Title of Invention

SINGLE USE SAFETY SYRINGE

Abstract

A safety device for a syringe needle which includes a guide: -a slidable member having a first portion that is configured to be said along the guide and positioned relative the guide in a pre-determined position, the first portion including a bracket and a resiliently deformable shaft biased away from a barrel of a syringe; and -a second portion attached to the biased shaft, wherein the second portion has a shielding formation for a needle-point, a part of said formation faciliating the shielding of a point of the needle when the shaft is biased away the barrel of the syringe

Full Text

FORM 2 THE PATENTS ACT, 1970 (39 of 1970) & THE PATENTS RULES, 2003 COMPLETE SPECIFICATION [See section 10, Rule 13] SINGLE USE SAFETY SYRINGE AFRICAN VENTURES AND TECCHNOLOGIES (PTY) LTD, CORPORATION ORGANIZED AND EXISTING UNDER THE LAWS OF SOUTH AFRICA WHOSE ADDRESS IS 57 SABI SAND CRESCENT .MEADOW HEIGHTS, TIMBAVATI STREET.MORELETTA PARK EXTENSION 51, PETORIA, SOUTH AFRICA. THE FOLLOWING SPECIFICATION PARTICULARLY DESCRIBES THE INVENTION AND THE MANNER IN WHICH IT IS TO BE PERFORMED. GRANTED ORIGINAL 28 MAR 2008 28-3-2008 FIELD OF THE INVENTION 2 The present invention lies in the field of safety syringes, particularly those that prevent needle stick injuries and that are rendered permanently non-reusable. BACKGROUND With the ever-increasing risk of acquiring the Human Immunodeficiency Virus and other blood-born infections, a need exists for a reliable, easy-to-use and cost effective safety syringe that minimizes the exposure of the healthcare worker and patient. A multitude of proposals have been made in the field. However these generally exhibit disadvantages such as requiring both hands of the healthcare worker to operate and/or having a high manufacturing cost. The cost of medical care in impoverished third world countries has resulted in the re-use of disposable medical equipment, often without adequate sterilization. In light of the high incidence of HIV and related illnesses in these countries, this situation is unacceptable. Patient education is often not optimal, and the unsophisticated patient is more likely to accept re-used equipment! Available mechanisms to render syringes non-reusable have been found to be expensive and some are even made re-usable by the determined user. THE INVENTION The present invention provides a safety device for a syringe needle which includes, a guide mounted on the barrel of a syringe or being an integral moulded part of the barrel, a slidable member with a first portion configured to be slid along the guide and a second portion having a formation for a needle, that facilitates the shielding of the sharp point within that formation. The guide has proximal and distal ends. The proximal end is defined by a terminal block that prevents the first portion of the slidable member from disengaging from the guide at the proximal end, a bevelled segment that allows for connection with the first portion of the slidable member and a chamfered segment to facilitate the temporary positioning of the first portion before the slidable member is advanced to engage with the needlepoint. The distal end of the guide is defined by a segment of aligned toothed serrations that, when in use, engage with a complementary segment on the first portion of the slidable member and thereby lock the slidable member in a non-retractable position with the needle enclosed within the second portion. The first portion of the slidable member consists of a bracket and a shaft. The bracket is configured to snap-click onto the bevelled segment of the guide The second portion of the slidable member may be in the form of a cup- or cap shaped formation for a needle or an eccentric aperture for said needle with a closed segment for shielding the needle. The first portion of the slidable member can be resiliency deformable and biased e.g. away from the barrel of the syringe, so that when the slidable member is advanced towards the needle, until the cap slips off the end of the needle, since the aperture or formation provided for the needle is angled away from the needlepoint, the point is thereby shielded within the cap. The inventor believes that the safety syringe only needs one hand for rendering the needlepoint safe and thereby allows the healthcare worker to utilise the other hand for patient care and to keep the other hand away from the needlepoint. Another aspect of the invention is a means of making a syringe non-re*usable and consists of a plunger having a first part with one or more followers a second part housing a guide for receiving and guiding the followers. A sealing plug may be attached to the end of the plunger or may form a single unit with the second part of the plunger. The second part of the plunger may in itself comprise two portions- a first portion housing the guide, and a second portion that serves as a means for connecting the sealing plug. The guide can consist of at least two legs with an apex, but can also be Z- or M-shaped. A M-shaped guided guide can include a first, second, third and fourth leg, with a first apex point between the first and second leg, a second apex point between the second and third leg and a third apex point between the third and fourth leg. At the first, second and third apex point a means is provided for to ensure a one-directionai pathway of the followers in the guide. This means may be in the form of compressible moulded protrusions with a stepped incline preventing re-entry into a preceding leg. The first leg of the M-shaped guide receives the follower, as the plunger is advanced in the syringe. The first leg can be used to prepare the syringe to the position needed to draw fluid into the syringe, or it can be used to inject an amount of air into another vial. It is preferable that the follower is assembled within the guide and that the plunger is inserted into the barrel opening before the syringe is used. Once the follower has advanced along the first leg, the first apex of the M-shaped guide is configured to encourage a path towards the second leg of the M-shaped guide. The second leg of the M-shaped guide, guides the follower as the plunger is pulled away from the needle end of the syringe. This action will correspond with the filling of the syringe of medication, body fluids and the like. The second apex is configured to encourage a path towards the third leg of the M-shaped guide. The third leg of the M-shaped guide receives the follower as the plunger is pushed towards the needle end of the syringe. This action corresponds with the administering of the content to the patient or the -depositing of the blood or fluid sample in an appropriate container. The third apex point then encourages a path towards the fourth leg of the M-shaped guide, if an attempt is made to re-use the syringe or to remove the plunger from the barrel of the syringe. The fourth leg of the M-shaped guide receives the follower as the plunger is drawn back from the needle end of the syringe. This fourth leg is in communication with the exterior of the second part of the plunger and thereby allows the follower to slide out of the M-shape guide and thereby disassociates the first part of the plunger from the second part and thus causes the second part and the plunger to remain at the needle end of the syringe. The needle can be pre-manufactured with the syringe and non¬removable. A Z-shaped guide can include a first, second and third leg, with a first apex point between the first and second leg and a second apex point between the" second and third leg. In this instance the syringe would typically be ready for use with the plunger fully inserted into the barrel of the syringe. The first and second apex can have a means for encouraging a one-directional pathway of the followers. This means can be in the form of compressible moulded protrusions with a stepped incline preventing re-entry into a preceding leg. The first leg of the Z-shape, receives the follower as the plunger is pulled away from the needle end of the syringe. The first apex is configured to encourage a path towards the second leg of the Z-shape. The second leg of the Z-shape receives the follower as the plunger is pushed towards the needle end of the syringe. On reaching the second apex point, a path towards the third leg of the Z-shape is encouraged. The third leg of the Z-shape receives the follower as the plunger is drawn back from the needle end of the syringe, and this third leg of the Z-shape is then in communication with the exterior of the plunger and in so doing allows the follower to slide out of the Z-shape guide and thereby disassociates the first part of the plunger from the second part of the plunger, causing the second part to remain at the needle end of the syringe. The needle can be pre-manufactured with the syringe and non¬removable. A V-shaped guide and can include a first and second leg, with an apex point between the first and second leg. A means for encouraging a one-directional pathway of the followers can be located within the apex and can be in the form of compressible moulded protrusions with a stepped incline preventing re-entry into a preceding leg. The first leg of the V-shape, receives the follower as the plunger is pushed towards the needle end of the syringe. Upon reaching the apex, the follower can be encouraged to follow a path towards the second leg of the V-shape. The second leg of the v-shape receives the follower as the plunger is pulled away from the needle end of the syringe. This second leg of the V-shape is in communication with the exterior of the plunger and in so doing allows the follower to slide out of the V-shape guide and thereby disassociates the first part of the plunger from the second part of the plunger, causing the second part to remain at the needle end of the syringe. The non-reusable syringe with a V-shaped guide can be a pre-filled syringe and/or the needle can be a pre-manufactured part of the syringe. THE DRAWINGS . The invention is more fully described by way of a non-limiting example, with reference to the drawings, in which :- Figure 1 is a drawing of the safety device and a syringe. Figure 2 is an enlarged view of the guide. Figure 3 and Figure 4 are enlarged views of the slidable member of the safety device. Figures 5 and 6 are enlarged views of the formation for the needle Figure 7[a] and [bj show the safety syringe in use. Figure 8 is a drawing of the plunger for a non-reusable syringe. Figure 9 is an enlarged view of the guide. Figure 10 is a drawing of the protrusions within the apex points. Figures 11 [a] to [e] show the syringe in use Figure 12 shows a combined non-reusable safety stringe. THE PREFERRED EMBODIMENTS As shown in the Figures 1 to7, the safety device 10 for a syringe needle 12 includes, a guide 14 mounted on the barrel 16 of a syringe 18 or being an integral moulded part of the barrel 16 and a slidable member 20 with a first portion 22 configured to be slid along the guide 14 and a second portion 24 having a formation 26 for a needle 12, that facilitates the shielding of the sharp point 13 within that formation 26. The guide 14 has proximal and distal ends. The proximal end is defined by a terminal block 28 that prevents the first portion 22 of the slidable member from disengaging from the guide 14 at the proximal end, a bevelled segment 30 that allows for connection with the first portion 22 of the slidable member and a chamfered segment 32 to facilitate the temporary positioning of the first portion 22 before the slidable member 20 is advanced to engage with the needlepoint 13.The distal end of the guide 14 is defined by a segment of aligned toothed serrations 34 that, when in use, engage with a complementary segment 36 on the first portion 22 of the slidable member 20 and thereby lock the slidable member 20 in a non-retractable position with the needlepoint 13 shielded by the formation for the needle 26. The first portion 22 of the slidable member 20 consists of a bracket 23 and a shaft 25. The bracket 23 is configured to snap-click onto the bevelled segment 30 of the guide 14. The second portion 24 of the slidable member 20 has a formation 26 for a needlepoint 13 in the form of a cup shape 38 or a cap 40The formation 26 has an eccentric aperture 42 for said needlepoint 13 with a closed segment 44 for shielding the needlepoint 13. The needle 12 penetrates the aperture 42 of the formation 26, thereby causing the formation 26 to rest at the base of the needle 15 when the bracket 23 of the slidable member 20 is positioned on the chamfered segment 32. The first portion 22 of the slidable member 20 can be resiliently deformable and biased away from the barrel 16 of the syringe 18 so that when the slidable member 20 is advanced towards the needle 12, until the cap 40 slips off the end of the needlepoint 13, since the aperture 42 or formation 26 provided for the needle 12 is angled away from the needlepoint 13, the point is thereby shielded by the cap 40 (See Fig.4) The slidable member of the safety syringe enables only one hand to be used for rendering the needlepoint safe and thereby allows the healthcare worker to • utilise the other hand for patient care and to keep the other hand away from the needlepoint. According to another aspect of the invention, as shown in Figures 8 to 11, a non-reusable syringe 50 that has a plunger 52, having a first part 54 with one or more followers 56, in the form of nipples on flexible flaps 57 and a second part 58 housing a guide 60 for receiving and guiding the followers 56. A sealing plug 62 may be attached to the end of the plunger 52 or may form a single unit with the second part 58 of the plunger 52. The second part 58 of the piunger 52 may in itself comprise two portions- a first portion 64 housing the guide 60, and a second portion 66 that serves as a means for connecting the sealing plug 62. The guide 60 can consist of at least two legs with an apex (viz. V-shaped), but can also be Z- or M-shaped. A M-shaped guide 68 can include a first 70, second 72, third 74 and fourth 76 leg, with a first apex point 78 between the first 70 and second 72 leg, a second apex point 80 between the second 72 and third 74 leg and a third apex point 82 between the third 74 and fourth 76 leg. At the first 78, second 80 and third 82 apex point a means 84 is provided for to ensure a one-directional pathway of the followers in the guide. This means may be in the form of compressible moulded protrusions 86 with a stepped incline preventing re-entry into a preceding leg. The first leg 70 of the M-shape receives the follower 56, as the plunger 52 is advanced in the syringe 50. The first leg 70 can be used to prepare the syringe 50 to the position needed to draw fluid into the syringe 50, or it can be used to inject an amount of air into another vial. It is preferable that the follower 56 is assembled within the guide 60 and that the plunger 52 is inserted into the barrel opening 53 before the syringe 50 is used. Once the follower 56 has advanced along the first leg 70, the first apex 78 of the M-shaped guide 68 is configured to encourage a path towards the second leg 72 of the M-shaped guide 68, The second leg 72 of the M-shaped guide 68, guides the follower 56 as the plunger 52 is pulled away from the needle end 51 of the syringe 50. This action will correspond with the filling of the syringe of medication, body fluids and the like. The second apex 80 is configured to encourage a path towards the third leg 74 of the M-shaped guide 68. The third leg 74 of the M-shaped guide 68 receives the follower 56 as the plunger 52 is pushed towards the needle end 51 of the syringe 50. This action corresponds with the administering of the content to the patient or the depositing of the blood or fluid sample in an appropriate container. The third apex point 82 then encourages a path towards the fourth leg 76 of the M-shaped guide 68, if an attempt is made to re-use the syringe 50 or to remove the plunger 52 from the barrel of the syringe 50. The fourth leg 76 of the M-shaped guide 68 receives the follower 56 as the plunger 52 is drawn back from the needle end 51 of the syringe 50. This fourth leg 76 is in communication with the exterior 88 of the second part 58 of the plunger 52 and thereby allows the follower 56 to slide out of the M-shaped guide 68 and thereby disassociates the first part 54 of the plunger 52 from the second part 58 and thus causes the second part 58 and the plunger 52 to remain at the needle end 51 of the syringe 50. The needle can be a pre-manufactured part of the syringe REFERENCE NUMERALS 10-Safety device 12-Needle 13-Needlepoint 14-Guide 15 - Base of the needle 16-Barrel 18 - Syringe 20 - Slidable member 22 - First portion of the slidable member 23 - Bracket 24 - Second portion of the slidable member 25-Shaft 26 - Formation 28 - Terminal block 30 - Bevelled segment 32 - Chamfered segment 34 - Serrations on guide 36 - Serrations on slidable member 38 - Cup-shaped formation 40 - Cap-shaped formation 42 - Eccentric aperture 44 - Closed segment 50 - Non-reusable syringe 51 - Needle end of the syringe 52 - Plunger 53 - Barrel opening 54 - First part of the plunger 56 - Followers 57 - Flexible flaps with nipples 58 - Second part of the plunger 60 - Guide 62 - Sealing plug 64 - First portion of second part 66 - Second portion of second part 68 - M-shaped guide 70 - First leg 72 - Second leg 74 - Third Leg 76 - Fourth leg 78 - First apex 80 - Second apex 82 - Third apex 84 - One directional flow means 86 - Protrusions 88 -Communication point WE CLAIM: 1. A single use safety syringe having a plunger, said syringe includes a safety device for the syringe needle, which comprises; a guide; a slidable member having a first portion that is configured to be slid along the guide; said first portion including a bracket and a resiliency deformable shaft biased away from a barrel of the syringe; and a second portion having a formation for a needle of the syringe in the form of a cap that facilitates the shielding of the needle point. 2. A single use safety syringe as claimed in claim 1, wherein the second portion of the slidable member consists of an eccentric aperture in the cap and a closed segment. 3. A single use safety syringe as claimed in claim 2, wherein the resiliently deformable shaft of the first portion causes the aperture to be biased away from the needle point so that the closed segment comes to rest over the needle point. 4. A single use safety syringe as claimed in any one of claims 1 to 3, wherein the guide is an integrally moulded part of the barrel of the syringe. 5. A single use safety syringe as claimed in any one of claims 1 to 3, wherein the guide is removably attached to at least a part of the barrel of the syringe. 6. A single use safety syringe as claimed in any one of claims 1 to 5, wherein the guide has proximal and distal ends, wherein said proximal end is defined by a terminal block that prevents the slidable member from disengaging from the guide at the proximal end, a beveled segment for receiving the first portion of the slidable member and a chamfered segment to facilitate the temporary positioning of the slidable portion before engagement with the needle point. 7. A single use safety syringe as claimed in any one of claims 1 to 6, wherein the distal end of the guide is defined by a segment of distally aligned toothed serrations that when in use engage with a corresponding segment of the first portion of the slidable member and thereby lock the slidable member in a non-retractable position. 8. A single use safety syringe as claimed in any one of claims 1 to 7, wherein the bracket of the first portion is configured to snap click onto the bevelled segment of the guide. 9. A single use safety syringe as claimed in any one of claims 1 to 8, wherein the bracket of the slidable member has an inner lip complementarily serrated to lock with the toothed serrations on the guide distally and in so doing when in use to prevent retraction of the slidable member proximally. 10. A single use safety syringe as claimed in any one of claims 1 to 9, which includes; a plunger having a first part with one or more followers; a second part housing an M-shaped guide whereby the followers on the first part are guided in a predetermined pathway, said guide including; a first, second, third and fourth leg, with a first apex point between the first and second legs, a second apex point between the second and third legs and a third apex point between the third and fourth legs, including a means encouraging a one directional pathway of the followers from the first leg to the second, from the second leg to the third leg, from the third leg to the fourth leg and thence to slide out of the fourth leg thereby to disassociate the first part of the plunger from the second part of the plunger. 11. A single use safety syringe as claimed in claim 10, that includes a sealing plug attached to the end of the plunger. 12. A single use safety syringe as claimed in claim 11, wherein the second part of the plunger comprises two members, the first housing the guide and the second adapted to connect with the sealing plug. 13. A single use safety syringe as claimed in any one of claims 9 to 12, wherein said means for encouraging a one directional pathway is in the form of compressible moulded protrusions with a stepped incline preventing re-entry into a preceding leg. 14. A single use safety syringe substantially as herein described and illustrated. For AFRICAN VENTURES AND TECHNOLOGIES (PTY) LTD. By their Agent (MANISH SAURASTRI) KRISHNA & SAURASTRI

Documents:

176-mumnp-2004-abstract(28-3-2008).doc

176-mumnp-2004-abstract(28-3-2008).pdf

176-mumnp-2004-assigment(26-2-2004).pdf

176-mumnp-2004-cancelled pages(28-3-2008).pdf

176-mumnp-2004-claims(granted)-(28-3-2008).doc

176-mumnp-2004-claims(granted)-(28-3-2008).pdf

176-mumnp-2004-correspondence(28-3-2008).pdf

176-mumnp-2004-correspondence(ipo)-(10-4-2008).pdf

176-mumnp-2004-drawing(28-3-2008).pdf

176-mumnp-2004-form 1(12-3-2008).pdf

176-mumnp-2004-form 1(28-3-2008).pdf

176-mumnp-2004-form 13(12-3-2008).pdf

176-mumnp-2004-form 18(10-2-2006).pdf

176-mumnp-2004-form 1a(12-3-2004).pdf

176-mumnp-2004-form 1a(13-7-2004).pdf

176-mumnp-2004-form 1a(15-4-2004).pdf

176-mumnp-2004-form 2(granted)-(28-3-2008).doc

176-mumnp-2004-form 2(granted)-(28-3-2008).pdf

176-mumnp-2004-form 3(13-7-2004).pdf

176-mumnp-2004-form 3(24-4-2004).pdf

176-mumnp-2004-form 3(28-9-2007).pdf

176-mumnp-2004-form 5(12-3-2004).pdf

176-mumnp-2004-form 5(13-7-2004).pdf

176-mumnp-2004-form 6(15-4-2004).pdf

176-mumnp-2004-form-pct-isa-210(12-3-2004).pdf

176-mumnp-2004-petition under rule 137(1-10-2007).pdf

176-mumnp-2004-petition under rule 138(1-10-2007).pdf

176-mumnp-2004-power of attorney(15-4-2004).pdf

176-mumnp-2004-power of attorney(5-4-2004).pdf

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