figures). A coupling sleeve 16 is arranged for sliding and
removable attachment to a rearward projection 18 on the hub member
14. A clip member 20 is positioned in a channel formed when the
coupling sleeve 16 is slidably disposed upon the rearward
projection 18. The hub member 14 is also provided with a circular
portion 22 of reduced diameter onto which a needle cover 24 can be
removably fitted. The needle cover protects the needle point 12 as
well as the entire needle 10, and prevents the needle from
puncturing packaging material for the entire device. The needle
cover 24 also prevents the persons handling the catheter from being
accidentally punctured by the needle point 12.
Slidably disposed in the bore of the hollow needle 10 is an
elongated flexible tubular catheter 26. The catheter can be
composed of polyurethane, polytetrafluoroethylene, or other
suitable material. The catheter extends through the hub member 14
and along a trough (better seen in later figures) contained in the
rearward projection 18. It extends through the coupling sleeve 16
and terminates at its distal end in a suitable fitting 28, for
example a luer female fitting. A luer plug 30 is provided for
sealingly closing the open end of the fitting 28. The plug 30 is
provided to prevent egress of body fluids from the catheter when it
is being inserted and also when the catheter is not attached to a
fluid infusion device.
In FIG. 2, the needle cover 24 is shown secured onto the reduced
diameter portion 22 of the hub member 14. In addition, plug 30 is
disposed in the luer fitting 28. The coupling sleeve 16 has sealed
around its distal circumference a flexible, preferably transparent
sac 32 sealed at its distal end 34. One function of the coupling
sleeve 16 is to maintain the sac 32 around the catheter 26, the
luer fitting 28 and plug 30 to provide a sterile environment.
Primarily, the coupling sleeve 16 serves to retain the clip member
20 in contact with the catheter 26, as will be better seen
later.
The hub member 14, including its rearward projection 18, needle
cover 24, coupling sleeve 16, and clip member 20 are preferably
molded from synthetic polymeric materials such as polyethylene,
polytetrafluoroethylene, polyamides, or some other material which
is capable of being molded. The flexible sac 32, manufactured from,
for example polyurethane, polyethylene or polyester film, can be
attached to the coupling sleeve 16 by heat sealing or can be merely
taped about the sleeve member utilizing a thin strip of adhesively
backed tape.
Normally, the interior and exterior of the needle 10, the interior
of cover 24, the catheter 26, luer fitting 28, and plug 30 as well
as the entire interior of the flexible sac 32 are sterilized during
manufacture of the catheter device. Of course, the interior of the
coupling sleeve 16 is also sterilized as well as the interior
portion of the clip member 20. After the catheter device as shown
in FIG. 2 is completely assembled, it is housed in a package (now
shown) in which the sterilization procedure takes place. The
package and contents are usually rendered sterile by the
introduction of a gas, such as ethylene oxide, into the package.
The device can also be easily transported and handled in the
package without danger of contamination prior to use.
Referring now to the cross-sectional views of FIG. 3 and FIG. 4,
the needle 10 has formed therein a longitudinal slot 54. The needle
cover 24 is secured upon the reduced diameter portion 22 of the hub
14. The clip member 20 is slidably disposed in a channel 40 formed
by the rearward projection 18 of the hub member 14 and coupling
sleeve 16. The clip 20 is composed of a bottom portion 42 of
sufficient vertical height so as to intimately contact the upper
interior wall of the coupling sleeve 16 and also to press the
catheter 26 against the upper interior surface of the rearward
projection 18 of the hub member 14. This coaction of the lower
portion 42 of the clip member 20 operates to prevent longitudinal
movement of the catheter 26 as it is introduced into a patient. A
second portion 44 of the clip member 20 extends upwardly through a
longitudinal slot 46 in the coupling sleeve 16. The portion 44 of
the clip 20 terminates above the coupling sleeve 16 in a finger or
thumb grip 48 containing serrations or ridges on the top thereof.
During insertion of the needle and catheter into a patient, the
clip member rides in the position shown in FIG. 3.
FIG. 4 is a full transverse cross-sectional view taken along a line
similar to line 4--4 of FIG. 3, which better illustrates the
operation of the clip 20 in relation to the catheter 26. The
rearward projection 18 of the needle hub 14 contains a trough or
channel 50 generally of semi-circular cross section extending the
full length of the projection 18. The catheter 26 rides therein.
The upper surface of the bottom portion 42 of clip 20 contacts the
upper interior wall of coupling sleeve 16. As it does so, it is
forced down upon the top surface of the catheter 26 so as to deform
the catheter, thus frictionally engaging the catheter between the
bottom surface of the bottom portion 42 of the clip member 20 and
the walls of the channel 50 in the projection 18. The frictional
engagement between the channel 50 and the bottom portion 42
prevents longitudinal movement of the catheter 26 as it is inserted
into a patient.
The construction of the hub member 14 and the rearward projection
18 integrally a part thereof as well as the channel 50 is better
understood by reference to FIG. 5. There the needle is shown
secured in the hub member 14, preferably integrally molded
therewith. The longitudinal slot 52 in the hub member 14 and the
longitudinal slot 54 in the needle 10 are provided so that after
the catheter has been inserted into a patient and the needle
removed leaving the catheter in the patient, the catheter can be
separated from the needle and hub member as shown in conjunction
with FIG. 11.
Optionally, a wire stylet 58 as illustrated in FIG. 3 can be
attached to the luer plug 30. The stylet extends from the plug 30
to ordinarily within a half inch from the end of the catheter as
shown. The stylet lends rigidity to the catheter for easier
insertion into a patient. It should be noted that the interior
opening through the coupling sleeve 16 is of sufficient diametral
size such that the luer fitting 28 and plug 30 can pass through the
sleeve 16 so that the sleeve and sac 32 can be completely removed
from the assembly. In addition, it should be noted that the
upwardly extending walls 60 shown both in FIGS. 3 and 5 are
provided so that the coupling sleeve 16 will have additional
surface area on the rearward projection to contact so that it will
be held sufficiently tight merely by frictional contact. The
distance between the interior sides of the upwardly extending walls
60 must be sufficiently wide to allow free passage of the bottom
portion 42 of the clip member 20 therebetween.
FIGS. 6, 7, and 8 present top, front and side views, respectively,
of the clip member 20. It is seen that the clip member is generally
T-shaped and includes a lower portion 42 which is slidably disposed
in the channel formed by the coupling sleeve and the rearward
projection on the hub member. The middle portion 44 extends
upwardly through the slot 52 in the coupling sleeve and terminates
in the thumb grip 48. Thumb grip 48 has the ridges 56 for
increasing a frictional grip between the thumb and the clip
member.
With respect to operation of the catheter device, refer to FIGS. 9
through 12. The needle cover 24 is first removed. The exterior
sides of the hub member 14 as well as the sides of the coupling
sleeve 16 are then grasped between a thumb and forefinger. The skin
and vein 70 are punctured with the pointed end of the needle.
Thereafter, the thumb is utilized to move the clip member 20
forward to a position as shown in FIG. 10. The catheter 26 is thus
released from the grasp of the lower portion 42 of the clip member
so that is is freely and slidably disposed within the coupling
sleeve, hub member and needle. As can be seen in FIG. 10, the
raised portion 72 at the front end of the coupling sleeve 16
contacts the lower surface of the thumb grip 48 such that the lower
portion 42 of the clip 20 is raised from contact with the catheter.
Thereafter, the catheter is grasped with the opposite hand and
manipulated through the coupling sleeve, hub member and needle into
the patient's vein. After the catheter has been inserted the
desired distance into a patient's vein, the needle is removed from
the patient's body leaving the catheter in place in the vein.
Thereafter, the coupling sleeve 16 is removed from the rearward
projection 18 of the hub member 14. It is also removed completely
over the luer fitting and plug attached to the distal end of the
catheter. The coupling member, sac and clip member 20 then can be
discarded.
Thereafter, the catheter can be separated from the needle and hub
member by pulling the catheter through the slot 54 in the needle 10
and through the slot 52 in the hub member 14 as shown in FIG. 11.
The luer fitting 28 can be attached to an infusion source such as
the intravenous bottle 74 shown in FIG. 12 at any time after the
sac is removed. It is, of course, to be understood that the
catheter is made from a sufficiently flexible material to allow
radial deformation thereof as it is removed through the slot 54.
Such materials include polyurethane and polytetrafluoroethylene as
mentioned above. The slot 54 in the needle is preferably of a
slightly smaller width than the diameter of the catheter 26 so that
it must necessarily be deformed in order to be removed. This size
relationship of the catheter and slot is important since it will
cause the catheter to be retained in the needle at all times until
it is forceably removed. The width of the slot 52 in the hub member
14 is generally of slightly greater width than the catheter 26 so
that removal therefrom can be accomplished with ease.
An alternative embodiment of the present invention is shown in
FIGS. 13 and 14. In this embodiment, the hub member, rearward
projection and coupling sleeve are combined into one assembly,
generally designated 80. Referring to both FIGS. 13 and 14, a
needle 82 is integrally molded into the assembly 80. The needle is
provided with a slot like that of needle 10 referred to above in
conjunction with the preferred embodiment. The assembly 80 contains
a longitudinal slot 83 correspondent with the needle slot along its
entire length. A forward wall 84, a rear wall 86 and the top
portion 88 of the assembly 80 form an interior channel 90 in which
is slidably mounted a clip member 92 similar to that described
above. An opening 94 is provided in the top of the assembly 80
communicating with the slot 83 in assembly 80. The opening 94 is so
sized that the bottom portion of clip member 92 can be removed
therethrough. During insertion of the catheter, the clip member 92
is in a rearward position so that it frictionally engages the
catheter 96 between the bottom portion of the clip member and the
bottom of the channel 90 thus holding the catheter longitudinally
stable during insertion. After the needle and catheter have been
inserted into a patient's body, the clip member 92 is moved forward
in the direction of arrow 98 and removed through opening 94. Thus
the catheter 96 is freed so that it is slidably disposed in the
assembly 80 and needle 82, allowing manipulation of the catheter
into a patient's body. Once the needle has been removed from the
patient leaving the catheter inserted, the catheter can be
separated from the needle and clip member through the needle slot
and the slot 83 in the needle assembly 80.
As one of ordinary skill in the art to which the devices of the
subject invention pertain is aware, many variations and
alternatives of the present device can be provided without
departing from the basic invention. The invention, therefore, is to
be limited only as defined in the appended claims.
* * * * *