Safety syringe abstract
The invention provides a safety syringe, which has a cylinder (11),
a syringe needle (21), a needle holder (31) associated to the cylinder
and adapted to hold the syringe needle, and a plunger (41) associated
to the cylinder (11), wherein the plunger (41) comprises a piston
(42) and serves to inject a filling of the cylinder (11) via the
syringe needle (21), and wherein the plunger (41) can be coupled
with the needle holder (31) arranged in the region of a front hole
(12) of the cylinder (11), to retract the needle holder (31) together
with syringe needle (21) into the cylinder (11) by pulling the plunger
(41) once coupled to the needle holder (31) is retracted into the
cylinder by rotating the plunger (41) and pulling the plunger (41)
aft thereby pulling the needle holder (31) into the cylinder (11).
Then the aft end of the plunger (41) is broken off, and a removable
cap (49) from the aft end of the plunger (41) may be placed over
the opening in the forward end of the cylinder (11).
Safety syringe claims
What is claimed is:
1. A safety syringe for injecting or withdrawing fluids and avoiding
inadvertent needle sticks after use comprising: a thin walled barrel
having an inner surface, a forward end and a forward edge, and an
aft end, the barrel fillable with the fluids; a generally cylindrically
shaped needle holder having an outer surface, a forward end and
an aft end, and a central axis, the needle holder outer surface
slidably engaged with the inner surface of the barrel; a hollow
needle attached to the forward end of the needle holder; the needle
holder having a passageway near the central axis from the forward
end to the aft end of the needle holder, such that the hollow needle
and barrel are in fluid communication; the outer surface of the
needle holder having a plurality of generally L-shaped grooves;
the forward end of the inner surface of the barrel having a plurality
of protrusions sized to be received by the plurality of generally
L-shaped grooves, to releasably secure the needle holder to the
forward end of the barrel; the aft end of the needle holder having
a generally cylindrically shaped cavity having an inner surface
with a plurality of upstanding webs; a plunger having a central
axis and having a forward end and an aft end, the plunger at the
forward end having a piston having an outer surface slidably engaged
with the inner surface of the barrel, the piston having a rod extending
to the aft end of the plunger; the forward end of the plunger further
having an anchor member; the aft end of the needle holder having
a generally circular opening sized to receive the anchor member
and having a latching member sized to retain the anchor member inside
the cavity of the needle holder, the latching member being portions
of the opposing of reduced diameter; and the anchor member having
a plurality of flukes sized to catch acting as stops inside on the
plurality of upstanding webs to enlarge the latching members, the
needle holder cavity as the plunger is rotated about the central
axis; and the upstanding webs located adjacent the latching members;
the forward end of the piston rod having a reduced cross section;
whereby after use of the safety syringe the plunger anchor may be
inserted inside the needle holder cavity and the plunger rotated
about the central axis, and the hollow needle pulled inside the
barrel and the plunger broken off at the reduced cross section.
2. The safety syringe of claim 1 wherein the plurality of L-shaped
slots have widened V-shaped entrances for ease of receiving the
plurality of protrusions in assembling the safety syringe.
3. The safety syringe of claim 1 further comprising an O-ring on
the outer surface of the needle holder for sealing any gap between
the needle holder and the inner surface of the barrel.
4. The safety syringe of claim 1 further comprising at least one
O-ring on the outer surface of the piston for sealing any gap between
the outer surface of the piston and the inner surface of the barrel.
5. The safety syringe of claim 1 wherein the reduced cross section
is a notch in the piston rod.
6. The safety syringe of claim 1 wherein the plurality of protrusions
are at the forward edge of the inner surface of the thin walled
barrel for ease of manufacture.
7. The safety syringe of claim 1 wherein the barrel has a substantially
constant diameter except for the plurality of protrusions.
8. The safety syringe of claim 1 wherein the aft end of the plunger
has a cap to facilitate pushing the plunger forward, and at least
a portion of the cap is removable to cover the forward end of the
barrel upon the needle being retracted into the barrel.
Safety syringe description
BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates generally to hypodermic syringes, and more
particularly to such syringes having retractable needles after use
to prevent hazardous needle sticks.
2. Description of the Related Art
The idea of safety syringes with retractable needles to prevent
needle sticks is well known. Initially such devices were bulky,
expensive to manufacture and did not function well. Over the years
as the art progressed they became easier to make and operate, but
still problems remain which have prevented mass manufacture and
use of safety syringes.
Disposable syringes are typically made by automated, high volume
plastic injection molding processes. Since these devices by design
are disposable after one use, they must be very inexpensive to produce
on a per unit basis. The critical parts of the syringe must be structurally
sound and well made. Given the uses of syringes in administering
drugs, stringent quality standards must be maintained.
Mazur U.S. Pat. No. 5401246 disclosed a retractable syringe with
a needle holder and needle in a frangible connection in the forward
end of a syringe barrel. This syringe includes an additional part,
a clip at the forward end of the barrel, which locks the needle
holder in place and prevents inadvertent release from the forward
end of the barrel. To release the needle holder the user must manually
manipulate the clip near the needle, to unlock the needle holder
and allow its retraction into the barrel. This manipulation near
the needle is believed fraught with danger. As is common, the plunger
may be broken off at a weakened section and reinserted into the
other end of the barrel. This device is also believed unnecessarily
complex.
Gloyer U.S. Pat. No. 5304154 disclosed a retractable syringe
with a needle holder in an articulating connection with a thin walled
barrel. Protrusions in the needle holder and slots in the barrel
together provide a mechanism for retaining and releasing the needle
holder. This patent further discloses a plunger/needle holder single-use
snap connection consisting of a protruding latch in the plunger
and a corresponding cavity in the needle holder. Given the variations
in wall thickness of the barrel section to provide the slots, and
the complicated geometry of the needle holder cavity for the snap
connection, this device is believed difficult and expensive to manufacture,
and subject to quality problems.
SUMMARY OF THE INVENTION
A safety syringe for injecting or withdrawing fluids and avoiding
inadvertent needle sticks after use includes a thin-walled cylinder
or barrel fillable with the fluids, a generally cylindrically-shaped
needle holder that slides inside the barrel, and a hollow needle
attached to the forward end of the needle holder. The needle holder
has a through passageway near its central axis, such that the needle
and barrel are in fluid communication. The outer surface of the
needle holder has a number of L-shaped grooves, and the forward
end of the inner surface of the cylinder has a number of corresponding
protrusions sized to be received by the L-shaped grooves, to releasably
secure the needle holder to the forward end of the barrel.
The aft end of the needle holder has a generally cylindrically-shaped
cavity with a number of upstanding webs or stops. The plunger at
the forward end has a piston slidably engaged with the inner surface
of the barrel, the piston having a rod extending to the aft end
of the plunger. The forward end of the plunger further has an anchor
while the aft end of the needle holder has a corresponding generally
circular opening and latch sized to receive and retain the anchor
inside the cavity of the needle holder upon insertion thereon and
rotation of the plunger. The anchor has a plurality of flukes sized
to catch on the stops or upstanding webs in the needle holder cavity
as the plunger is rotated about its central axis; positioning the
anchor to be engaged by the latch. Preferably, the latch is merely
a portion of the opening of reduced diameter. The forward end of
the piston rod may have a reduced cross section, preferably a notch,
to facilitate breaking off of the plunger.
After use of the safety syringe the plunger anchor may be pushed
inside the needle holder cavity and the plunger rotated about its
central axis. Advantageously, if somehow inadvertently coupled together,
the needle holder and plunger may be decoupled by rotating the plunger
back the other direction and pulling the plunger anchor outside
the needle holder cavity. Instead, going forward with retracting
the needle, the plunger is further rotated and pulled back, moving
the needle and holder inside the barrel. Then the plunger broken
off at its reduced cross section, effectively disabling the safety
syringe from further use. Optionally a removable cap may be taken
from the aft end of the plunger and inserted into the open forward
end of the barrel.
Preferably there is an O ring on the outer surface of the needle
holder for sealing any gap between the needle holder and the inner
surface of the barrel. Preferably there is another O ring on the
outer surface of the piston for sealing any gap between the outer
surface of the piston and the inner surface of the barrel.
Preferably the L-shaped slots have widened V-shaped entrances,
for ease of receiving the protrusions in assembling the safety syringe.
Preferably the protrusions are at the forward edge of the inner
surface of the thin walled barrel, for ease of manufacture. Preferably
the thin-walled barrel is a substantially constant diameter and
thickness except for the plurality of protrusions.
OBJECTS OF THE INVENTION
Given the shortcomings of the prior art, further significant improvements
to safety syringes are desirable.
It is an object of the present invention to provide a safety syringe
that minimizes the possibility of inadvertent needle sticks;
It is an object of the present invention to provide a safety syringe
that prevents reuse of the syringe after one use;
It is an object of the present invention to provide a safety syringe
that is inexpensive to manufacture;
It is an object of the present invention to provide a safety syringe
that is easy to make without quality problems;
It is a further object of the present invention to provide a safety
syringe that is simple to use;
It is a further object of the present invention to provide a safety
syringe with a cap to seal the barrel once the needle is retracted
therein.
It is a further object to provide a safety syringe in which if
the plunger and needle holder are inadvertently coupled together
they may be easily separated.
These and other objects and advantages of the present invention
will be apparent from a review of the following specification and
accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is cross-sectional view of the parts.
FIG. 2 is a squint view of the parts.
FIG. 3 is a lateral view of the cylinder.
FIG. 4 is a lateral view of the syringe needle inserter.
FIG. 5 is a front view of the syringe needle inserter.
FIG. 6 is an A--A line cross-sectional view of the FIG. 5.
FIG. 7 is a B--B line cross-sectional view of the FIG. 5.
FIG. 8 is a front view of the plunger.
FIG. 9 is a cross-sectional view of this device when injection
is completed.
FIG. 10 is a cross-sectional view of the device when plunger meets
the syringe needle fixer upon completion of injection.
FIG. 11 is a cross-sectional view of this device which shows the
breaking of the plunger after pulling the plunger back into the
cylinder in order to keep the syringe needle and the syringe needle
fixer inside the cylinder.
FIG. 12 is a partial longitudinal cross-section of the syringe.
FIG. 13 is an isometric exploded view of a needle inserting device.
FIG. 14 is a view of the plunger.
FIG. 15 is a longitudinal cross-section of the syringe without
needle.
FIG. 16 is a longitudinal cross-section of the syringe without
needle that the plunger is assembled with the needle inserting device.
FIG. 17 is a partial cross-section which shows breaking off the
plunger after injection.
FIG. 18 is a longitudinal cross-section of the syringe covered
with a part, separated from the plunger.
FIG. 19 is a longitudinal view of the needle inserting device.
FIG. 20 is an A--A line cross-section in FIG. 12.
FIG. 21 is another A--A line cross-section in FIG. 12.
FIG. 22 is a B--B line cross-section in FIG. 12.
FIG. 23 is a C--C line cross-section in FIG. 19.
FIG. 24 is an E--E line cross-section in FIG. 19.
FIG. 25 is an F--F line cross-section in FIG. 19.
FIG. 26 is a rear perspective view illustrating a needle, portion
of a cylinder, and a needle holder, holder and a front perspective
view of plunger of a third embodiment all disassembled;
FIG. 27 is a section view illustrating the needle holder and cylinder
and a side view of the plunger of the third embodiment;
FIG. 28 is an orientation view illustrating the needle holder and
the various views taken from and through it;
FIG. 29 is a section view illustrating the needle holder;
FIG. 30 is a rear view illustrating the needle holder;
FIG. 31 is a section view of the plunger and cylinder; and
FIG. 32 is a side view illustrating the plunger engaging the needle
holder.
DESCRIPTION OF THE PREFERRED EMBODIMENT(S)
The detailed description set forth below in connection with the
appended drawings is intended as a description of presently preferred
embodiments of the invention and is not intended to represent the
only forms in which the present invention may be constructed and/or
utilized. The description sets forth the structure and the sequence
of steps for constructing and operating the invention in connection
with the illustrated embodiments. It is to be understood, however,
that the same or equivalent structure and sequences of steps may
be accomplished by different embodiments that are also intended
to be encompassed within the spirit and scope of the invention.
This device is for a safety syringe preventing a third person from
getting damaged by the used syringe needles. It is designed to keep
the syringe needle in custody of syringe cylinder once used so that
a third person may not be pricked by the used needles. The plunger
shall then be broken after use in order to prevent from being used
again.
In order to prevent repeated use of syringe needles by far, it
is the current phenomenon that disposable syringes are predominantly
being used. Such conventional disposable syringes have been technically
designed to prevent to be reused.
The conventional disposable syringes are, however, after being
used, usually or frequently being disposed or not properly dealt
with the needles and thus a third person may be easily pricked.
Such problems of giving damages to a third party have not been solved.
Because the syringe needles always have blood stains, in case medical
workers including doctors and nurses as well as a third party get
pricked by a used syringe needle they are very much concerned of
being infected by the disease of the patients (AIDS, hepatitis,
etc.) and such cases have been reported.
This device is a safety syringe system which prevents disease from
being infected to a third party via used syringe needles by keeping
it inside the syringe cylinder.
According to this device, the used needle does not need to be taken
off from the syringe after use, but, instead, it is pulled into
the cylinder to be fixed and kept in custody inside cylinder. And
by doing this, infections of disease to a third party by getting
pricked can be prevented.
My previous patent application of this nature regarding safety
syringe system have been published on the Utility Model Announcement
Korea Utility Model No. 91-4532 and Open Utility Model Public News
Korea Utility Model No. 96-13409.
This device is to introduce more advanced safety syringe system
which is simpler in structure and more reliable in affect compared
with the above-said previous patent.
Technical Target that this device pursue to accomplish.
My previous safety syringe system published on the Utility Model
Announcement No. 91-4532 and Open Utility Model Public News No.
96-13409 was to have the needleset fixed to the plunger so that
the syringe needle can be kept inside cylinder when the plunger
is pulled back.
This disposable syringe that I have patented as above had some
defects requiring a host of parts and extreme preciseness whereby
creating difficulties in manufacturing. This device has been developed
instead. It is simpler in structure, easier in manufacturing, has
eliminated the possibility of mis-use and requires less number of
parts.
The following refers to FIGS. 1-11.
The safety syringe of the present invention has a cylinder for
injection. Inside the cylinder are piston and plunger. In a syringe
which the dead-end of the cylinder has a syringe needle usually
affixed, cylinder (11), syringe needle (21), syringe needle inserter
(31) and plunger (41) are the parts in structure. At the end of
inserting of the cylinder are a host of projection (13) and incised
grooves (14) arranged alternately. On the inner face of the cylinder
are stopping sill (15) and obstacle (hooking) sill (16) at the rear
end. At the center of the syringe needle inserter (31) is the syringe
needle fixer (32). On the outer face (33) of barrel shaped syringe
needle fixer (32) are number of "L" shaped grooves (34)
for projections (13) to enter. Packing (35) is placed in its rear.
Inside of the rear-end are projections prominence (36) on the top
and bottom. Inside both of the up/down projections aforesaid is
formed the obstacle (hooking) ring sill (37). On the tip of the
plunger (41) where piston (42) is inserted are top/bottom connecting
device (43) which have hooking sills (43'). On the both ends of
the central projection (44) are erected projections (44'). At the
end of the plunger (41) where piston (42) is inserted forms a space
(47). Pressing button (48) at the rear part of the plunger (41)
has a inserting groove (48'). The inserting groove (48') is for
the cap (49) to be inserted to cover the inserting hole (12) of
the cylinder tip.
In order for the plunger (41) to be easily broken at cutting notch
(45), in the fore part of the plunger (41) are many "V"
shaped grooves or holes and at the rear part of the piston (42)
of plunger (41) is formed a stopping ring sill (50).
This device with such structure will act as follows:
Cylinder (11) and the syringe needle inserter (31) are combined
together by thrusting the needle inserter (31) from the rear end
of the cylinder (11) to the inside of the cylinder until the projections
(13) on the inner face of the cylinder (11) insert hole (12) meet
and set in the "V" shaped grooves formed on the outer
face of the barrel shaped needle inserter (31).
Then the piston (42) inserted plunger (41) is pushed into the rear
side of the cylinder (11). Right before the use of the syringe,
syringe needle (21) is fixed in the syringe needle inserter (31)
as usual. Injection is sucked into the cylinder (11) by pulling
the plunger backward. Injection is done to the patient by pushing
the plunger (41).
At the time when the syringe needle inserter (31) is fixed to the
cylinder (11) from the rear toward inner side, it has to be pushed
until the projections (13) of inserting hole (12) of the cylinder
set in toward the circumference direction of the "L" shaped
grooves of the syringe needle inserter (31). At this time, the incised
grooves between projections (13) will help syringe needle inserter
(31) entering into the cylinder (11) by making the cylinder (11)
tip burst open so that the needle inserter (31) can be easily set
in.
The stopping sill (15) of the inner face of the cylinder (11) joints
the rear tip of the syringe needle inserter (31). The packing (35)
inserted in the syringe needle inserter (31) will closely adhere
to the inner face of the cylinder (11).
When the syringe inserter (31) is inserted by force into the inserting
hole (12) of the cylinder (11) tip in order to fix the syringe needle
inserter (31) onto the cylinder's (11) tip, the projections (13)
of the inner face of the cylinder (11) will be hooked on any of
the "L" shaped grooves (34) of the outer face of the syringe
needle inserter (31), that is, on the groove of any location in
circumference direction, but as the syringe needle inserter (31)
turns accordingly when we turn and fix the syringe needle (21) in
the syringe needle inserter (31), the projections (13) erected in
the inserting hole (12) of the cylinder (11) will become to locate
at the last of the "L" shaped grooves as soon as the syringe
needle is fixed in.
Moreover, as the meeting places of the "L" shaped grooves
are not flat but are "U" or "V" shaped, the
projections (13) of cylinder (11) cannot be located on the border
between the "L" shapes.
Like this, the syringe needle inserter (31) and syringe needle
are fixed at the cylinder (11) tip, and by thrusting the plunger
(41) into the cylinder (11), syringe assembly is completed. The
syringe sucks the injection into the cylinder (11) when the plunger
(41) is pulled back. After plucking the needle (21) from the patient
(Ref. FIG. 9) upon completion of injection, if we apply force to
push the plunger (41) (Ref. FIG. 10), piston (42) is being pressed
so as for its volume to become smaller by the space (47) formed
inside of the piston (42), and at the same time, the respective
hooking sills (43') of upper and lower connecting device (43) formed
up and down the plunger (41) is inserted in the obstacle ring sill
(37) of the inner face of the rear part syringe needle inserter
(31), plunger (41) tip and the syringe needle inserter (31) rear
part will be combined together. When the plunger (41) is turned,
the projection (44') erected both sides of the central projection
(44) of the plunger tip will joint the up/down projections (36)
of the rear inner face of the syringe needle inserter (31), and
the turning plunger (41) will turn the syringe needle inserter (31).
The syringe needle inserter (31) which is turned by the plunger
(41) is again turning the "L" shaped grooves (34), then
the projections (13) of the cylinder (11) will turn the straight
line of the "L" shaped grooves (34). When the plunger
is drawn back, the projections (31) will be pushed forward along
the straight lines of "L" shaped grooves, and at the same
time, the needle inserter (31) as well as the syringe needle (21)
which is inserted thereto will be pushed back to inside of cylinder
(11).
Backtracking plunger (41) will retreat until the plunger ring sill
(40) reaches the hooking sill (16), then plunger (41) is to be broken.
Then all the operation comes to an end by trans-inserting the cap
(49) which is inserted in the pressing hole (48) into the inserting
hole (12) in front of the cylinder (11).
In the cap's (49) inserting hold is prepared a ring (circular)
sill and because the ring sill of the cap (49) insert hole is to
meet the projection (13) of the insert hole (12) of cylinder (11),
the cap inserted in the insert hole (12) would not easily come out.
This device is designed to withhold the used syringe needle inside
the cylinder, the main body of syringe, and whereby to prevent the
possible damages which may happen to medical workers including doctors
and nurses as well as a third party from being pricked by the used
syringe needles.
The syringe needs to be dealt with utmost care regardless before
or after use, due to the sharp-pointed needles. A special attention
is required to be paid to the used ones because of the bloodstain.
Especially, because hepatitis and AIDS are infectious to a third
party via blood stain, the syringes used for patients of such disease
must be handled with special attention.
However, as described in this device, if we insert the used syringe
needle into the cylinder and then break the plunger, the syringe
needle will be located inside the cylinder. If we cover the cylinder
with the cap prepared in the rear of the plunger, there is no possibility
at all for the syringe needle inside the cylinder to be exposed
out of the cylinder and can be kept safely in custody until further
process.
If we use this device, we cannot re-use the used syringes. Therefore,
it is very useful device as it can prevent disease caused by the
used syringe needles from being infectious to a third person.
This device is designed to keep the used syringe needle inside
the cylinder prohibiting re-use of the used syringe needles in order
to prevent possible damages for medical workers including doctors
and nurses and a third party alike to be taken from being pricked
by the used syringe needles. The syringe needle, which is fixed
in the syringe needle fixer, is set at the tip of cylinder with
the help of the syringe needle inserter.
Inserting part is composed at the projection of the tip of the
plunger, which is to be put in the cylinder. At the rear end of
the syringe needle fixer is formed the assembling part. The projection
of the plunger joints the syringe needle fixer. When plunger is
drawn back, syringe needle fixer with its needle fixed in will also
be drawn back and kept inside the cylinder. Thus, damages by the
used syringe needle can be prevented. This device is of the safety
syringe which can prevent infectious diseases such as hepatitis
and AIDS.
Some important aspects of the safety syringes according to the
first embodiment are as follows:
It has a cylinder to suck in injection. Piston and plunger are
in the cylinder while the ordinary syringe has the syringe needle
affixed to the syringe, this device has the cylinder (11), syringe
needle (21), syringe needle inserter (31) and plunger respectively
as parts of its structure. At the insert hole (16) of the above
said cylinder (11) tip are a host of projections (13) and incised
grooves (14) arranged alternatively one after another. Cylinder's
(11) inner face has stopping sill and hooking sill in the rear.
At the center of the syringe needle inserter is a syringe needle
fixer to fix syringe needle. Outer barrel shaped outer face of the
syringe needle fixer has a number of "L" shaped grooves
for projections (13) formed on the inner face of the insert hole
(12) to set in. Packing (35) is set in the rear. On the upper and
lower part of the inner face of the rear part are projections (36).
Inside the upper and lower projections (16) is hooking ring sill
(37). At the plunger (41) tip where piston is inserted are top and
bottom joints connecting device which has hooking sill (43'). On
both sides of the central projection (44) inside the top/bottom
joint connecting device. Space (47) is formed at the plunger (41)
tip where piston is inserted in. At the pressing/pushing button
(48) of the rear end of the plunger (41) has the insert groove (48').
In the insert groove (48'), a cap (49) is supposed to be inserted
to cover insert hole (12) of the cylinder tip.
In the following, a safety syringe according to the second aspect
and further aspects of the invention is explained.
This device relates to a safety syringe so as to prevent the pricking
of another person by means of withdrawing a needle in the inside
of a barrel keeping in it after injection and the reuse of a syringe
by means of breaking off a plunger.
The prior single use syringe which a technical method is applied
to in order to prevent the reuse of a used syringe was usual.
But there was the possibility of pricking by a used needle because
the prior single use syringe is left or thrown away, holding the
needle on the syringe. Thus the problem that another person might
be damaged with the used needle could not be solved by the single
use syringe.
That is, some blood is left on the needle after injection. In that
case, if doctor, nurse, medical employee or other person was pricked
by the used needle, they might be infected with the disease of the
patient (such as AIDS, hepatitis and the like) by it. The examples
are actually reported.
This device relates to the safety syringe so as to prevent transmitting
the infectious diseases through the used needle, withdrawing the
used needle into the inside of a barrel and keeping it in a barrel
without removal of the needle, after injection.
As prior patent documents on a safety syringe, there is Utility
Model Announcement #91-4532 and Open Utility Model Announcement
#96-13409 which were applied by this applicant and were announced.
And also this applicant applied for utility model of a safety single
use syringe in Utility Model Application #7783 in 1999.
This device has more simple structure and exact function than prior
syringes which was applied by this applicant before.
The safety syringes that the needle set is fixed to the plunger,
withdrawn into the inside of a barrel and kept in it after injection
are shown in Utility Model Announcement #91-4532 Open Utility Model
#96-13409 and Utility Model Application #7783 which were applied
by this applicant and announced.
The prior single use syringes which were applied for utility model
by this applicant had a problem in manufacturing because those need
a great number of parts and high precision as this device is newly
developed in order to remove the demerits, it needs few number of
parts, the structure is simple, manufacturing is easy and the possibility
of the incorrect operation gets removed.
In the following it is referred to FIGS. 12 to 25.
Structure of Device
Same as general syringe has a barrel which medication is sucked
into, a piston and a plunger in the inside of a barrel.
This safety single use syringe is composed of a barrel (11), a
needle (21), a plunger (41) and a needle inserting device (31) to
which a needle (21) is attached. A number of projections (13) are
in the inside of the front end of an inserting hole (12) of the
above barrel (11), an annular restraining prominence (16) is at
the rear end of a barrel, a needle locking device (32) to attache
a needle (21) is at the center of a needle inserting device (31),
a number of "L" shaped female grooves (34) having the
wide entrances in order to be assembled with a projection (13) located
at an inner surface of an inserting hole (12) of the above cylindrical
barrel (11) are on the outer cylindrical surface (33) of a needle
locking device (32), an O-ring (35) is inserted at the rear of the
grooves, a number of female grooves (37) are in the inside of a
needle inserting device (31), a male extensions (43) having each
restraining prominence (43') are at the front end of a plunger (41)
to be assembled with a piston (42), an empty space (47) is at the
front end of a plunger (41) to be assembled with a piston (42),
a cutting notch (45) is at the front part of a plunger (41) in order
to be easily broken off, an annular stop prominence (50) is at the
rear part of a plunger (41), rear stop projections (51) are at the
longitudinal center of a plunger, an empty space (53) is longitudinally
in the central inside of a plunger (41) between rear stop projections
(51) and cutting notch.
The device having this structure operates as follows:
A needle inserting device (31) is inserted into a barrel from the
back end of a barrel (11) and pushed towards the front end until
a number of projections (18) in the inside of an inserting hold
(12) of a barrel (11) reaches the end of "L" shaped groove
(34) having a wide entrance on the cylindrical outer surface (33)
of a needle inserting device (31), and assembled with a barrel (11).
And then a plunger (41) assembled with a piston (42) is inserted
into a barrel from the back end of a barrel (11) and a needle (21)
is put into a needle inserting device (31) just before using a syringe.
A plunger (41) is pulled back and medication is sucked into the
inside of a barrel (11) as usual. Medication is injected into a
patient's body, a plunger (41) being pushed.
When a needle inserting device (31) is inserted into a barrel (110)
from the back end of a barrel (11) and fixed to a barrel, a needle
inserting device (31) is pushed into a barrel until a number of
projections (13) in the inside of an inserting hole (12) of a barrel
(11) reaches the end of the "L" shaped groove (34) having
the wide entrance on the outer surface of needle inserting device
(31). In this case an annular stop prominence (15) on the inner
surface of a barrel (11) meets the back end of a needle inserting
device (31) and an O-ring (35) inserted into a needle inserting
device (31) clings to the inner cylindrical surface of a barrel
(11) so that sealing is completely kept.
When a needle inserting device (31) is pushed into an inserting
hole (12) at the front end of a barrel (11) and locked, the projections
(13) on the inner circumferential surface of a barrel (11) is positioned
at the back end (the entrance of the groove) of the "L"
shaped female groove (34) having the wide entrance on the outer
circumferential surface of a needle inserting device (31). But when
a needle (21) is put into a needle inserting device (31) and locked,
the male projections (13) in the inside of an inserting hole (12)
of a barrel (11) is positioned at the end of "L" shaped
female groove (34) because both the needle (21) and the needle inserting
device (31) are rotated together.
Thus, a needle inserting device (31) and a needle (21) is at the
front end of a barrel (11) and a plunger (41) is inserted into a
barrel (11) so that the assembly of a syringe is finished. The plunger
(41) is pulled back, the medication is sucked into a barrel and
it is injected to a patient's body, after medication is injected
to a body and a needle (21) is withdrawn from it, as additional
force is applied to a plunger (41) (FIG. 5), a piston (42) which
has an empty space (47) inside is pressed and squeezed. At the same
time each restraining stop projections (43') of a locking device
(43) is locked in the inside of a female groove (37) located at
the outside of a central hole of a needle inserting device (31)
so that the front end of a plunger (41) is connected with the back
end of a needle inserting device (31). Thereafter, if a plunger
is rotated, a needle inserting device (31) is rotated together by
it.
Thus a "L" shaped female groove (34) on the outer surface
of a needle inserting device (31) rotated by a plunger (41) is rotated
together so that projections (13) on the inner circumferential surface
of the front end of a barrel (11), which are positioned circumferentially
in a "L" shaped female groove (34), are rotated until
the straight line of a "L" shaped female grove (34), after
that, when a plunger (41) is pulled back, projections (13) is moved
forward through the straight line of a "L" shaped female
groove (34), and simultaneously a needle inserting device (31) with
an attached needle (21) is moved back into a barrel (11) and kept
inside.
A plunger (41) is moved backwards until a plunger annular prominence
(50) reaches a restraining annular prominence (16) of a barrel.
And then, a plunger is broken off at a cutting notch (45). Thus
the broken plunger (42) is inserted into a barrel from the front
end of a barrel. In other words, a rear restraining stop projection
(51) of a plunger (41) is inserted until it reaches the inside of
a projection (31) located in the inside of a front inserting hole
(12) of a barrel (11). A plunger (41) which is locked in an inserting
hole (12) is not pulled back easily because a rear restraining stop
projection (51) is engaged with a projection (31) in the front end
of an inserting hole.
Consequently, a needle inserting device (31) including a needle
(21) is thoroughly inserted into the inside of a barrel (11). A
needle stored in the inside of a barrel is safely kept in because
an inserting hole (12) is blocked by a broken plunger (41).
Effect of Device
This device can prevent a pricking of doctor, nurse and other medical
employee because a needle used for a patient is inserted into the
inside of a barrel and kept in.
A syringe having a sharp needle should be treated with much care,
whether it is used or not. Especially, in case of a blood-stained
needle used for a patient, it should be treated most carefully.
The diseases such as hepatitis, AIDS and the like can be transmitted
through blood. Therefore, a needle used for such a patient should
be handled with utmost care.
This device has an advantage that a needle is safely kept in a
barrel because a plunger is broken off after a needle of a syringe
is thoroughly inserted into a barrel. A broken-off plunger is inserted
into a barrel through an inserting hole. An inserting hole is blocked
with a broken plunger so that a needle can be kept in and treated
safely.
Thus this is a useful device which makes a used syringe not to
be reused and prevents infectious diseases from spreading.
This relates to a device for preventing that disposable syringe
is reused and that doctors, nurses, medical employees or others
are pricked by the used needle by means of inserting it into a barrel
after injection. The needle is attached to the front of a barrel
with a needle inserting device, an inserting part is made on male
extensions in the front end of the plunger which is inserted into
a barrel and a connecting part is made in the back end of a needle
inserting device. A male extension of a plunger is assembled with
a needle locking device and a needle inserting device which a needle
is attached to is inserted into a barrel when a plunger is pulled
back. A needle inserting device is kept in the inside of a barrel.
Therefore, user doesn't be pricked by the used needle. Consequently,
this safety syringe can prevent infectious diseases such as hepatitis
and AIDS from spreading.
Some important aspects of the safety syringe according to the second
embodiment are as follows:
This safety single use syringe is composed of a barrel (11), a
needle (21), a plunger (41) and a needle inserting device (31),
same as a general syringe which has a barrel into which the liquid
medicine is sucked, a piston and a plunger inside the barrel, and
a needle is put on the front tip of the barrel. There s a number
of projections (13) in the inside of the front end of an inserting
hole (12) of the above barrel (11), the circular stop prominence
(15) at the inner surface of a barrel (11), a circular restraining
prominence (16) inside the rear end of a barrel, a needle fixing
device (32) to insert a needle (21) at the center of a needle inserting
device (31), a number of "L" shaped grooves (34) with
the wide entrances at an outer surface (33) of a cylindrical part
of a needle fixing device (32) in order to be assembled with a projection
(13) located at an inner surface of an inserting hole (12) of the
above cylindrical barrel (11), an O-ring (35) in the rear of the
groves, a number of the inserting grooves (37), a connecting device
(43) of upper and lower part with restraining prominences (43')
at the front end of a plunger (41) to be assembled with a piston
(42), an empty part (47) at the front end of a plunger (41) to be
assembled with a piston (42), a cutting notch (45) at the front
part of a plunger (41) in order to be easily broken off, a circular
stop prominence (50) at the front part of a plunger (41) reaching
to the rear of a piston (42), a rear stop projection (51) at the
longitudinal center of a plunger, an empty part longitudinally from
a rear stop projection (51) to a cutting notch (45) in the central
inside of a plunger.
A relevant difference between the first and the second embodiment
is as follows:
According to the first embodiment, the plunger (41) has a cap (49),
which serves to close the front hole of the cylinder (11) after
injection, i.e. after retraction of the needle (21) into the cylinder
(cp. FIGS. 10 and 11).
According to the second embodiment, a part of the plunger (11)
itself serves (after breaking the plunger) to close the front hole
of the cylinder (11) after injection, i.e. after retraction of the
needle (21) into the cylinder. To close the front hole, the part
of the plunger is inserted into the cylinder (cp. FIGS. 16 and 18)
Accordingly, the costs for the manufacturing of the cap (e.g. the
cost for providing a mold) are saved.
Besides this difference, the general structure and functioning
of the first and second embodiment are more or less the same.
In the above specification, the terms barrel and cylinder are used
as synonyms. The needle inserting device or needle inserter (31)
may as well be termed needle holder.
Third Embodiment
Referring now to FIGS. 26-32 a third embodiment of the present
invention may be described. Referring to FIG. 26 shown disassembled
are portions of a safety syringe including a hollow needle 21 a
thin-walled cylinder or barrel 11 (the forward end being shown),
a needle holder 61 and a plunger 71. This embodiment includes an
improved connection between the needle holder 61 and plunger 71.
Accordingly, the aft portion of the needle holder 61 and forward
portion of the plunger 71 are different from the safety syringes
described above.
As best shown in FIG. 26 the aft portion of the needle holder
61 includes a generally circular opening 64 leading to a generally
cylindrically cavity 66 having an inner surface 65. Around the circular
opening 64 are a pair of latching members or tabs 69 which are rounded
and project slightly into and aft of the circular opening 65. Inside
the cylindrically cavity 66 are a pair of stops or upstanding webs
68 from the inner surface 65. FIGS. 29 and 30 illustrate the aft
end of the needle holder 61 in greater detail, including the latching
members or tabs 69 and the stops or upstanding webs 68.
Next the corresponding structure in the forward end of the plunger
71 is described. The forward end of the piston 72 includes an anchor
member 74 consisting of a pair of flukes 76. The flukes 76 and the
anchor member 74 are sized to be received through the circular opening
64 in the aft portion of the needle holder 61 and into the cylindrical
cavity 66 in a close clearance or slight interference fit. FIG.
31 illustrates the plunger 71 anchor member 74 inside the needle
holder 61 cylindrical cavity 66.
Having described the structure of the third embodiment, now its
operation and use is described, in particular the improved coupling
of the plunger 71 and needle holder 61. Also referring to FIG. 27
upon dispensing the fluid contained in the cylinder or barrel 11
the forward portion of the plunger 71 or piston 72 is near the needle
holder 61. Further pushing the plunger 71 forward causes the anchor
member 74 to travel through the circular opening 65 lodge itself
inside the cylindrical cavity 66 of the needle holder 61. See FIG.
32. Then rotating the plunger 71 clockwise causes the anchor member
74 flukes 76 to rotate until they contact the stops or upstanding
webs 68. At this point the flukes 76 are housed behind the latching
members or tabs 69 thereby coupling the plunger 71 and needle holder
61 together. If the plunger 71 and needle holder 61 were somehow
inadvertently coupled, merely reversing the above steps, i.e. rotating
counterclockwise and pulling the plunger 71 will separate the two.
The typical next step as described above would be continued clockwise
rotation of the plunger 71 causing the needle holder 61 to turn
as the projections 13 at the forward end of the cylinder or barrel
11 ride inside the L-shaped slots 61 at the forward portion of the
needle holder 61. Then it is possible to pull the hollow needle
21 and needle holder 61 aft until the hollow needle 21 is entirely
inside the cylinder or barrel 11. Lastly, the plunger 71 sticking
out the aft end of the cylinder or barrel may be broken off at a
weakened section of the plunger shaft, thereby leaving the hollow
needle 21 inside the cylinder or barrel 11 and preventing reuse
of the device. A removable cap 49 from the aft end of the plunger
71 may be placed over the forward end of the cylinder or barrel
11. |