CA2408757C - Disposable syringe - Google Patents
Disposable syringe Download PDFInfo
- Publication number
- CA2408757C CA2408757C CA 2408757 CA2408757A CA2408757C CA 2408757 C CA2408757 C CA 2408757C CA 2408757 CA2408757 CA 2408757 CA 2408757 A CA2408757 A CA 2408757A CA 2408757 C CA2408757 C CA 2408757C
- Authority
- CA
- Canada
- Prior art keywords
- surrounding
- segment
- edge portion
- disposable syringe
- surrounding edge
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
- A61M5/3205—Apparatus for removing or disposing of used needles or syringes, e.g. containers; Means for protection against accidental injuries from used needles
- A61M5/321—Means for protection against accidental injuries by used needles
- A61M5/322—Retractable needles, i.e. disconnected from and withdrawn into the syringe barrel by the piston
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/178—Syringes
- A61M5/31—Details
- A61M5/315—Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms
- A61M5/31511—Piston or piston-rod constructions, e.g. connection of piston with piston-rod
- A61M2005/31516—Piston or piston-rod constructions, e.g. connection of piston with piston-rod reducing dead-space in the syringe barrel after delivery
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/50—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests having means for preventing re-use, or for indicating if defective, used, tampered with or unsterile
- A61M5/5066—Means for preventing re-use by disconnection of piston and piston-rod
- A61M2005/5073—Means for preventing re-use by disconnection of piston and piston-rod by breaking or rupturing the connection parts
Abstract
A disposable syringe has a needle seat with an upper segment adapted to be fitted with a needle unit, and a lower segment retained in a passage of a barrel. A plunger has a stem portion movable in the passage, a surrounding engaging portion in sealing contact with the passage so as to be moved by the stem portion to a position of use, and a head which is moved towards and which is held by a grip segment in the needle seat when the surrounding engaging portion is depressed by an edge portion of the needle seat by virtue of a continuing depression force of the plunger, thereby permitting the needle seat to be brought into the passage for disposal.
Description
DISPOSABLE SYRINGE
FIELD OF THE INVENTION
This invention relates to a disposable syringe, more particularly to a disposable syringe which enables a needle unit S to be retracted within a barrel after use for safe disposal.
BRIEF DESCRIPTION OF THE DRAWINGS
Other features and advantages of the present invention will become apparent in the following detailed description of the preferred embodiments of the invention, with reference to the accompanying drawings, in which:
Fig. 1 is a longitudinal sectional view of a conventional disposable syringe assembly;
Fig. 2 is an exploded perspective view of a first preferred embodiment of a disposable syringe according to this invention for use with a needle unit to form a syringe assembly;
Fig. 3 is a perspective view of the syringe assembly according to the first preferred embodiment;
Fig. 4 is a longitudinal sectional view showing the syringe assembly during use;
Fig. 5 is a longitudinal sectional view showing the syringe assembly in a state of use;
Fig. 6 is a longitudinal sectional view showing the syringe assembly in a state in which a head of a plunger is held by a grip segment of a needle seat;
Fig. 7 is a longitudinal sectional view showing the syringe assembly in a retracted state;
Fig. 8 is a longitudinal sectional view showing a second preferred embodiment of a disposable syringe according to this invention for use with a needle unit to form a syringe assembly;
Fig. 9 is a longitudinal sectional view showing the syringe assembly according to the second preferred embodiment in a state in which a head of a plunger is held by a grip segment of a needle seat;
Fig. 10 is a longitudinal sectional view showing the syringe assembly in a retracted state;
Fig. 11 is an exploded longitudinal sectional view showing a third preferred embodiment of a disposable syringe according to this invention for use with a needle unit to form a syringe assembly;
Fig. 12 is a longitudinal sectional view showing the syringe assembly in a retracted state;
Fig. 13 is a fragmentary longitudinal sectional view showing a fourth preferred embodiment of a disposable syringe according to this invention for use with a needle unit;
Fig. 14 is a fragmentary longitudinal sectional view showing a fifth preferred embodiment of a disposable syringe according to this invention for use with a needle unit; and Fig. 15 is a fragmentary longitudinal sectional view showing a sixth preferred embodiment of a disposable syringe according to this invention for use with a needle unit.
OF THE INVENTION
Referring to Fig. 1, a conventional disposable syringe assembly 10 is shown to include a barrel 11, a plunger 12 and a needle unit 13. The barrel 11 has an open neck end portion 111 to which a needle hub 131 of the needle unit 13 is attached, and an open rear end from which the plunger 12 is slidably inserted into the barrel 11. A forward end 121 of the plunger 12 is snugly fitted in, but is nevertheless slidable along the inner surface S of the barrel 11 through a distance (L) . The needle unit 13 further has a needle 132 extending from the needle hub 131, and a cap 133 with an open end which is fitted around an outer edge of the needle hub 131, with the needle 132 enclosed within the cap 133.
The cap 133 is removed from the needle hub 131 when the syringe assembly 10 is to be used, and is sleeved back after use to ensure that the needle 132 is covered. Thereafter, the needle unit 13 is detached from the barrel 11 along with the cap 133 covering the needle 132.
However, the medical or nursing personnel who has to handle the conventional disposable syringe assembly 10, is exposed to the risk of being pricked by the needle 132 when sleeving the cap 133 back on the needle hub 131 after using the disposable syringe assembly 10 since the dimension of the open end of the cap 133 is relatively small. Moreover, as forward movement of the for4vard end 121 of the plunger 12 terminates at the point (P1) , some medicine or blood may remain within the neck end portion 111, which can cause contamination to the personnel who is unfortunately pricked by the needle 132.
SU1~1AR7C OF TFIE INVENTION
The object of the present invention is to provide a disposable syringe which provides greater safety in use and which eliminates the aforesaid drawback of the prior art.
FIELD OF THE INVENTION
This invention relates to a disposable syringe, more particularly to a disposable syringe which enables a needle unit S to be retracted within a barrel after use for safe disposal.
BRIEF DESCRIPTION OF THE DRAWINGS
Other features and advantages of the present invention will become apparent in the following detailed description of the preferred embodiments of the invention, with reference to the accompanying drawings, in which:
Fig. 1 is a longitudinal sectional view of a conventional disposable syringe assembly;
Fig. 2 is an exploded perspective view of a first preferred embodiment of a disposable syringe according to this invention for use with a needle unit to form a syringe assembly;
Fig. 3 is a perspective view of the syringe assembly according to the first preferred embodiment;
Fig. 4 is a longitudinal sectional view showing the syringe assembly during use;
Fig. 5 is a longitudinal sectional view showing the syringe assembly in a state of use;
Fig. 6 is a longitudinal sectional view showing the syringe assembly in a state in which a head of a plunger is held by a grip segment of a needle seat;
Fig. 7 is a longitudinal sectional view showing the syringe assembly in a retracted state;
Fig. 8 is a longitudinal sectional view showing a second preferred embodiment of a disposable syringe according to this invention for use with a needle unit to form a syringe assembly;
Fig. 9 is a longitudinal sectional view showing the syringe assembly according to the second preferred embodiment in a state in which a head of a plunger is held by a grip segment of a needle seat;
Fig. 10 is a longitudinal sectional view showing the syringe assembly in a retracted state;
Fig. 11 is an exploded longitudinal sectional view showing a third preferred embodiment of a disposable syringe according to this invention for use with a needle unit to form a syringe assembly;
Fig. 12 is a longitudinal sectional view showing the syringe assembly in a retracted state;
Fig. 13 is a fragmentary longitudinal sectional view showing a fourth preferred embodiment of a disposable syringe according to this invention for use with a needle unit;
Fig. 14 is a fragmentary longitudinal sectional view showing a fifth preferred embodiment of a disposable syringe according to this invention for use with a needle unit; and Fig. 15 is a fragmentary longitudinal sectional view showing a sixth preferred embodiment of a disposable syringe according to this invention for use with a needle unit.
OF THE INVENTION
Referring to Fig. 1, a conventional disposable syringe assembly 10 is shown to include a barrel 11, a plunger 12 and a needle unit 13. The barrel 11 has an open neck end portion 111 to which a needle hub 131 of the needle unit 13 is attached, and an open rear end from which the plunger 12 is slidably inserted into the barrel 11. A forward end 121 of the plunger 12 is snugly fitted in, but is nevertheless slidable along the inner surface S of the barrel 11 through a distance (L) . The needle unit 13 further has a needle 132 extending from the needle hub 131, and a cap 133 with an open end which is fitted around an outer edge of the needle hub 131, with the needle 132 enclosed within the cap 133.
The cap 133 is removed from the needle hub 131 when the syringe assembly 10 is to be used, and is sleeved back after use to ensure that the needle 132 is covered. Thereafter, the needle unit 13 is detached from the barrel 11 along with the cap 133 covering the needle 132.
However, the medical or nursing personnel who has to handle the conventional disposable syringe assembly 10, is exposed to the risk of being pricked by the needle 132 when sleeving the cap 133 back on the needle hub 131 after using the disposable syringe assembly 10 since the dimension of the open end of the cap 133 is relatively small. Moreover, as forward movement of the for4vard end 121 of the plunger 12 terminates at the point (P1) , some medicine or blood may remain within the neck end portion 111, which can cause contamination to the personnel who is unfortunately pricked by the needle 132.
SU1~1AR7C OF TFIE INVENTION
The object of the present invention is to provide a disposable syringe which provides greater safety in use and which eliminates the aforesaid drawback of the prior art.
According to this invention, the disposable syringe includes a barrel having an inner surrounding barrel wall surface which surrounds an axis and which confines a passage. The passage has lower and upper open ends disposed opposite to each other in a longitudinal direction parallel to the axis. The inner surrounding barrel wall surface includes a larger-diameter segment and a smaller-diameter segment which are disposed proximate to the lower and upper open ends, respectively, and which cooperatively form a surrounding shoulder portion therebetween.
A tubular needle seat is insertable into the passage from the lower open end toward the upper open end, and includes a lower surrounding edge portion disposed to abut against the first surrounding shoulder portion, an upper surrounding edge portion disposed opposite to the lower surrounding edge portion in the longitudinal direction, and a surrounding seat wall interposed therebetween. The surrounding seat wall has an inner tubular wall surface which surrounds the axis to confine a duct and which forms a grip segment, and an outer tubular wall surface. The outer tubular wall surface includes a lower segment proximate to the lower surrounding edge portion, and an upper segment disposed opposite to the lower segment and proximate to the upper surrounding edge portion. When the upper surrounding edge portion is forced to extend toward the upper open end after the tubular needle seat is inserted into the passage, the lower segment will be brought to a position of use, where the lower segment engages and is retained at the smaller-diameter segment by virtue of a first friction force generated therebetween while the lower surrounding edge portion abuts against the surrounding shoulder portion. In addition, when the upper surrounding edge portion is moved against the first friction force toward the lower open 5 end passing the larger-diameter segment, the needle seat will be brought to a retracted position, where the lower segment and the lower surrounding edge portion are remote from the smaller-diameter segment and the first surrounding shoulder portion, respectively. The outer tubular wall surface is adapted to be fitted with a needle unit.
A plunger includes a stem portion which is disposed to be movable in the passage and which has inner and outer segments opposite to each other in the longitudinal direction. The outer segment extends outwardly of the lower open end of the passage .
An actuated end extends from the outer segment so as to be actuated to move the stem portion along the passage . A surrounding engaging portion is retainingly sleeved on the inner segment by virtue of a second friction force, and is in sealing contact with and is slidable relative to the larger-diameter segment so as to be moved with the stem portion to the position of use . A head extends from the inner segment toward the grip segment. When the surrounding engaging portion is brought by the inner segment to engage the lower surrounding edge portion and is depressed by the lower surrounding edge portion by virtue of a third force that is generated as a consequence of continuing movement of the inner segment towards the smaller-diameter segment and that third force is greater than the second friction force, the surrounding engaging portion is retained by the lower surrounding edge portion to thereby permit the head to move towards the grip segment of the tubular needle seat and to be held by virtue of a fourth friction force that is greater than the first friction force.
DETAILED DESCRIPTION OF THE PREFERRED E~ODIMENTS
Before the present invention is described in greater detail, it should be noted that same reference numerals have been used to denote like elements throughout the specification.
Referring to Figs. 2, 3 and 4, the first preferred embodiment of the disposable syringe according to the present invention is shown to be used with a needle unit 40 to form a syringe assembly.
The needle unit 40 includes a needle hub 42 and a needle 41 which is securely affixed to the needle hub 42. The needle hub 42 has a sleeved portion 423 with a plurality of longitudinally extending frictional ribs 421 formed thereon. A tip protector 43 has an internal sleeve end 431 which is configured to be sleeved on the sleeved portion 423 for shielding the needle 41 and which has a plurality of longitudinally extending frictional ribs 433 for engaging the frictional ribs 421.
The syringe in this embodiment is shown to comprise a barrel 20, a tubular needle seat 30, and a plunger 50.
The barrel 20 has an inner surrounding barrel wall surface 221 which surrounds an axis (X) and which confines a passage 21.
The passage 21 has lower and upper open ends 211,212 which are disposed opposite to each other in a longitudinal direction parallel to the axis (X). The inner surrounding barrel wall surface 221 includes a larger-diameter segment 213 arid a smaller-diameter segment 214 which are disposed proximate to the lower and upper open ends 211,212, respectively, and which cooperatively form a first surrounding shoulder portion 215 therebetween. A finger flange 23 is disposed on an outer S surrounding barrel wall surface 222 of the barrel 20 at the lower open end 211. The smaller-diameter segment 214 is formed with a retaining groove 223 proximate to the f first surrounding shoulder portion 215, and an axially extending friction spline portion 216 remote from the first surrounding shoulder portion 215. A
protruding ring 217 is formed on and projects inwardly and radially from the larger-diameter segment 213 adjacent to the lower open end 211.
The tubular needle seat 30 is disposed to be insertable into the passage 21 from the lower open end 211 toward the upper open end 212. The needle seat 30 includes a lower surrounding edge portion 33 disposed to abut against the first surrounding shoulder portion 215 and having an outer surrounding surface 333 which abuts sealingly against the larger-diameter segment 213 , an upper surrounding edge portion 321 disposed opposite to the lower surrounding edge portion 33 in the longitudinal direction, and a surrounding seat wall 32 interposed therebetween.
The seat wall 32 has an inner tubular wall surface 324 which surrounds the axis (X) to confine a duct 31. The duct 31 has a diameter that gradually decreases from the lower surrounding edge portion 33 to the upper surrounding edge portion 321. The inner tubular wall surface 324 forms a grip segment . In this embodiment, the grip segment includes a concave portion 326 which extends inwardly from the inner tubular wall surface 324 in radial directions relative to the axis (X) to form a second surrounding shoulder portion 329 that is adjacent to the lower surrounding edge portion 33.
The seat wall 32 further has an outer tubular wall surface 325 which includes lower and upper segments 322,323. The lower segment 322 is proximate to the lower surrounding edge portion 33, and has a retaining protrusion 327 formed thereon. When the upper surrounding edge portion 321 is forced to extend outwardly of the upper open end 212 of the barrel 20 after the tubular needle seat 30 is inserted into the passage 21, the lower segment 322 will be brought to a position of use, as shown in Fig. 4, where the lower segment 322 engages and is retained at the smaller-diameter segment 214 by virtue of a first friction force generated as a result of retaining engagement of the retaining protrusion 327 in the retaining groove 223, while an upper edge surface 331 of the lower surrounding edge portion 33 abuts against the first surrounding shoulder portion 215 of the barrel 20. The lower segment 322 further has an axially extending friction spline portion 328 which cooperates with the friction spline portion 216 of the smaller-diameter segment 214 to fornn a spline member so as to prevent relative rotation between the needle seat 30 and the barrel 20. The upper segment 323 is disposed opposite to the lower segment 322 and proximate to the upper surrounding edge portion 321, and is adapted to be sleeved over by the needle hub 42 of the needle unit 40 so as to communicate the duct 31 of the needle seat 30 with the needle hub 42.
The plunger 50 includes a stem portion 50a which is movable in the passage 21 of the barrel 20. The stem portion 50a has a plurality of wing plates 53 angularly displaced from one another, a surrounding flange 51 disposed on upper edges of the wing plates S 53, a connecting shank 54 extending from the surrounding flange 51, and a retaining protrusion 542 . The wing plates 53 are tapered downwardly. On the other hand, the stem portion 50a includes inner and outer segments 502,501 opposite to each other in the longitudinal direction. The outer segment 501 extends outwardly of the lower open end 211 of the barrel 20. An actuated end 52, which is a thumb rest, extends from the outer segment 501 so as to be actuated to move the stem portion 50a along the passage 21.
The plunger 50 further includes a head 50b which has a tapered surrounding abutting portion 541 that extends from the retaining protrusion 542 of the inner segment 502 toward the grip segment of the needle seat 30, and a spindle portion 55 which extends upwardly from the surrounding abutting portion 541 along the axis (X) and which terminates at two split halves 552,553 that are spaced apart from each other in a direction transverse to the longitudinal direction with a concave space 551 inbetween. The split halves 552,553 respectively have upper terminal anchoring edges 554,555. Preferably, the spindle portion 55 has an outer diameter which decreases from the surrounding abutting portion 541 toward the split halves 552,553. Moreover, the surrounding abutting portion 541 and the retaining protrusion 542 are configured to be substantially hollow so as to provide greater flexibility.
A deformable surrounding engaging portion 60, preferably made of an elastic material, is retainingly sleeved on the whole retaining protrusion 542 of the inner segment 502 and a portion 5 of the surrounding abutting portion 541 to generate a second friction force. The surrounding engaging portion 60 has upper and lower end faces 64,65 opposite to each other in the longitudinal direction and proximate to and distal from the lower surrounding edge portion 33 of the needle seat 30, respectively, 10 and an outer surrounding surface 63 disposed therebetween. The lower end face 65 is distal from the surrounding flange 51 by a space (S) . The outer surrounding surface 63 sealingly contacts and is slidable relative to the larger-diameter segment 213 of the barrel 20 so as to be moved with the stem portion 50a.
Preferably, the outer surrounding surface 63 is concaved toward the axis (X) to decrease contact area between the outer surrounding surface 63 and the larger-diameter segment 213 so as to facilitate sliding movement of the surrounding engaging portion 60 relative to the larger-diameter segment 213.
With reference to Fig. 5, in use, the plunger 50 is pressed forwardly to push the upper end face 64 of the surrounding engaging portion 60 to abut against a lower edge surface 332 of the lower surrounding edge portion 33 of the needle seat 30. Since the spindle portion 55 is configured to be tapered upwardly and to match with the inner tubular wall surface 324 of the needle seat 30, drug solution in the passage 21 can almost be completely injected via the needle unit 40.
Subsequently, referring to Fig. 6, when the plunger 50 is further moved forward by a third force towards the smaller-diameter segment 214 against the second friction force between the inner segment 502 and the surrounding engaging portion 60, the surrounding engaging portion 60 is deformed by the lower surrounding edge portion 33, thereby decreasing the space (S) and permitting the surrounding abutting portion 541 of the head 50b to move in the concave portion 326 of the needle seat 30 to abut against the second surrounding shoulder portion 329.
Meanwhile, the split halves 552,553 of the spindle portion 55 are pressed by the inner tubular wall surface 324 to move towards each other against a biasing action when the split halves 552 , 553 are moved towards the upper surrounding edge portion 321.
Once the split halves 552,553 are moved beyond the upper surrounding edge portion 321, the upper terminal anchoring edges 554,555 will engage the upper surrounding edge portion 321 to generate a friction force that combines with the friction force between the surrounding abutting portion 541 and the second surrounding shoulder portion 329 to form a fourth friction force that is greater than the first friction force between the retaining protrusion 327 and the retaining groove 223.
After use, referring to Fig. 7, the outer segment 501 of the plunger 50 is pulled backward to be remote from the finger flange 23 so that the needle seat 30, on which the used needle unit 40 is mounted, is retracted into the passage 21 via the upper open end 212 to bring the upper surrounding edge portion 321 to a retracted position. When the surrounding flange 51 abuts against the protruding ring 217, further movement of the plunger 50 is prevented, thereby restraining the surrounding engaging portion 60 from being moved out of the lower open end 211. In this state, the used needle unit 40 can be enclosed in the passage 21 of the barrel 20 for disposal.
Consequently, chances that the user may be accidentally pricked or pierced by the needle 41 are slim. The safety in use and disposal is thus enhanced.
Furthermore, the wing plates 53 at the inner segment 502 have a weakening area 531 disposed proximate to the surrounding flange 51. As such, when the plunger 50 is retracted to push the surrounding flange 51 to abut against the protruding ring 217, the weakening area 531 extends outwardly of the lower open end 211 so as to ease breaking of the stem portion 50a off the plunger 50 at the weakening area 531 for convenient disposal.
Ref erring to Fig . 8 , the second pref erred embodiment of the disposable syringe according to this invention is shown to be similar to the aforesaid embodiment in construction. The differences therebetween reside in that the spindle portion in the aforesaid embodiment is dispensed with. An elastic surrounding engaging portion 60 is retainingly sleeved on the whole retaining protrusion 742 and a portion of the surrounding abutting portion 741. As such, when the surrounding engaging portion 60 is brought by the stem portion 73 of the plunger 70 upwardly to engage and to be depressed by the lower surrounding edge portion 33 of the needle seat 30, the surrounding engaging portion 60 is retained by the lower surrounding edge portion 33, thereby permitting the surrounding abutting portion 741 to be retained in the concave portion 326, as shown in Fig. 9. Hence, the needle seat 30 and the needle unit 40 can be retracted into the passage 21 of the barrel 20 after an injection procedure to permit breaking of the stem portion 73 of the plunger 70 at a weakening area 731 for safe disposal, as shown in Fig. 10.
Referring to Figs . 11 and 12 , the third pref erred embodiment of the disposable syringe according to this invention is shown to be similar to the aforesaid embodiments in construction. The differences therebetween reside in that a tubular needle seat 30 has a duct 31 with a relatively small diameter at the upper segment 323 so as to engage fittingly the needle 41. Thus, the needle hub 42 can be eliminated.
Moreover, a barrel 20 has an outer surrounding wall surface 222 with a sleeved portion 2221 which is disposed proximate to the upper open end 212 to replace the sleeved portion 423 shown in Fig. 2, and which has a plurality of friction ribs 224 formed thereon. Thus, a tip protector 43, which has a plurality of frictional ribs 433 formed on an internal sleeve end 431 thereof, can be sleeved f fittingly on the sleeved portion 2221 for shielding the needle 41.
In the syringe assembly of this embodiment, the number of components is decreased. Similarly, the needle seat 30 and the needle 41 can be retracted into the passage 21 of the barrel 20 after an injection procedure.
Referring to Fig. 13, the fourth preferred embodiment of the disposable syringe with a similar construction of the aforesaid embodiments, is used for an extremely small injection volume, such as 1 ml. Thus, the dimensions of the barrel 20, the needle seat 30, the needle 41, the plunger 70, and the deformable surrounding engaging portion 60 are smaller than those of the aforesaid embodiments.
Referring to Figs. 14 and 15, the fifth and sixth preferred embodiments of the disposable syringe according to this invention are shown to be similar to the third and fourth embodiments in construction, respectively. The differences therebetween reside in that the upper open end 212 has a surrounding edge wall 219 which extends from the smaller-diameter segment 214 of the inner surrounding barrel wall surface 221 of the barrel 20 toward the axis (X) and which confines a through hole 210 that surrounds the axis (X) . As such, the needle 41 can pass through the through hole 210 and outwardly of the upper open end 212. The sixth preferred embodiment shown in Fig. 15 is similar to the fifth preferred embodiment in construction, but is used for an extremely small injection volume, such as 1 ml.
While the present invention has been described in connection with what is considered the most practical and preferred embodiments, it is understood that this invention is not limited to the disclosed embodiments but is intended to cover various arrangements included within the spirit and scope of the broadest interpretations and equivalent arrangements.
A tubular needle seat is insertable into the passage from the lower open end toward the upper open end, and includes a lower surrounding edge portion disposed to abut against the first surrounding shoulder portion, an upper surrounding edge portion disposed opposite to the lower surrounding edge portion in the longitudinal direction, and a surrounding seat wall interposed therebetween. The surrounding seat wall has an inner tubular wall surface which surrounds the axis to confine a duct and which forms a grip segment, and an outer tubular wall surface. The outer tubular wall surface includes a lower segment proximate to the lower surrounding edge portion, and an upper segment disposed opposite to the lower segment and proximate to the upper surrounding edge portion. When the upper surrounding edge portion is forced to extend toward the upper open end after the tubular needle seat is inserted into the passage, the lower segment will be brought to a position of use, where the lower segment engages and is retained at the smaller-diameter segment by virtue of a first friction force generated therebetween while the lower surrounding edge portion abuts against the surrounding shoulder portion. In addition, when the upper surrounding edge portion is moved against the first friction force toward the lower open 5 end passing the larger-diameter segment, the needle seat will be brought to a retracted position, where the lower segment and the lower surrounding edge portion are remote from the smaller-diameter segment and the first surrounding shoulder portion, respectively. The outer tubular wall surface is adapted to be fitted with a needle unit.
A plunger includes a stem portion which is disposed to be movable in the passage and which has inner and outer segments opposite to each other in the longitudinal direction. The outer segment extends outwardly of the lower open end of the passage .
An actuated end extends from the outer segment so as to be actuated to move the stem portion along the passage . A surrounding engaging portion is retainingly sleeved on the inner segment by virtue of a second friction force, and is in sealing contact with and is slidable relative to the larger-diameter segment so as to be moved with the stem portion to the position of use . A head extends from the inner segment toward the grip segment. When the surrounding engaging portion is brought by the inner segment to engage the lower surrounding edge portion and is depressed by the lower surrounding edge portion by virtue of a third force that is generated as a consequence of continuing movement of the inner segment towards the smaller-diameter segment and that third force is greater than the second friction force, the surrounding engaging portion is retained by the lower surrounding edge portion to thereby permit the head to move towards the grip segment of the tubular needle seat and to be held by virtue of a fourth friction force that is greater than the first friction force.
DETAILED DESCRIPTION OF THE PREFERRED E~ODIMENTS
Before the present invention is described in greater detail, it should be noted that same reference numerals have been used to denote like elements throughout the specification.
Referring to Figs. 2, 3 and 4, the first preferred embodiment of the disposable syringe according to the present invention is shown to be used with a needle unit 40 to form a syringe assembly.
The needle unit 40 includes a needle hub 42 and a needle 41 which is securely affixed to the needle hub 42. The needle hub 42 has a sleeved portion 423 with a plurality of longitudinally extending frictional ribs 421 formed thereon. A tip protector 43 has an internal sleeve end 431 which is configured to be sleeved on the sleeved portion 423 for shielding the needle 41 and which has a plurality of longitudinally extending frictional ribs 433 for engaging the frictional ribs 421.
The syringe in this embodiment is shown to comprise a barrel 20, a tubular needle seat 30, and a plunger 50.
The barrel 20 has an inner surrounding barrel wall surface 221 which surrounds an axis (X) and which confines a passage 21.
The passage 21 has lower and upper open ends 211,212 which are disposed opposite to each other in a longitudinal direction parallel to the axis (X). The inner surrounding barrel wall surface 221 includes a larger-diameter segment 213 arid a smaller-diameter segment 214 which are disposed proximate to the lower and upper open ends 211,212, respectively, and which cooperatively form a first surrounding shoulder portion 215 therebetween. A finger flange 23 is disposed on an outer S surrounding barrel wall surface 222 of the barrel 20 at the lower open end 211. The smaller-diameter segment 214 is formed with a retaining groove 223 proximate to the f first surrounding shoulder portion 215, and an axially extending friction spline portion 216 remote from the first surrounding shoulder portion 215. A
protruding ring 217 is formed on and projects inwardly and radially from the larger-diameter segment 213 adjacent to the lower open end 211.
The tubular needle seat 30 is disposed to be insertable into the passage 21 from the lower open end 211 toward the upper open end 212. The needle seat 30 includes a lower surrounding edge portion 33 disposed to abut against the first surrounding shoulder portion 215 and having an outer surrounding surface 333 which abuts sealingly against the larger-diameter segment 213 , an upper surrounding edge portion 321 disposed opposite to the lower surrounding edge portion 33 in the longitudinal direction, and a surrounding seat wall 32 interposed therebetween.
The seat wall 32 has an inner tubular wall surface 324 which surrounds the axis (X) to confine a duct 31. The duct 31 has a diameter that gradually decreases from the lower surrounding edge portion 33 to the upper surrounding edge portion 321. The inner tubular wall surface 324 forms a grip segment . In this embodiment, the grip segment includes a concave portion 326 which extends inwardly from the inner tubular wall surface 324 in radial directions relative to the axis (X) to form a second surrounding shoulder portion 329 that is adjacent to the lower surrounding edge portion 33.
The seat wall 32 further has an outer tubular wall surface 325 which includes lower and upper segments 322,323. The lower segment 322 is proximate to the lower surrounding edge portion 33, and has a retaining protrusion 327 formed thereon. When the upper surrounding edge portion 321 is forced to extend outwardly of the upper open end 212 of the barrel 20 after the tubular needle seat 30 is inserted into the passage 21, the lower segment 322 will be brought to a position of use, as shown in Fig. 4, where the lower segment 322 engages and is retained at the smaller-diameter segment 214 by virtue of a first friction force generated as a result of retaining engagement of the retaining protrusion 327 in the retaining groove 223, while an upper edge surface 331 of the lower surrounding edge portion 33 abuts against the first surrounding shoulder portion 215 of the barrel 20. The lower segment 322 further has an axially extending friction spline portion 328 which cooperates with the friction spline portion 216 of the smaller-diameter segment 214 to fornn a spline member so as to prevent relative rotation between the needle seat 30 and the barrel 20. The upper segment 323 is disposed opposite to the lower segment 322 and proximate to the upper surrounding edge portion 321, and is adapted to be sleeved over by the needle hub 42 of the needle unit 40 so as to communicate the duct 31 of the needle seat 30 with the needle hub 42.
The plunger 50 includes a stem portion 50a which is movable in the passage 21 of the barrel 20. The stem portion 50a has a plurality of wing plates 53 angularly displaced from one another, a surrounding flange 51 disposed on upper edges of the wing plates S 53, a connecting shank 54 extending from the surrounding flange 51, and a retaining protrusion 542 . The wing plates 53 are tapered downwardly. On the other hand, the stem portion 50a includes inner and outer segments 502,501 opposite to each other in the longitudinal direction. The outer segment 501 extends outwardly of the lower open end 211 of the barrel 20. An actuated end 52, which is a thumb rest, extends from the outer segment 501 so as to be actuated to move the stem portion 50a along the passage 21.
The plunger 50 further includes a head 50b which has a tapered surrounding abutting portion 541 that extends from the retaining protrusion 542 of the inner segment 502 toward the grip segment of the needle seat 30, and a spindle portion 55 which extends upwardly from the surrounding abutting portion 541 along the axis (X) and which terminates at two split halves 552,553 that are spaced apart from each other in a direction transverse to the longitudinal direction with a concave space 551 inbetween. The split halves 552,553 respectively have upper terminal anchoring edges 554,555. Preferably, the spindle portion 55 has an outer diameter which decreases from the surrounding abutting portion 541 toward the split halves 552,553. Moreover, the surrounding abutting portion 541 and the retaining protrusion 542 are configured to be substantially hollow so as to provide greater flexibility.
A deformable surrounding engaging portion 60, preferably made of an elastic material, is retainingly sleeved on the whole retaining protrusion 542 of the inner segment 502 and a portion 5 of the surrounding abutting portion 541 to generate a second friction force. The surrounding engaging portion 60 has upper and lower end faces 64,65 opposite to each other in the longitudinal direction and proximate to and distal from the lower surrounding edge portion 33 of the needle seat 30, respectively, 10 and an outer surrounding surface 63 disposed therebetween. The lower end face 65 is distal from the surrounding flange 51 by a space (S) . The outer surrounding surface 63 sealingly contacts and is slidable relative to the larger-diameter segment 213 of the barrel 20 so as to be moved with the stem portion 50a.
Preferably, the outer surrounding surface 63 is concaved toward the axis (X) to decrease contact area between the outer surrounding surface 63 and the larger-diameter segment 213 so as to facilitate sliding movement of the surrounding engaging portion 60 relative to the larger-diameter segment 213.
With reference to Fig. 5, in use, the plunger 50 is pressed forwardly to push the upper end face 64 of the surrounding engaging portion 60 to abut against a lower edge surface 332 of the lower surrounding edge portion 33 of the needle seat 30. Since the spindle portion 55 is configured to be tapered upwardly and to match with the inner tubular wall surface 324 of the needle seat 30, drug solution in the passage 21 can almost be completely injected via the needle unit 40.
Subsequently, referring to Fig. 6, when the plunger 50 is further moved forward by a third force towards the smaller-diameter segment 214 against the second friction force between the inner segment 502 and the surrounding engaging portion 60, the surrounding engaging portion 60 is deformed by the lower surrounding edge portion 33, thereby decreasing the space (S) and permitting the surrounding abutting portion 541 of the head 50b to move in the concave portion 326 of the needle seat 30 to abut against the second surrounding shoulder portion 329.
Meanwhile, the split halves 552,553 of the spindle portion 55 are pressed by the inner tubular wall surface 324 to move towards each other against a biasing action when the split halves 552 , 553 are moved towards the upper surrounding edge portion 321.
Once the split halves 552,553 are moved beyond the upper surrounding edge portion 321, the upper terminal anchoring edges 554,555 will engage the upper surrounding edge portion 321 to generate a friction force that combines with the friction force between the surrounding abutting portion 541 and the second surrounding shoulder portion 329 to form a fourth friction force that is greater than the first friction force between the retaining protrusion 327 and the retaining groove 223.
After use, referring to Fig. 7, the outer segment 501 of the plunger 50 is pulled backward to be remote from the finger flange 23 so that the needle seat 30, on which the used needle unit 40 is mounted, is retracted into the passage 21 via the upper open end 212 to bring the upper surrounding edge portion 321 to a retracted position. When the surrounding flange 51 abuts against the protruding ring 217, further movement of the plunger 50 is prevented, thereby restraining the surrounding engaging portion 60 from being moved out of the lower open end 211. In this state, the used needle unit 40 can be enclosed in the passage 21 of the barrel 20 for disposal.
Consequently, chances that the user may be accidentally pricked or pierced by the needle 41 are slim. The safety in use and disposal is thus enhanced.
Furthermore, the wing plates 53 at the inner segment 502 have a weakening area 531 disposed proximate to the surrounding flange 51. As such, when the plunger 50 is retracted to push the surrounding flange 51 to abut against the protruding ring 217, the weakening area 531 extends outwardly of the lower open end 211 so as to ease breaking of the stem portion 50a off the plunger 50 at the weakening area 531 for convenient disposal.
Ref erring to Fig . 8 , the second pref erred embodiment of the disposable syringe according to this invention is shown to be similar to the aforesaid embodiment in construction. The differences therebetween reside in that the spindle portion in the aforesaid embodiment is dispensed with. An elastic surrounding engaging portion 60 is retainingly sleeved on the whole retaining protrusion 742 and a portion of the surrounding abutting portion 741. As such, when the surrounding engaging portion 60 is brought by the stem portion 73 of the plunger 70 upwardly to engage and to be depressed by the lower surrounding edge portion 33 of the needle seat 30, the surrounding engaging portion 60 is retained by the lower surrounding edge portion 33, thereby permitting the surrounding abutting portion 741 to be retained in the concave portion 326, as shown in Fig. 9. Hence, the needle seat 30 and the needle unit 40 can be retracted into the passage 21 of the barrel 20 after an injection procedure to permit breaking of the stem portion 73 of the plunger 70 at a weakening area 731 for safe disposal, as shown in Fig. 10.
Referring to Figs . 11 and 12 , the third pref erred embodiment of the disposable syringe according to this invention is shown to be similar to the aforesaid embodiments in construction. The differences therebetween reside in that a tubular needle seat 30 has a duct 31 with a relatively small diameter at the upper segment 323 so as to engage fittingly the needle 41. Thus, the needle hub 42 can be eliminated.
Moreover, a barrel 20 has an outer surrounding wall surface 222 with a sleeved portion 2221 which is disposed proximate to the upper open end 212 to replace the sleeved portion 423 shown in Fig. 2, and which has a plurality of friction ribs 224 formed thereon. Thus, a tip protector 43, which has a plurality of frictional ribs 433 formed on an internal sleeve end 431 thereof, can be sleeved f fittingly on the sleeved portion 2221 for shielding the needle 41.
In the syringe assembly of this embodiment, the number of components is decreased. Similarly, the needle seat 30 and the needle 41 can be retracted into the passage 21 of the barrel 20 after an injection procedure.
Referring to Fig. 13, the fourth preferred embodiment of the disposable syringe with a similar construction of the aforesaid embodiments, is used for an extremely small injection volume, such as 1 ml. Thus, the dimensions of the barrel 20, the needle seat 30, the needle 41, the plunger 70, and the deformable surrounding engaging portion 60 are smaller than those of the aforesaid embodiments.
Referring to Figs. 14 and 15, the fifth and sixth preferred embodiments of the disposable syringe according to this invention are shown to be similar to the third and fourth embodiments in construction, respectively. The differences therebetween reside in that the upper open end 212 has a surrounding edge wall 219 which extends from the smaller-diameter segment 214 of the inner surrounding barrel wall surface 221 of the barrel 20 toward the axis (X) and which confines a through hole 210 that surrounds the axis (X) . As such, the needle 41 can pass through the through hole 210 and outwardly of the upper open end 212. The sixth preferred embodiment shown in Fig. 15 is similar to the fifth preferred embodiment in construction, but is used for an extremely small injection volume, such as 1 ml.
While the present invention has been described in connection with what is considered the most practical and preferred embodiments, it is understood that this invention is not limited to the disclosed embodiments but is intended to cover various arrangements included within the spirit and scope of the broadest interpretations and equivalent arrangements.
Claims (15)
1. A disposable syringe to be used with a needle unit, comprising:
a barrel having an inner surrounding barrel wall surface which surrounds an axis and which confines a passage, said passage having lower and upper open ends which are disposed opposite to each other in a longitudinal direction parallel to the axis; and a plunger including:
a stem portion disposed to be movable in said passage of said barrel, and having inner and outer segments opposite to each other in the longitudinal direction, said outer segment extending outwardly of said lower open end;
and an actuated end extending from said outer segment so as to be actuated to move said stem portion along said passage, wherein said inner surrounding barrel wall surface of said barrel includes a larger-diameter segment and a smaller-diameter segment which are disposed proximate to said lower and upper open ends, respectively, and which cooperatively form a first surrounding shoulder portion therebetween, said smaller-diameter segment including a retaining groove defined therein;
said disposable syringe further comprising:
a tubular needle seat disposed to be insertable into said passage from said lower open end toward said upper open end, and adapted to be fitted with the needle unit, said needle seat including a protruding lower surrounding edge portion which is disposed to abut against said first surrounding shoulder portion, an upper surrounding edge portion disposed opposite to said lower surrounding edge portion in the longitudinal direction, and a surrounding seat wall interposed said lower and upper surrounding edge portions, and having an inner tubular wall surface which surrounds the axis to confine a duct and which has a grip segment, and an outer tubular wall surface which includes a lower segment including a retaining protrusion defined thereon and proximate to said lower surrounding edge portion, said lower segment being configured such that, when said upper surrounding edge portion is forced to extend toward said upper open end after said tubular needle seat is inserted into said passage, said lower segment will be brought to a position of use, where said lower segment engages and is retained at said smaller-diameter segment by virtue of a first friction force generated by retaining engagement of said retaining protrusion in said retaining groove while said protruding lower surrounding edge portion abuts against said first surrounding shoulder portion, said lower segment being further configured such that, when said upper surrounding edge portion is moved against the first friction force toward said lower open end passing said larger-diameter segment, said needle seat will be brought to a retracted position, where said lower segment and said protruding lower surrounding edge portion are remote from said smaller-diameter segment and said first surrounding shoulder portion, respectively; and an upper segment disposed opposite to said lower segment and proximate to said upper surrounding edge portion;
said plunger further including:
a surrounding engaging portion which is disposed to retaining sleeve on said inner segment by virtue of a second friction force, and which is in sealing contact with and which is slidable relative to said larger-diameter segment so as to be moved with said stem portion to the position of use, and a head disposed to extend from said inner segment toward said grip segment of said inner tubular wall surface, and configured such that, when said surrounding engaging portion is brought by said inner segment to engage said lower surrounding edge portion and is depressed by said lower surrounding edge portion by virtue of a third force generated as a consequence of continuing movement of said inner segment towards said smaller-diameter segment, the third force being greater than the second friction force such that said surrounding engaging portion is blocked by said lower surrounding edge portion to thereby permit said head to move towards said grip segment and to be held by virtue of a fourth friction force that is greater than the first friction force while said lower segment remains engaged and unmoved relative to said smaller-diameter segment.
a barrel having an inner surrounding barrel wall surface which surrounds an axis and which confines a passage, said passage having lower and upper open ends which are disposed opposite to each other in a longitudinal direction parallel to the axis; and a plunger including:
a stem portion disposed to be movable in said passage of said barrel, and having inner and outer segments opposite to each other in the longitudinal direction, said outer segment extending outwardly of said lower open end;
and an actuated end extending from said outer segment so as to be actuated to move said stem portion along said passage, wherein said inner surrounding barrel wall surface of said barrel includes a larger-diameter segment and a smaller-diameter segment which are disposed proximate to said lower and upper open ends, respectively, and which cooperatively form a first surrounding shoulder portion therebetween, said smaller-diameter segment including a retaining groove defined therein;
said disposable syringe further comprising:
a tubular needle seat disposed to be insertable into said passage from said lower open end toward said upper open end, and adapted to be fitted with the needle unit, said needle seat including a protruding lower surrounding edge portion which is disposed to abut against said first surrounding shoulder portion, an upper surrounding edge portion disposed opposite to said lower surrounding edge portion in the longitudinal direction, and a surrounding seat wall interposed said lower and upper surrounding edge portions, and having an inner tubular wall surface which surrounds the axis to confine a duct and which has a grip segment, and an outer tubular wall surface which includes a lower segment including a retaining protrusion defined thereon and proximate to said lower surrounding edge portion, said lower segment being configured such that, when said upper surrounding edge portion is forced to extend toward said upper open end after said tubular needle seat is inserted into said passage, said lower segment will be brought to a position of use, where said lower segment engages and is retained at said smaller-diameter segment by virtue of a first friction force generated by retaining engagement of said retaining protrusion in said retaining groove while said protruding lower surrounding edge portion abuts against said first surrounding shoulder portion, said lower segment being further configured such that, when said upper surrounding edge portion is moved against the first friction force toward said lower open end passing said larger-diameter segment, said needle seat will be brought to a retracted position, where said lower segment and said protruding lower surrounding edge portion are remote from said smaller-diameter segment and said first surrounding shoulder portion, respectively; and an upper segment disposed opposite to said lower segment and proximate to said upper surrounding edge portion;
said plunger further including:
a surrounding engaging portion which is disposed to retaining sleeve on said inner segment by virtue of a second friction force, and which is in sealing contact with and which is slidable relative to said larger-diameter segment so as to be moved with said stem portion to the position of use, and a head disposed to extend from said inner segment toward said grip segment of said inner tubular wall surface, and configured such that, when said surrounding engaging portion is brought by said inner segment to engage said lower surrounding edge portion and is depressed by said lower surrounding edge portion by virtue of a third force generated as a consequence of continuing movement of said inner segment towards said smaller-diameter segment, the third force being greater than the second friction force such that said surrounding engaging portion is blocked by said lower surrounding edge portion to thereby permit said head to move towards said grip segment and to be held by virtue of a fourth friction force that is greater than the first friction force while said lower segment remains engaged and unmoved relative to said smaller-diameter segment.
2. The disposable syringe of Claim 1, further characterized in that one of said lower segment and said smaller-diameter segment is formed with a retaining groove, and the other one of said lower segment and said smaller-diameter segment is formed with a retaining protrusion which engages retainingly said retaining groove when said lower segment is brought to the position of use so as to generate the first friction force.
3. The disposable syringe of Claim 1, further characterized in that said grip segment has a concave portion which extends inwardly from said inner tubular wall surface in radial directions relative to the axis to form a second surrounding shoulder portion that is adjacent to said lower surrounding edge portion, said head having a surrounding abutting portion which is configured so as to be insertable into said concave portion and to abut against said second surrounding shoulder portion, thereby generating the fourth friction force to hold said needle seat at the retracted position.
4. The disposable syringe of Claim 3, further characterized in that said head has a spindle portion which extends from said surrounding abutting portion along the axis and which terminates at two split halves that are spaced apart from each other in a direction transverse to the longitudinal direction, said split halves respectively having two upper terminal anchoring edges which are remote from said surrounding abutting portion and which are configured such that said split halves are pressed by said inner tubular wall surface to move towards each other against a biasing action when said split halves are moved towards said upper surrounding edge portion, and such that said upper terminal anchoring edges engage said upper surrounding edge portion once said split halves are moved beyond said upper surrounding edge portion.
5. The disposable syringe of Claim 4, further characterized in that said inner tubular wall surface has a diameter which gradually decreases from said lower surrounding edge portion to said upper surrounding edge portion, said spindle portion having an outer diameter which gradually decreases from said surrounding abutting portion to said split halves.
6. The disposable syringe of Claim 3, further characterized in that said surrounding engaging portion is made of a deformable material, and has upper and lower end faces opposite to each other in the longitudinal direction and proximate to and distal from said lower surrounding edge portion, respectively, and an outer surrounding surface disposed between said upper and lower end faces and concaved toward the axis.
7. The disposable syringe of Claim l, further characterized in that said lower surrounding edge portion has an upper edge surface which abuts against said first surrounding shoulder portion when said lower segment is at the position of use, and a lower edge surface for abutment and depression by said surrounding engaging portion.
8. The disposable syringe of Claim 1, further characterized by a spline member disposed between said smaller-diameter segment and said lower segment to prevent relative rotation therebetween.
9. The disposable syringe of Claim 1, further characterized by a protruding ring which is disposed on and which projects inwardly and radially from said larger-diameter segment adjacent to said lower open end, and a surrounding flange which is disposed to surround said inner segment adjacent to said head and which is engageable with said protruding ring.
10. The disposable syringe of Claim 9, further characterized in that said inner segment has a weakening area which is disposed proximate to said surrounding flange such that when said surrounding flange is brought to engage said protruding ring, said weakening area extends outwardly of said lower open end so as to ease breaking of said stem portion off said plunger at said weakening area.
11. The disposable syringe of Claim 3, further characterized in that said surrounding abutting portion is configured to be substantially hollow for greater flexibility.
12. The disposable syringe of Claim 1, further characterized in that said barrel has an outer surrounding wall surface disposed opposite to said inner surrounding barrel wall surface in radial directions and having a sleeved portion which is disposed proximate to said upper open end, said disposable syringe further comprising a tip protector which has an internal sleeve end configured to be sleeved on said sleeved portion so as to shield a needle of the needle unit .
13. The disposable syringe of Claim 12, further characterized in that each of said sleeved portion and said internal sleeve end has a plurality of friction ribs formed thereon.
14. The disposable syringe of Claim 13, further characterized in that said upper open end has a surrounding edge wall which extends from said smaller-diameter segment of said inner surrounding barrel wall surface toward the axis and which confines a through hole that surrounds the axis and that is adapted for passage of the needle of the needle unit.
15. The disposable syringe of Claim 1, further characterized in that said upper segment and said upper surrounding edge portion extend outwardly of said upper open end when said lower segment is in the position of use, said disposable syringe further comprising a needle hub which is adapted to secure a needle of the needle unit, which is disposed to sleeve over said upper segment, and which has a sleeved portion, and a tip protector which has an internal sleeve end configured to be sleeved on said sleeved portion so as to shield the needle.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2408757 CA2408757C (en) | 2002-10-17 | 2002-10-17 | Disposable syringe |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2408757 CA2408757C (en) | 2002-10-17 | 2002-10-17 | Disposable syringe |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2408757A1 CA2408757A1 (en) | 2004-04-17 |
| CA2408757C true CA2408757C (en) | 2007-02-06 |
Family
ID=32399746
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2408757 Expired - Fee Related CA2408757C (en) | 2002-10-17 | 2002-10-17 | Disposable syringe |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2408757C (en) |
-
2002
- 2002-10-17 CA CA 2408757 patent/CA2408757C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2408757A1 (en) | 2004-04-17 |
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| Date | Code | Title | Description |
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| EEER | Examination request | ||
| MKLA | Lapsed |