CA2156814A1 - Plungerless syringe - Google Patents
Plungerless syringeInfo
- Publication number
- CA2156814A1 CA2156814A1 CA002156814A CA2156814A CA2156814A1 CA 2156814 A1 CA2156814 A1 CA 2156814A1 CA 002156814 A CA002156814 A CA 002156814A CA 2156814 A CA2156814 A CA 2156814A CA 2156814 A1 CA2156814 A1 CA 2156814A1
- Authority
- CA
- Canada
- Prior art keywords
- fluid
- bellows
- cannula
- internal chamber
- passageway
- 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.)
- Abandoned
Links
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
- A61M5/28—Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle
- A61M5/281—Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle using emptying means to expel or eject media, e.g. pistons, deformation of the ampoule, or telescoping of the ampoule
- A61M5/282—Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle using emptying means to expel or eject media, e.g. pistons, deformation of the ampoule, or telescoping of the ampoule by compression of deformable ampoule or carpule wall
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C69/00—Combinations of shaping techniques not provided for in a single one of main groups B29C39/00 - B29C67/00, e.g. associations of moulding and joining techniques; Apparatus therefore
- B29C69/004—Combinations of shaping techniques not provided for in a single one of main groups B29C39/00 - B29C67/00, e.g. associations of moulding and joining techniques; Apparatus therefore making articles by joining parts moulded in separate cavities, said parts being in said separate cavities during said joining
-
- 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
- A61M2005/3117—Means preventing contamination of the medicament compartment of a syringe
- A61M2005/3118—Means preventing contamination of the medicament compartment of a syringe via the distal end of a syringe, i.e. syringe end for mounting a needle cannula
-
- 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
- A61M2005/3117—Means preventing contamination of the medicament compartment of a syringe
- A61M2005/3118—Means preventing contamination of the medicament compartment of a syringe via the distal end of a syringe, i.e. syringe end for mounting a needle cannula
- A61M2005/312—Means preventing contamination of the medicament compartment of a syringe via the distal end of a syringe, i.e. syringe end for mounting a needle cannula comprising sealing means, e.g. severable caps, to be removed prior to injection by, e.g. tearing or twisting
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/753—Medical equipment; Accessories therefor
- B29L2031/7544—Injection needles, syringes
Abstract
Plungerless syringe including bellows and cannula portions and a removable tab connected to the cannula tip providing head space for receiving air in the fluid contained in the syringe. Upon removal of the tab, the syringe is filled with substantially bubbleless fluid eliminating risk of an air embolism upon fluid injection as through a needle connected to the syringe. The bellows portions is partially collapsed to expel a portion of the fluid to purge air from fluid delivery devices connected to the syringe such as a needle or catheter and the bellows is further collapsed to flush the remaining fluid from the syringe through the fluid delivery device.
Description
2 Background of the Invention 3 Field of the Invention 4 This invention relates generally to a plungerless syringe and more particularly relates to a plungerless syringe for expelling a 6 fluid in a substantially bubbleless manner thereby substantially 7 eliminating the threat of an air-embolism.
8 Description of the Prior Art --9 Syringes are well known to the art which include a substantially transparent plastic cylindrical tube providing a ll fluid receiving chamber, a plastic plunger mounted slidably in one 12 end of the tube and a metal needle mounted to the other end of the 13 tube. The plunger is withdrawn to create a vacuum and draw fluid 14 into the chamber after which the plunger is forced into the chamber to expel or eject the fluid through the needle. Typically, the 16 plunger and cylindrical member are disposable, but the metal needle 17 typically is reusable and must be removed from the tube for 18 resterilization prior to reuse. Removal of the needle is well l9 known for the possibility of the user being pricked or stuck by the needle with the highly undesirable attendant possibility of 21 infectious disease transmission.
22 Plungerless syringes are known to the art, such as for example 23 the plungerless syringe disclosed in U.S. Patent No. 5,102,398, 24 entitled PLUNGERLESS SYRINGE, and patented April 7, 1992, Barry L.
Farris inventor. This plungerless syringe is disclosed as 26 providing substantially bubbleless fluid ejection or expulsion by 27 the employment of an air chamber attached to the bellows portion of 2 1 S 6 8 1 ~
:
1 the syringe and which air chamber is taught as being for entrapping 2 air contained in the fluid.
3 As further known to those in the art, the plunger of the prior 4 art plunger syringe, noted above, is initially partially depressed to expel some fluid from the syringe so as to purge air from the 6 adapter or fluid delivery device, such as a needle or catheter, to 7 which the syringe is connected thereby reducing, or substantially 8 eliminating, the possibility of the injection of air into a 9 person's blood stream with the attendant possible air embolism.
The construction of the typical prior art plungerless syringe is 11 such that it does not lend itself to two distinct stages of fluid 12 expulsion including a first stage for expelling a portion of the 13 fluid in the syringe to purge air from the delivery system and a 14 second stage for expelling the remaining fluid contained in the syringe.
16 Accordingly, there exists a need for a plungerless syringe 17 providing for two stages of collapse, an initial or purge stage 18 where air contained in the fluid delivery device to which the 19 syringe is attached is purged, and a second flush stage where the remaining fluid in the syringe is expelled.
21 The prior art plunger syringe, noted above, is also used to 22 determine whether the needle has been properly inserted into a 23 blood vessel of a patient. This is accomplished by partially 24 depressing the plunger to expel a portion of the fluid contained in the syringe after which the plunger is withdrawn to reflux the 26 previously expelled fluid and to withdraw a blood sample into the , . ' 2ls68ll 1 transparent syringe which provides a visible determination that the 2 tip of the needle is in fact in a blood vessel. The plungerless 3 syringes known to the prior art do not include any structure 4 permitting such fluid reflux and blood sample withdrawal and hence cannot be used to determine if the needle tip is properly inserted 6 into a blood vessel.
7 Accordingly, there exists a need for a plungerless syringe 8 provided with structure permitting the reflux of previously 9 expelled fluid and a blood sample to determine whether the tip of the needle attached to the plungerless syringe is properly inserted 11 into a blood vessel.
12 Still further, the typical prior art plunger syringe is 13 relatively expensive to manufacture because it must be manufactured 14 in several steps and assembled and frequently lubrication is required.
16 Accordingly, there exists a need in the art for a plungerless 17 syringe which is relatively inexpensive to manufacture, contains no 18 moving parts making the plungerless syringe suitable for radiation 19 and sterilization.
Summary of the Invention 21 It is the object of the present invention to satisfy the 22 foregoing needs in the art.
23 A plungerless syringe satisfying the foregoing needs and 24 embodying the present invention may include cannula and bellows portions, the bellows portion providing a bellows chamber for 26 receiving fluid which is expelled through a passageway formed in 2l~c8l ~
1 the cannula upon the bellows portion being collapsed. The bellows 2 portion may be provided with a configuration causing the bellows 3 portion to collapse by inversion instead of compression. A tab may 4 be provided at the outer end of the cannula portion which provides a chamber permitting the bellows chamber to be over-filled and 6 which provides a head space for receiving air contained in the 7 fluid which head space is isolated from the bellows chamber. The 8 bellows portion may include a first bellows portion providing a 9 purge stage which upon being collapsed expels a portion of the fluid contained in the bellows chamber to purge air from fluid 11 delivery apparatus, such as a needle, catheter or adapter, 12 connected to the cannula portion; the bellows portion may include 13 a second bellows portion providing a flush stage which upon being 14 collapsed expels the remaining fluid contained in the bellows chamber. The rearward portion of the bellows portion may include 16 a push-button member for being pulled rearwardly to reextend the 17 first bellows portion after its collapse in the purge stage to re-18 draw or reflux into the bellows chamber fluid previously expelled 19 during the purge stage to test whether the tip of a needle attached to the syringe is inserted into a blood vessel. Additionally, the 21 bellows portion may include mechanical snap members which retain 22 the bellows portion fully collapsed stage to prevent unintentional 23 reflux of previously expelled fluid.
24 Description of the Drawings FIG. 1 is a side view of a plungerless syringe embodying the 26 present invention;
21S~g 1-1 `
" -1 FIG. 2 is a side view showing the plungerless syringe of FIG.
2 1 rotated 90;
3 FIG. 3 shows the tab portion removed from the bellows and 4 cannula portions of the plungerless syringe;
S FIG. 4 is a diagrammatical view illustrating the manner in 6 which the plungerless syringe of the present invention is held by 7 a user to collapse of the bellows portion of the syringe to expel 8 or inject fluid into a fluid delivery device such as a needle;
9 FIG. 5 is a vertical cross-sectional view of a mold illustrating the forming of a portion of the plungerless syringe;
11 FIG. 6 is a vertical cross-sectional view illustrating the 12 filling of a portion of the plungerless syringe;
13 FIG. 7 is a vertical cross-sectional view of a mold 14 illustrating the forming of a second portion of the plungerless syringe;
16 FIG. 8 is a vertical cross-sectional view illustrating sealing 17 together of the previously formed two portions of the plungerless 18 syringe;
19 FIG. 9 is a side view of the plungerless syringe of the present invention with the tab portion removed in preparation for 21 fluid expulsion or injection;
22 FIG. 10 illustrates the partial collapse of the bellows in the 23 fluid purge stage;
24 FIG. 11 illustrates the further collapse of the bellows in the fluid flush stage;
~1S681,~
1 FIG. 12 illustrates the mechanical snap-fit for maintaining 2 the bellows fully collapsed to permit unintentional fluid reflux;
3 FIG. 13 is a side view of an alternate embodiment of a 4 plungerless syringe embodying the present invention;
FIG. 14 is a side view of the alternate embodiment of the 6 plungerless syringe of FIG. 13 with the tab portion removed in 7 preparation for fluid expulsion or injection;
8 FIG. 15 illustrates the partial collapse of the bellows in the 9 fluid purge stage;
FIG. 16 illustrates a further collapse of the bellows in the 11 fluid flush stage; and 12 FIG. 17 illustrates the position of the bellows in the final 13 collapse stage.
14 Description of the Preferred Embodiment Referring to the drawings and in particuiar to FIGS. 1-3, a 16 plungerless syringe embodying the present invention is shown and 17 indicated by general numerical designation 10; the plungerless 18 syringe is particularly useful for expelling or injecting fluids 19 such as a saline solution, drugs or other fluids typically injected by a syringe into a needle or catheter. The syringe 10 includes a 21 rearward hollow, collapsible, bellows portion indicated by general 22 numerical designation 12, a forward cannula portion 14, a generally 23 semi-spherical dome portion 16 intermediate the bellows portion 12 24 and the cannula portion 14 for substantially receiving the bellows portion upon being collapsed and decreasing in diameter toward the 26 cannula portion, a removable or break-away tab 18 initially secured '. ` 2ls68lq 1 or sealed to the outer tip 19 of the cannula portion 14 and a 2 rearward disk-like or push-button portion 20. The bellows portion 3 12 provides an internal or bellows chamber 22 for receiving fluid 4 to be expelled or in~ected and the cannula portion 14 includes a passageway 24 in fluid communication with the internal chamber 22 6 and through which passageway fluid contained in the chamber is 7 expelled upon the bellows portion 12 being collapsed. The bellows 8 portion 12 includes a first or rearward bellows portion 26 and a 9 second or forward bellows portion 28 and is made of a suitable substantially transparent flexible plastic material described in 11 detail below. The tab 18 provides an over-fill chamber 30 in fluid 12 communication with the cannula passageway 24 and the internal 13 bellows chamber 22 an d which over-fill chamber 30 permits the over-14 filling of the internal bellows chamber 22 and the cannula lS passageway 24 with fluid in the manufacture of the syringe 10 and 16 isolates the head space inherent in any fluid filling operation to 17 the over-fill chamber 30. As will be described in detail below, 18 this isolation of the head space is particularly beneficial in the 19 substantial elimination of the risk of an air embolism because it eliminates head space in the bellows chamber 22 and the cannula 21 passageway 24 which head space is inherent in any fluid filling 22 operation such as when the plungerless syringe is filled with 23 fluid. Thus, it will be understood, when the tab 18 is removed 24 from the cannula portion 14 by being pulled away as indicated by the arrow 31 and twisted as indicated by the arrow 32 in FIG. 3, 26 the tab portion is removed from the cannula portion and the bellows ~' 21~68~
1 chamber 22 and cannula passageway 24 are fluid-filled and ready for 2 use.
3 The cannula tip 19 is formed in the shape of a male luer 4 connector so as to be compatible with a female luer connector typically provided at the hub of a needle or catheter.
6 Referring to FIG. 4, upon the tab 18 being removed as shown in 7 FIG. 3 and described above, the user grasps or holds the bellows 8 portion 12 by placing the index and middle finger around the dome 9 portion 16 and by placing the thumb on the push-button 20. The cannula tip 19 may be previously inserted into the hub portion 33 11 of the needle 34 and the user's thumb is pressed inwardly to apply 12 inwardly acting force indicated by the arrow 35 in FIG. 4 to 13 compress the bellows portion 12 and expel fluid from the syringe 14 into and through the needle 34.
Referring now to FIGS. 5-8 and first to FIG. 5, the 16 plungerless syringe 10 of the present invention may be manufactured 17 in three stages from substantially transparent polyethylene, 18 polypropylene, or blends thereof, or other flexible resin, to make 19 the syringe 10 substantially transparent permitting the user to observe fluid within the bellows chamber 22, the cannula passageway 21 24 and the over-fill chamber 30; such transparency also permits the 22 user to observe the intentional reflux of fluid into the syringe 23 and the withdrawing of blood from a blood vessel determining that 24 the tip of the needle connected to the syringe is properly inserted into a blood vessel. A first stage of manufacture is illustrated 26 in FIG. 5 wherein the bellows portions 12, cannula portion 14, , ' 21~81~
1 push-button portion 20 and a portion 18' of the removable tab 18 2 are formed from the noted plastic materials in a suitable mold 40 3 such as, for example, by a suitable blow molding operation. It 4 will be particularly noted that the tab portion 18' includes an inner portion 42 which is formed integrally with the cannula tip 19 6 thereby initially attaching or mounting the tab portion 18 to the 7 cannula tip 19. It will be understood that the tab portion 42 and 8 the cannula tip 19 are formed integrally in a relatively thin 9 circular ring-like portion, or frangible edge, which may be readily broken to remove the tab 18 from the cannula tip 19 as shown in 11 FIG. 3 and described above.
12 After the first manufacturing stage illustrated in FIG. 5, 13 suitable filling apparatus, not shown except for a filling tube 44, 14 is placed over the mold 40 and the internal bellows chamber 22, the cannula passageway 24, and a portion 30' of the over-fill chamber 16 30 (FIGS. 1-3) are filled with a suitable injectable fluid 46 of 17 the type noted above. It will be noted particularly that the top 18 or fill line of the fluid 46 resides above the cannula tip 19 and 19 resides in the portion 30' of the over-fill chamber 30. Thereafter the fluid filling apparatus is removed.
21 The upper portion 18" of the tab 18 (FIGS. 1-3) may be 22 suitably formed from the noted plastic materials such as by blow 23 molding in a suitable mold 48. The tab portion 18" is formed to 24 include a portion 30" of the over-fill chamber 30 (FIGS. 1-3).
Thereafter, the molds 48 and 40 are brought into engagement as 26 shown in FIG. 8 and the portions 18' and 18" of the tab 18 are ' ' 21~6814 -1 integrated or sealed together with suitable heat and pressure, or 2 by sonic welding, as known to the art for joining separate plastic 3 parts.
4 Referring now to FIGS. 9-12 and in detail to the operation of the plungerless syringe 10 of the present invention, it will be 6 assumed that the tab 18 has been broken away or removed from the 7 cannula tip 19 as shown in FIG. 3 and described above and that the 8 cannula tip 19 has been inserted, for example, into the hub portion 9 33 of the needle 34 shown in FIG. 4; the needle 34 is not shown in FIGS. 5-12 for convenience of illustration. The syringe 10 will be 11 grasped or held by the user as shown in FIG. 4 and inwardly acting 12 force 35 will be applied to the push-button portion 20 as shown in 13 FIG. 10 to collapse the rearward or first bellows portion 26 and 14 expel a portion of the fluid contained in the internal chamber 22 through the cannula passageway 24 and the needle 34 (FIG. 4).
16 Collapse of the rearward bellows portion 28 provides the purge 17 stage noted above and expels air present in the needle 34 or other 18 fluid delivery device which may be attached to the cannula tip 19.
19 After the purge stage, the tab portion 20 may be grasped by the fingers of the other hand of the user (not shown) to pull the tab 21 portion 20 outwardly or rearwardly as indicated by the arrow 50 in 22 FIG. 10, to re-expand or uncollapse the first bellows portion 26 23 into the uncollapsed position shown in FIG. 9 to reflux or aspirate 24 the fluid expelled in the purge stage and to draw into at least the cannula passageway 24 a sample of blood to determine if the tip of 26 the needle is properly inserted into a blood vessel. Accordingly, _ 10--21~G81 i -1 it will be understood that the tab 20 is also an aspiration tab and 2 that the re-expansion of the first bellows portion 26 is an 3 aspiration stage.
4 Thereafter, the inwardly directed force 35 is applied again to the tab 20 as illustrated in FIG. 11 to re-collapse the first 6 bellows portion 26 and to collapse the second bellows portion 28 in 7 the flush stage to expel the fluid contained in the chamber 22 8 through the cannula passageway 24 and through the needle 34 (FIG.
9 4).
Referring again to FIG. 9, it will be noted that the tab 11 portion 20 is provided with a diameter D1 and that the rearward 12 portion of the dome portion 16 provided with a diameter D2. The 13 diameter D1 is larger than the diameter D2 and in an embodiment of 14 the plungerless syringe of the present invention the diameter D1 is 0.458 inch and the diameter D2 is 0.418 inch. Accordingly, upon 16 continued application of the force 35 after collapse of the bellows 17 portion 12, FIG. 12, the disk-like or push-button portion 20 is 18 forced and wedged into the dome portion 16 to maintain the bellows 19 portion 12 collapsed, and thereby prevent unintentional reflux of previously expelled fluid into the syringe 10; it will be noted 21 from FIG. 12 that upon collapse the bellows portion 12 is 22 substantially contained in the dome portion 16.
23 - Referring again to FIG. 2, it will be noted that the forward 24 bellows portion 28 is defined by a wall having a thickness Tl and that the rearward bellows portion 26 is defined by a wall having a 26 thickness T2 and it will be understood that the thickness T2 is ,~ . 21S6~14 1 less than the thickness T1. This difference in wall thickness 2 facilitates collapse of the bellows portion 12 by inversion, 3 instead of compression, as shown particularly in FIG. 12. It has 4 been discovered that collapse of the bellows portion 12 by inversion, instead of compression, is highly desirable because it 6 reduces the possibility of unintentional fluid reflux subsequent to 7 complete collapse of the bellows portion 12. Such inadvertent 8 reflux is undesirable, since it may result in reduced fluid 9 delivery efficiency and can undesirably draw blood into the needle and syringe after total bellows collapse or undesirably draw 11 previously expelled fluid and blood into the fluid delivery device, 12 such as a needle or catheter, connected to the syringe, and such 13 inadvertent reflux can create a vacuum in the needle or other fluid 14 delivery intravenous access device, such as a catheter, which may result in blood reflux into the catheter. Reflux is undesirable 16 because it may result in clot formation within the catheter line.
17 It will be still further understood that the bellows portion 18 12 of the plungerless syringe 10 of the present invention may be 19 fully collapsed in a single step into the position shown in FIG. 12 without the sequential performance of the purge stage and then the 21 flush stage and without the performance of the aspiration step 22 noted above.
23 Referring now to FIGS. 13-17, an alternate embodiment plunger 24 syringe embodying the present invention is shown and indicated by general numerical designation lOA. It will be generally understood 26 that the plungerless syringe lOA is substantially similar to the 21~8~
1 earlier embodiment plungerless syringe 10 and performs 2 substantially the same function in substantially the same way 3 except that plungerless syringe lOA collapses, not by inversion, 4 but instead by compression, does not include the dome portion 16 and the wall thickness of the bellows portion 28A is substantially 6 uniform and does not vary in thickness as does the wall thickness 7 of the bellows portion 28 of embodiment 10. Accordingly, for 8 convenience of presentation and understanding, structural elements 9 comprising plungerless syringe lOA which are the same as the structural elements in plungerless syringe 10 are given the same 11 numerical designations and have the same function.
12 The bellows portion 12A includes a first or rearward portion 13 26A and a second or forward bellows portion 28A and is made of a 14 suitable substantially transparent flexible plastic material as described above for the construction of the bellows 12.
16 Referring to FIGS. 14-17, the rearward or first bellows 17 portion 26A collapses by compression upon the application of the 18 force 35 to the push-button 20 and, as with the first bellows 19 portion 26 of embodiment 10, such collapse expels a portion of the fluid contained in the internal chamber 22A provided by the first 21 and second bellows portions for the same purpose as described 22 above. Afterwards, as explained above, the push-button 20 may be 23 pulled rearwardly by the force 50 shown in FIG. 15 to reflux a 24 portion of the previously expelled fluid as described above and for the same reason. A further application of the force 35, FIGS. 16 26 and 17, expels the balance of the fluid contained in the chamber . ' 21~81~
1 22A and the bellows portion 28A, including first and second bellows 2 portions, collapses by compression into the final expulsion 3 position shown in FIG. 17.
4 It will be further understood that the plungerless syringe embodiment lOA may be made in the same manner as illustrated above 6 for embodiment 10 and as described above and illustrated in FIGS.
7 5-8.
8 Significantly, it will be understood that the removable or 9 break-away tab 18 of embodiment lOA performs the same over-fill and head space isolation function as the correspondingly numbered tab-11 portion 18 of FIGS. 1-3.
12 Referring again to FIGS. 1-3 and 13, it will be noted that the13 tab 18 is relatively large in size and flange-like in shape and the14 size of the tab 18 discourages touch contamination of the tip 19 ofthe cannula 14 upon the tab 18 being removed as shown in FIGS. 3 16 and 14. The bulb shape of the over-fill tab chamber 30 also 17 discourages touch contamination by distancing the fingers from the 18 luer tip.
19 It will be still further understood that while it is possible for the tab 18 to be removed from the tip of the cannula 14 with 21 the plungerless syringe oriented in a horizontal position wherein, 22 of course, the head space could migrate to the bellows portion 22, 23 this is highly unlikely since the loss of fluid from the syringe 24 would be obvious to a user and a user will naturally or normally orient the plungerless syringes 10 and lOA in the vertical position 26 with tab 18 extending upwardly and will do so through the natural t $~81 1 1 inclination of a person opening a fluid filled container to open 2 the container in the vertical position to prevent fluid spillage.
3 Thus, upon the plungerless syringes 10 and lOA of the present 4 invention being filled as described above and oriented vertically with the tab extending upwardly, the head space will reside in the 6 over-fill chamber 30 of the tab 18 and air in the contained fluid 7 will migrate into the over-fill chamber 30. Accordingly, upon the 8 tab being removed with the syringe being oriented in the vertical 9 position, the bellows chambers 22 and 22A and the passageway 24 of the cannula 14 will be filled with fluid containing substantially 11 no air and the risk of an air embolism will be substantially 12 eliminated. Lastly, it will be understood that by eliminating 13 physically separate or physically distinct parts, such as a 14 separate plunger, the plungerless syringe of the present invention renders it suitable for gamma irradiation sterilization.
16 It will be further understood by those skilled in the art that 17 many modifications and variations may be made in the present 18 invention without departing from the spirit and the scope thereof.
i
8 Description of the Prior Art --9 Syringes are well known to the art which include a substantially transparent plastic cylindrical tube providing a ll fluid receiving chamber, a plastic plunger mounted slidably in one 12 end of the tube and a metal needle mounted to the other end of the 13 tube. The plunger is withdrawn to create a vacuum and draw fluid 14 into the chamber after which the plunger is forced into the chamber to expel or eject the fluid through the needle. Typically, the 16 plunger and cylindrical member are disposable, but the metal needle 17 typically is reusable and must be removed from the tube for 18 resterilization prior to reuse. Removal of the needle is well l9 known for the possibility of the user being pricked or stuck by the needle with the highly undesirable attendant possibility of 21 infectious disease transmission.
22 Plungerless syringes are known to the art, such as for example 23 the plungerless syringe disclosed in U.S. Patent No. 5,102,398, 24 entitled PLUNGERLESS SYRINGE, and patented April 7, 1992, Barry L.
Farris inventor. This plungerless syringe is disclosed as 26 providing substantially bubbleless fluid ejection or expulsion by 27 the employment of an air chamber attached to the bellows portion of 2 1 S 6 8 1 ~
:
1 the syringe and which air chamber is taught as being for entrapping 2 air contained in the fluid.
3 As further known to those in the art, the plunger of the prior 4 art plunger syringe, noted above, is initially partially depressed to expel some fluid from the syringe so as to purge air from the 6 adapter or fluid delivery device, such as a needle or catheter, to 7 which the syringe is connected thereby reducing, or substantially 8 eliminating, the possibility of the injection of air into a 9 person's blood stream with the attendant possible air embolism.
The construction of the typical prior art plungerless syringe is 11 such that it does not lend itself to two distinct stages of fluid 12 expulsion including a first stage for expelling a portion of the 13 fluid in the syringe to purge air from the delivery system and a 14 second stage for expelling the remaining fluid contained in the syringe.
16 Accordingly, there exists a need for a plungerless syringe 17 providing for two stages of collapse, an initial or purge stage 18 where air contained in the fluid delivery device to which the 19 syringe is attached is purged, and a second flush stage where the remaining fluid in the syringe is expelled.
21 The prior art plunger syringe, noted above, is also used to 22 determine whether the needle has been properly inserted into a 23 blood vessel of a patient. This is accomplished by partially 24 depressing the plunger to expel a portion of the fluid contained in the syringe after which the plunger is withdrawn to reflux the 26 previously expelled fluid and to withdraw a blood sample into the , . ' 2ls68ll 1 transparent syringe which provides a visible determination that the 2 tip of the needle is in fact in a blood vessel. The plungerless 3 syringes known to the prior art do not include any structure 4 permitting such fluid reflux and blood sample withdrawal and hence cannot be used to determine if the needle tip is properly inserted 6 into a blood vessel.
7 Accordingly, there exists a need for a plungerless syringe 8 provided with structure permitting the reflux of previously 9 expelled fluid and a blood sample to determine whether the tip of the needle attached to the plungerless syringe is properly inserted 11 into a blood vessel.
12 Still further, the typical prior art plunger syringe is 13 relatively expensive to manufacture because it must be manufactured 14 in several steps and assembled and frequently lubrication is required.
16 Accordingly, there exists a need in the art for a plungerless 17 syringe which is relatively inexpensive to manufacture, contains no 18 moving parts making the plungerless syringe suitable for radiation 19 and sterilization.
Summary of the Invention 21 It is the object of the present invention to satisfy the 22 foregoing needs in the art.
23 A plungerless syringe satisfying the foregoing needs and 24 embodying the present invention may include cannula and bellows portions, the bellows portion providing a bellows chamber for 26 receiving fluid which is expelled through a passageway formed in 2l~c8l ~
1 the cannula upon the bellows portion being collapsed. The bellows 2 portion may be provided with a configuration causing the bellows 3 portion to collapse by inversion instead of compression. A tab may 4 be provided at the outer end of the cannula portion which provides a chamber permitting the bellows chamber to be over-filled and 6 which provides a head space for receiving air contained in the 7 fluid which head space is isolated from the bellows chamber. The 8 bellows portion may include a first bellows portion providing a 9 purge stage which upon being collapsed expels a portion of the fluid contained in the bellows chamber to purge air from fluid 11 delivery apparatus, such as a needle, catheter or adapter, 12 connected to the cannula portion; the bellows portion may include 13 a second bellows portion providing a flush stage which upon being 14 collapsed expels the remaining fluid contained in the bellows chamber. The rearward portion of the bellows portion may include 16 a push-button member for being pulled rearwardly to reextend the 17 first bellows portion after its collapse in the purge stage to re-18 draw or reflux into the bellows chamber fluid previously expelled 19 during the purge stage to test whether the tip of a needle attached to the syringe is inserted into a blood vessel. Additionally, the 21 bellows portion may include mechanical snap members which retain 22 the bellows portion fully collapsed stage to prevent unintentional 23 reflux of previously expelled fluid.
24 Description of the Drawings FIG. 1 is a side view of a plungerless syringe embodying the 26 present invention;
21S~g 1-1 `
" -1 FIG. 2 is a side view showing the plungerless syringe of FIG.
2 1 rotated 90;
3 FIG. 3 shows the tab portion removed from the bellows and 4 cannula portions of the plungerless syringe;
S FIG. 4 is a diagrammatical view illustrating the manner in 6 which the plungerless syringe of the present invention is held by 7 a user to collapse of the bellows portion of the syringe to expel 8 or inject fluid into a fluid delivery device such as a needle;
9 FIG. 5 is a vertical cross-sectional view of a mold illustrating the forming of a portion of the plungerless syringe;
11 FIG. 6 is a vertical cross-sectional view illustrating the 12 filling of a portion of the plungerless syringe;
13 FIG. 7 is a vertical cross-sectional view of a mold 14 illustrating the forming of a second portion of the plungerless syringe;
16 FIG. 8 is a vertical cross-sectional view illustrating sealing 17 together of the previously formed two portions of the plungerless 18 syringe;
19 FIG. 9 is a side view of the plungerless syringe of the present invention with the tab portion removed in preparation for 21 fluid expulsion or injection;
22 FIG. 10 illustrates the partial collapse of the bellows in the 23 fluid purge stage;
24 FIG. 11 illustrates the further collapse of the bellows in the fluid flush stage;
~1S681,~
1 FIG. 12 illustrates the mechanical snap-fit for maintaining 2 the bellows fully collapsed to permit unintentional fluid reflux;
3 FIG. 13 is a side view of an alternate embodiment of a 4 plungerless syringe embodying the present invention;
FIG. 14 is a side view of the alternate embodiment of the 6 plungerless syringe of FIG. 13 with the tab portion removed in 7 preparation for fluid expulsion or injection;
8 FIG. 15 illustrates the partial collapse of the bellows in the 9 fluid purge stage;
FIG. 16 illustrates a further collapse of the bellows in the 11 fluid flush stage; and 12 FIG. 17 illustrates the position of the bellows in the final 13 collapse stage.
14 Description of the Preferred Embodiment Referring to the drawings and in particuiar to FIGS. 1-3, a 16 plungerless syringe embodying the present invention is shown and 17 indicated by general numerical designation 10; the plungerless 18 syringe is particularly useful for expelling or injecting fluids 19 such as a saline solution, drugs or other fluids typically injected by a syringe into a needle or catheter. The syringe 10 includes a 21 rearward hollow, collapsible, bellows portion indicated by general 22 numerical designation 12, a forward cannula portion 14, a generally 23 semi-spherical dome portion 16 intermediate the bellows portion 12 24 and the cannula portion 14 for substantially receiving the bellows portion upon being collapsed and decreasing in diameter toward the 26 cannula portion, a removable or break-away tab 18 initially secured '. ` 2ls68lq 1 or sealed to the outer tip 19 of the cannula portion 14 and a 2 rearward disk-like or push-button portion 20. The bellows portion 3 12 provides an internal or bellows chamber 22 for receiving fluid 4 to be expelled or in~ected and the cannula portion 14 includes a passageway 24 in fluid communication with the internal chamber 22 6 and through which passageway fluid contained in the chamber is 7 expelled upon the bellows portion 12 being collapsed. The bellows 8 portion 12 includes a first or rearward bellows portion 26 and a 9 second or forward bellows portion 28 and is made of a suitable substantially transparent flexible plastic material described in 11 detail below. The tab 18 provides an over-fill chamber 30 in fluid 12 communication with the cannula passageway 24 and the internal 13 bellows chamber 22 an d which over-fill chamber 30 permits the over-14 filling of the internal bellows chamber 22 and the cannula lS passageway 24 with fluid in the manufacture of the syringe 10 and 16 isolates the head space inherent in any fluid filling operation to 17 the over-fill chamber 30. As will be described in detail below, 18 this isolation of the head space is particularly beneficial in the 19 substantial elimination of the risk of an air embolism because it eliminates head space in the bellows chamber 22 and the cannula 21 passageway 24 which head space is inherent in any fluid filling 22 operation such as when the plungerless syringe is filled with 23 fluid. Thus, it will be understood, when the tab 18 is removed 24 from the cannula portion 14 by being pulled away as indicated by the arrow 31 and twisted as indicated by the arrow 32 in FIG. 3, 26 the tab portion is removed from the cannula portion and the bellows ~' 21~68~
1 chamber 22 and cannula passageway 24 are fluid-filled and ready for 2 use.
3 The cannula tip 19 is formed in the shape of a male luer 4 connector so as to be compatible with a female luer connector typically provided at the hub of a needle or catheter.
6 Referring to FIG. 4, upon the tab 18 being removed as shown in 7 FIG. 3 and described above, the user grasps or holds the bellows 8 portion 12 by placing the index and middle finger around the dome 9 portion 16 and by placing the thumb on the push-button 20. The cannula tip 19 may be previously inserted into the hub portion 33 11 of the needle 34 and the user's thumb is pressed inwardly to apply 12 inwardly acting force indicated by the arrow 35 in FIG. 4 to 13 compress the bellows portion 12 and expel fluid from the syringe 14 into and through the needle 34.
Referring now to FIGS. 5-8 and first to FIG. 5, the 16 plungerless syringe 10 of the present invention may be manufactured 17 in three stages from substantially transparent polyethylene, 18 polypropylene, or blends thereof, or other flexible resin, to make 19 the syringe 10 substantially transparent permitting the user to observe fluid within the bellows chamber 22, the cannula passageway 21 24 and the over-fill chamber 30; such transparency also permits the 22 user to observe the intentional reflux of fluid into the syringe 23 and the withdrawing of blood from a blood vessel determining that 24 the tip of the needle connected to the syringe is properly inserted into a blood vessel. A first stage of manufacture is illustrated 26 in FIG. 5 wherein the bellows portions 12, cannula portion 14, , ' 21~81~
1 push-button portion 20 and a portion 18' of the removable tab 18 2 are formed from the noted plastic materials in a suitable mold 40 3 such as, for example, by a suitable blow molding operation. It 4 will be particularly noted that the tab portion 18' includes an inner portion 42 which is formed integrally with the cannula tip 19 6 thereby initially attaching or mounting the tab portion 18 to the 7 cannula tip 19. It will be understood that the tab portion 42 and 8 the cannula tip 19 are formed integrally in a relatively thin 9 circular ring-like portion, or frangible edge, which may be readily broken to remove the tab 18 from the cannula tip 19 as shown in 11 FIG. 3 and described above.
12 After the first manufacturing stage illustrated in FIG. 5, 13 suitable filling apparatus, not shown except for a filling tube 44, 14 is placed over the mold 40 and the internal bellows chamber 22, the cannula passageway 24, and a portion 30' of the over-fill chamber 16 30 (FIGS. 1-3) are filled with a suitable injectable fluid 46 of 17 the type noted above. It will be noted particularly that the top 18 or fill line of the fluid 46 resides above the cannula tip 19 and 19 resides in the portion 30' of the over-fill chamber 30. Thereafter the fluid filling apparatus is removed.
21 The upper portion 18" of the tab 18 (FIGS. 1-3) may be 22 suitably formed from the noted plastic materials such as by blow 23 molding in a suitable mold 48. The tab portion 18" is formed to 24 include a portion 30" of the over-fill chamber 30 (FIGS. 1-3).
Thereafter, the molds 48 and 40 are brought into engagement as 26 shown in FIG. 8 and the portions 18' and 18" of the tab 18 are ' ' 21~6814 -1 integrated or sealed together with suitable heat and pressure, or 2 by sonic welding, as known to the art for joining separate plastic 3 parts.
4 Referring now to FIGS. 9-12 and in detail to the operation of the plungerless syringe 10 of the present invention, it will be 6 assumed that the tab 18 has been broken away or removed from the 7 cannula tip 19 as shown in FIG. 3 and described above and that the 8 cannula tip 19 has been inserted, for example, into the hub portion 9 33 of the needle 34 shown in FIG. 4; the needle 34 is not shown in FIGS. 5-12 for convenience of illustration. The syringe 10 will be 11 grasped or held by the user as shown in FIG. 4 and inwardly acting 12 force 35 will be applied to the push-button portion 20 as shown in 13 FIG. 10 to collapse the rearward or first bellows portion 26 and 14 expel a portion of the fluid contained in the internal chamber 22 through the cannula passageway 24 and the needle 34 (FIG. 4).
16 Collapse of the rearward bellows portion 28 provides the purge 17 stage noted above and expels air present in the needle 34 or other 18 fluid delivery device which may be attached to the cannula tip 19.
19 After the purge stage, the tab portion 20 may be grasped by the fingers of the other hand of the user (not shown) to pull the tab 21 portion 20 outwardly or rearwardly as indicated by the arrow 50 in 22 FIG. 10, to re-expand or uncollapse the first bellows portion 26 23 into the uncollapsed position shown in FIG. 9 to reflux or aspirate 24 the fluid expelled in the purge stage and to draw into at least the cannula passageway 24 a sample of blood to determine if the tip of 26 the needle is properly inserted into a blood vessel. Accordingly, _ 10--21~G81 i -1 it will be understood that the tab 20 is also an aspiration tab and 2 that the re-expansion of the first bellows portion 26 is an 3 aspiration stage.
4 Thereafter, the inwardly directed force 35 is applied again to the tab 20 as illustrated in FIG. 11 to re-collapse the first 6 bellows portion 26 and to collapse the second bellows portion 28 in 7 the flush stage to expel the fluid contained in the chamber 22 8 through the cannula passageway 24 and through the needle 34 (FIG.
9 4).
Referring again to FIG. 9, it will be noted that the tab 11 portion 20 is provided with a diameter D1 and that the rearward 12 portion of the dome portion 16 provided with a diameter D2. The 13 diameter D1 is larger than the diameter D2 and in an embodiment of 14 the plungerless syringe of the present invention the diameter D1 is 0.458 inch and the diameter D2 is 0.418 inch. Accordingly, upon 16 continued application of the force 35 after collapse of the bellows 17 portion 12, FIG. 12, the disk-like or push-button portion 20 is 18 forced and wedged into the dome portion 16 to maintain the bellows 19 portion 12 collapsed, and thereby prevent unintentional reflux of previously expelled fluid into the syringe 10; it will be noted 21 from FIG. 12 that upon collapse the bellows portion 12 is 22 substantially contained in the dome portion 16.
23 - Referring again to FIG. 2, it will be noted that the forward 24 bellows portion 28 is defined by a wall having a thickness Tl and that the rearward bellows portion 26 is defined by a wall having a 26 thickness T2 and it will be understood that the thickness T2 is ,~ . 21S6~14 1 less than the thickness T1. This difference in wall thickness 2 facilitates collapse of the bellows portion 12 by inversion, 3 instead of compression, as shown particularly in FIG. 12. It has 4 been discovered that collapse of the bellows portion 12 by inversion, instead of compression, is highly desirable because it 6 reduces the possibility of unintentional fluid reflux subsequent to 7 complete collapse of the bellows portion 12. Such inadvertent 8 reflux is undesirable, since it may result in reduced fluid 9 delivery efficiency and can undesirably draw blood into the needle and syringe after total bellows collapse or undesirably draw 11 previously expelled fluid and blood into the fluid delivery device, 12 such as a needle or catheter, connected to the syringe, and such 13 inadvertent reflux can create a vacuum in the needle or other fluid 14 delivery intravenous access device, such as a catheter, which may result in blood reflux into the catheter. Reflux is undesirable 16 because it may result in clot formation within the catheter line.
17 It will be still further understood that the bellows portion 18 12 of the plungerless syringe 10 of the present invention may be 19 fully collapsed in a single step into the position shown in FIG. 12 without the sequential performance of the purge stage and then the 21 flush stage and without the performance of the aspiration step 22 noted above.
23 Referring now to FIGS. 13-17, an alternate embodiment plunger 24 syringe embodying the present invention is shown and indicated by general numerical designation lOA. It will be generally understood 26 that the plungerless syringe lOA is substantially similar to the 21~8~
1 earlier embodiment plungerless syringe 10 and performs 2 substantially the same function in substantially the same way 3 except that plungerless syringe lOA collapses, not by inversion, 4 but instead by compression, does not include the dome portion 16 and the wall thickness of the bellows portion 28A is substantially 6 uniform and does not vary in thickness as does the wall thickness 7 of the bellows portion 28 of embodiment 10. Accordingly, for 8 convenience of presentation and understanding, structural elements 9 comprising plungerless syringe lOA which are the same as the structural elements in plungerless syringe 10 are given the same 11 numerical designations and have the same function.
12 The bellows portion 12A includes a first or rearward portion 13 26A and a second or forward bellows portion 28A and is made of a 14 suitable substantially transparent flexible plastic material as described above for the construction of the bellows 12.
16 Referring to FIGS. 14-17, the rearward or first bellows 17 portion 26A collapses by compression upon the application of the 18 force 35 to the push-button 20 and, as with the first bellows 19 portion 26 of embodiment 10, such collapse expels a portion of the fluid contained in the internal chamber 22A provided by the first 21 and second bellows portions for the same purpose as described 22 above. Afterwards, as explained above, the push-button 20 may be 23 pulled rearwardly by the force 50 shown in FIG. 15 to reflux a 24 portion of the previously expelled fluid as described above and for the same reason. A further application of the force 35, FIGS. 16 26 and 17, expels the balance of the fluid contained in the chamber . ' 21~81~
1 22A and the bellows portion 28A, including first and second bellows 2 portions, collapses by compression into the final expulsion 3 position shown in FIG. 17.
4 It will be further understood that the plungerless syringe embodiment lOA may be made in the same manner as illustrated above 6 for embodiment 10 and as described above and illustrated in FIGS.
7 5-8.
8 Significantly, it will be understood that the removable or 9 break-away tab 18 of embodiment lOA performs the same over-fill and head space isolation function as the correspondingly numbered tab-11 portion 18 of FIGS. 1-3.
12 Referring again to FIGS. 1-3 and 13, it will be noted that the13 tab 18 is relatively large in size and flange-like in shape and the14 size of the tab 18 discourages touch contamination of the tip 19 ofthe cannula 14 upon the tab 18 being removed as shown in FIGS. 3 16 and 14. The bulb shape of the over-fill tab chamber 30 also 17 discourages touch contamination by distancing the fingers from the 18 luer tip.
19 It will be still further understood that while it is possible for the tab 18 to be removed from the tip of the cannula 14 with 21 the plungerless syringe oriented in a horizontal position wherein, 22 of course, the head space could migrate to the bellows portion 22, 23 this is highly unlikely since the loss of fluid from the syringe 24 would be obvious to a user and a user will naturally or normally orient the plungerless syringes 10 and lOA in the vertical position 26 with tab 18 extending upwardly and will do so through the natural t $~81 1 1 inclination of a person opening a fluid filled container to open 2 the container in the vertical position to prevent fluid spillage.
3 Thus, upon the plungerless syringes 10 and lOA of the present 4 invention being filled as described above and oriented vertically with the tab extending upwardly, the head space will reside in the 6 over-fill chamber 30 of the tab 18 and air in the contained fluid 7 will migrate into the over-fill chamber 30. Accordingly, upon the 8 tab being removed with the syringe being oriented in the vertical 9 position, the bellows chambers 22 and 22A and the passageway 24 of the cannula 14 will be filled with fluid containing substantially 11 no air and the risk of an air embolism will be substantially 12 eliminated. Lastly, it will be understood that by eliminating 13 physically separate or physically distinct parts, such as a 14 separate plunger, the plungerless syringe of the present invention renders it suitable for gamma irradiation sterilization.
16 It will be further understood by those skilled in the art that 17 many modifications and variations may be made in the present 18 invention without departing from the spirit and the scope thereof.
i
Claims (13)
1 Syringe apparatus, comprising:
a cannula portion and a collapsible bellows portion, the cannula portion including a passageway extending therethrough and the bellows portion providing an internal chamber in fluid communication with the passageway, the internal chamber for receiving fluid which is expelled through the passageway upon collapse of the bellows portion, the cannula portion including an outer end; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
a cannula portion and a collapsible bellows portion, the cannula portion including a passageway extending therethrough and the bellows portion providing an internal chamber in fluid communication with the passageway, the internal chamber for receiving fluid which is expelled through the passageway upon collapse of the bellows portion, the cannula portion including an outer end; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
2. Plungerless syringe, comprising:
a collapsible bellows portion and a cannula portion, the collapsible bellows portion providing an internal chamber for receiving fluid and the cannula portion provided with an internal passageway in fluid communication with the internal chamber and through which passageway the fluid is expelled;
the cannula portion including an outer end for being connected to apparatus for receiving the fluid;
the bellows portion including a first bellows portion providing a purge stage and which upon being collapsed expels a portion of fluid contained in the internal chamber through the passageway to purge air from apparatus attached to the outer end of the cannula portion; and the bellows portion including a second bellows portion providing a flush stage and which upon being collapsed expels the remaining fluid in the internal chamber through the passageway.
a collapsible bellows portion and a cannula portion, the collapsible bellows portion providing an internal chamber for receiving fluid and the cannula portion provided with an internal passageway in fluid communication with the internal chamber and through which passageway the fluid is expelled;
the cannula portion including an outer end for being connected to apparatus for receiving the fluid;
the bellows portion including a first bellows portion providing a purge stage and which upon being collapsed expels a portion of fluid contained in the internal chamber through the passageway to purge air from apparatus attached to the outer end of the cannula portion; and the bellows portion including a second bellows portion providing a flush stage and which upon being collapsed expels the remaining fluid in the internal chamber through the passageway.
3 Plungerless syringe, comprising:
a collapsible bellows including forward and rearward portions and providing an internal chamber for receiving fluid and a cannula provided with a passageway in fluid communication with the internal chamber and through which passageway fluid is expelled upon collapse of the bellows;
the bellows provided with a configuration causing said bellows portion to collapse by inversion upon being compressed;
the cannula including an outer end for being connected to apparatus for receiving expelled fluid;
the bellows including a first bellows portion providing a purge stage and upon the first bellows portion being collapsed a portion of the fluid contained in the chamber is expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
the bellows portion including a second bellows portion providing a flush stage and upon the second bellows portion being collapsed the fluid remaining in the chamber after collapse of the first bellows portion is expelled through the cannula portion passageway; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
a collapsible bellows including forward and rearward portions and providing an internal chamber for receiving fluid and a cannula provided with a passageway in fluid communication with the internal chamber and through which passageway fluid is expelled upon collapse of the bellows;
the bellows provided with a configuration causing said bellows portion to collapse by inversion upon being compressed;
the cannula including an outer end for being connected to apparatus for receiving expelled fluid;
the bellows including a first bellows portion providing a purge stage and upon the first bellows portion being collapsed a portion of the fluid contained in the chamber is expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
the bellows portion including a second bellows portion providing a flush stage and upon the second bellows portion being collapsed the fluid remaining in the chamber after collapse of the first bellows portion is expelled through the cannula portion passageway; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
4. Plungerless syringe, comprising:
a rearward generally cylindrical push-button portion, a forward generally cylindrical and longitudinally extending cannula portion, and a bellows portion intermediate said rearward push-button portion and said cannula portion;
said bellows portion providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
upon said bellows portion being at least partially collapsed by force acting inwardly against said rearward push-button portion at least a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway; and said rearward push-button portion for being pulled rearwardly to cause intentional reflux of previously expelled fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion.
a rearward generally cylindrical push-button portion, a forward generally cylindrical and longitudinally extending cannula portion, and a bellows portion intermediate said rearward push-button portion and said cannula portion;
said bellows portion providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
upon said bellows portion being at least partially collapsed by force acting inwardly against said rearward push-button portion at least a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway; and said rearward push-button portion for being pulled rearwardly to cause intentional reflux of previously expelled fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion.
5. Plungerless syringe, comprising:
a rearward generally cylindrical push-button portion, a forward generally cylindrical and longitudinally extending cannula portion, and a bellows portion intermediate said rearward push-button portion and said cannula portion;
said bellows portion being hollow and providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
said bellows portion including a first bellows portion adjacent said rearward push-button portion and providing a purge stage and upon said first bellows portion being collapsed by force acting inwardly against said rearward push-button portion a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
said rearward push-button portion for being pulled rearwardly to cause intentional reflux of fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion;
said bellows portion including a second bellows portion intermediate said first bellows portion and said dome portion and providing a flush stage and upon the second bellows portion being collapsed by force acting inwardly against said rearward push-button portion fluid remaining in the internal chamber after collapse of said first bellows portion being expelled through the cannula portion passageway; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
a rearward generally cylindrical push-button portion, a forward generally cylindrical and longitudinally extending cannula portion, and a bellows portion intermediate said rearward push-button portion and said cannula portion;
said bellows portion being hollow and providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
said bellows portion including a first bellows portion adjacent said rearward push-button portion and providing a purge stage and upon said first bellows portion being collapsed by force acting inwardly against said rearward push-button portion a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
said rearward push-button portion for being pulled rearwardly to cause intentional reflux of fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion;
said bellows portion including a second bellows portion intermediate said first bellows portion and said dome portion and providing a flush stage and upon the second bellows portion being collapsed by force acting inwardly against said rearward push-button portion fluid remaining in the internal chamber after collapse of said first bellows portion being expelled through the cannula portion passageway; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
6. Plungerless syringe, comprising:
bellows portion providing an internal chamber for receiving fluid and cannula portion provided with a passageway in fluid communication with the chamber and through which fluid is expelled upon collapse of the bellows portion; and mechanical snap fastening means for maintaining the bellows portion collapsed to prevent reflux of previously expelled fluid into the cannula portion passageway.
bellows portion providing an internal chamber for receiving fluid and cannula portion provided with a passageway in fluid communication with the chamber and through which fluid is expelled upon collapse of the bellows portion; and mechanical snap fastening means for maintaining the bellows portion collapsed to prevent reflux of previously expelled fluid into the cannula portion passageway.
7. Plungerless syringe, comprising:
a collapsible bellows including forward and rearward portions and providing an internal chamber for receiving fluid and a cannula provided with a passageway in fluid communication with the internal chamber and through which passageway fluid is expelled upon collapse of the bellows;
the bellows provided with a configuration causing said bellows portion to collapse by inversion upon being compressed;
the cannula including an outer end for being connected to apparatus for receiving expelled fluid;
upon said rearward bellows portion being collapsed a portion of the fluid contained in the chamber is expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
upon said forward bellows portion being collapsed the fluid remaining in the chamber after collapse of the first bellows portion is expelled through the cannula portion passageway;
engageable members for being wedged together in a snap fit to maintain the bellows collapsed after collapse of both the first and second bellows portions; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
a collapsible bellows including forward and rearward portions and providing an internal chamber for receiving fluid and a cannula provided with a passageway in fluid communication with the internal chamber and through which passageway fluid is expelled upon collapse of the bellows;
the bellows provided with a configuration causing said bellows portion to collapse by inversion upon being compressed;
the cannula including an outer end for being connected to apparatus for receiving expelled fluid;
upon said rearward bellows portion being collapsed a portion of the fluid contained in the chamber is expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
upon said forward bellows portion being collapsed the fluid remaining in the chamber after collapse of the first bellows portion is expelled through the cannula portion passageway;
engageable members for being wedged together in a snap fit to maintain the bellows collapsed after collapse of both the first and second bellows portions; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
8. Plungerless syringe, comprising:
a rearward generally cylindrical push-button portion, a forward generally cylindrical and longitudinally extending cannula portion, a generally semi-spherical dome portion attached to and decreasing in diameter toward said cannula portion, and a bellows portion attached to and intermediate said rearward push-button portion and said dome portion;
said bellows portion providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
upon said bellows portion being at least partially collapsed by force acting inwardly against said rearward push-button portion at least a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway; and said rearward push-button portion for being pulled rearwardly to cause intentional reflux of previously expelled fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion.
a rearward generally cylindrical push-button portion, a forward generally cylindrical and longitudinally extending cannula portion, a generally semi-spherical dome portion attached to and decreasing in diameter toward said cannula portion, and a bellows portion attached to and intermediate said rearward push-button portion and said dome portion;
said bellows portion providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
upon said bellows portion being at least partially collapsed by force acting inwardly against said rearward push-button portion at least a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway; and said rearward push-button portion for being pulled rearwardly to cause intentional reflux of previously expelled fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion.
9. Plungerless syringe, comprising:
a rearward generally cylindrical push-button portion, a forward generally cylindrical and longitudinally extending cannula portion, a generally semi-spherical dome portion attached to and decreasing in diameter toward said cannula portion, and a bellows portion intermediate said rearward push-button portion and said dome portion;
said bellows portion and said dome portion being hollow and providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
said bellows portion including a first bellows portion adjacent said rearward push-button portion and providing a purge stage and upon said first bellows portion being collapsed by force acting inwardly against said rearward push-button portion a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
said rearward push-button portion for being pulled rearwardly to cause intentional reflux of fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion;
said bellows portion including a second bellows portion intermediate said first bellows portion and said dome portion and providing a flush stage and upon the second bellows portion being collapsed by force acting inwardly against said rearward push-button portion fluid remaining in the internal chamber after collapse of said first bellows portion being expelled through the cannula portion passageway;
said rearward push-button portion having a first diameter and said dome portion including a rearward portion having a second diameter smaller than said first diameter and upon said first and second bellows portions being collapsed said rearward push-button portion being wedged into said dome rearward portion to maintain said bellows portion collapsed to prevent unintentional reflux of expelled fluid into said cannula portion passageway; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
a rearward generally cylindrical push-button portion, a forward generally cylindrical and longitudinally extending cannula portion, a generally semi-spherical dome portion attached to and decreasing in diameter toward said cannula portion, and a bellows portion intermediate said rearward push-button portion and said dome portion;
said bellows portion and said dome portion being hollow and providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
said bellows portion including a first bellows portion adjacent said rearward push-button portion and providing a purge stage and upon said first bellows portion being collapsed by force acting inwardly against said rearward push-button portion a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
said rearward push-button portion for being pulled rearwardly to cause intentional reflux of fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion;
said bellows portion including a second bellows portion intermediate said first bellows portion and said dome portion and providing a flush stage and upon the second bellows portion being collapsed by force acting inwardly against said rearward push-button portion fluid remaining in the internal chamber after collapse of said first bellows portion being expelled through the cannula portion passageway;
said rearward push-button portion having a first diameter and said dome portion including a rearward portion having a second diameter smaller than said first diameter and upon said first and second bellows portions being collapsed said rearward push-button portion being wedged into said dome rearward portion to maintain said bellows portion collapsed to prevent unintentional reflux of expelled fluid into said cannula portion passageway; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
10. Syringe apparatus, comprising:
a cannula portion and a collapsible bellows portion, the cannula portion including a passageway extending therethrough and the bellows portion providing an internal chamber in fluid communication with the passageway, the internal chamber for receiving fluid which is expelled through the passageway upon collapse of the bellows portion; and the bellows portion provided with a predetermined structure causing the bellows portion to collapse by inversion.
a cannula portion and a collapsible bellows portion, the cannula portion including a passageway extending therethrough and the bellows portion providing an internal chamber in fluid communication with the passageway, the internal chamber for receiving fluid which is expelled through the passageway upon collapse of the bellows portion; and the bellows portion provided with a predetermined structure causing the bellows portion to collapse by inversion.
11. Syringe apparatus, comprising:
a cannula portion and a collapsible bellows portion, the cannula portion including a passageway extending therethrough and the bellows portion providing an internal chamber in fluid communication with the passageway, the internal chamber for receiving fluid which is expelled through the passageway upon collapse of the bellows;
the bellows portion including forward and rearward portions, the forward portion disposed toward the cannula portion; and the forward bellows portion defined by a wall having a first thickness and the rearward bellows portion defined by a wall having a second thickness thinner than said first thickness, upon the bellows portion being collapsed the rearward portion collapsing before the forward portion and the difference in wall thickness facilitating collapse of the bellows portion by inversion.
a cannula portion and a collapsible bellows portion, the cannula portion including a passageway extending therethrough and the bellows portion providing an internal chamber in fluid communication with the passageway, the internal chamber for receiving fluid which is expelled through the passageway upon collapse of the bellows;
the bellows portion including forward and rearward portions, the forward portion disposed toward the cannula portion; and the forward bellows portion defined by a wall having a first thickness and the rearward bellows portion defined by a wall having a second thickness thinner than said first thickness, upon the bellows portion being collapsed the rearward portion collapsing before the forward portion and the difference in wall thickness facilitating collapse of the bellows portion by inversion.
12. Plungerless syringe, comprising:
a rearward portion, a forward generally cylindrical and longitudinally extending cannula portion, and a bellows portion intermediate said rearward portion and said cannula portion;
said bellows portion providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
upon said bellows portion being at least partially collapsed by force acting inwardly against said rearward portion at least a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway; and said rearward portion for being pulled rearwardly to aspirate said previously expelled fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion.
a rearward portion, a forward generally cylindrical and longitudinally extending cannula portion, and a bellows portion intermediate said rearward portion and said cannula portion;
said bellows portion providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
upon said bellows portion being at least partially collapsed by force acting inwardly against said rearward portion at least a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway; and said rearward portion for being pulled rearwardly to aspirate said previously expelled fluid into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion.
13. Plungerless syringe, comprising:
a rearward portion, a forward generally cylindrical and longitudinally extending cannula portion, and a bellows portion intermediate said rearward portion and said cannula portion;
said bellows portion being hollow and providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
said bellows portion including a first bellows portion adjacent said rearward portion and providing a purge stage and upon said first bellows portion being collapsed by force acting inwardly against said rearward portion a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
said rearward portion for being pulled rearwardly to aspirate said fluid previously expelled in said purge stage into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion;
said bellows portion including a second bellows portion intermediate said first bellows portion and said cannula portion and providing a flush stage and upon the second bellows portion being collapsed by force acting inwardly against said rearward portion fluid remaining in the internal chamber after collapse of said first bellows portion being expelled through the cannula portion passageway; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
a rearward portion, a forward generally cylindrical and longitudinally extending cannula portion, and a bellows portion intermediate said rearward portion and said cannula portion;
said bellows portion being hollow and providing an internal chamber for receiving fluid and said cannula portion provided with a passageway extending longitudinally therethrough and in fluid communication with said internal chamber;
said cannula portion including an outer end for being connected to apparatus for receiving fluid expelled from the internal chamber;
said bellows portion including a first bellows portion adjacent said rearward portion and providing a purge stage and upon said first bellows portion being collapsed by force acting inwardly against said rearward portion a portion of the fluid contained in the internal chamber being expelled through the cannula portion passageway to purge air contained in apparatus connected to the outer end of the cannula portion;
said rearward portion for being pulled rearwardly to aspirate said fluid previously expelled in said purge stage into the cannula portion passageway to facilitate determination of the continuity of a fluid path including the internal chamber, the cannula portion passageway and apparatus connected to the outer end of the cannula portion;
said bellows portion including a second bellows portion intermediate said first bellows portion and said cannula portion and providing a flush stage and upon the second bellows portion being collapsed by force acting inwardly against said rearward portion fluid remaining in the internal chamber after collapse of said first bellows portion being expelled through the cannula portion passageway; and a removable tab member mounted to the outer end of the cannula portion for initially sealing the passageway to maintain the fluid in the internal chamber and providing an over-fill chamber permitting the internal chamber to be over-filled with fluid and providing head space isolated from the internal chamber for receiving air contained in the fluid.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30707794A | 1994-09-16 | 1994-09-16 | |
US08/307,077 | 1994-09-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2156814A1 true CA2156814A1 (en) | 1996-03-17 |
Family
ID=23188147
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002156814A Abandoned CA2156814A1 (en) | 1994-09-16 | 1995-08-23 | Plungerless syringe |
Country Status (4)
Country | Link |
---|---|
US (1) | US5609580A (en) |
EP (1) | EP0701833A1 (en) |
JP (1) | JPH08299437A (en) |
CA (1) | CA2156814A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113588345A (en) * | 2021-03-25 | 2021-11-02 | 武汉佰美斯医疗科技有限公司 | Liquid taking-out device |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19522451C2 (en) * | 1995-06-21 | 1997-11-06 | Bernd Hansen | Device for dispensing a flowable substance from a container |
US6077252A (en) * | 1997-09-17 | 2000-06-20 | Siegel; Robert | Single or multiple dose syringe |
SK285419B6 (en) * | 1998-09-22 | 2007-01-04 | Fresenius Kabi Ab | Arrangement for storing and administering a medical fluid |
USD432647S (en) * | 1999-02-25 | 2000-10-24 | Barry Farris | No reflux syringe |
USD432646S (en) * | 1999-02-26 | 2000-10-24 | Barry Farris | Syringe with air trap |
US6328715B1 (en) * | 1999-09-21 | 2001-12-11 | William B. Dragan | Unit dose low viscosity material dispensing system |
DE102006009611A1 (en) * | 2006-03-02 | 2007-09-06 | Bernd Hansen | A system for preparing and providing a flowable medium formed by mixing a dry substance with a fluid |
CN101437559B (en) * | 2006-05-04 | 2011-12-14 | 皇家飞利浦电子股份有限公司 | Medical injector |
WO2009044401A2 (en) | 2007-10-02 | 2009-04-09 | Yossi Gross | External drug pump |
US10420880B2 (en) * | 2007-10-02 | 2019-09-24 | West Pharma. Services IL, Ltd. | Key for securing components of a drug delivery system during assembly and/or transport and methods of using same |
US9656019B2 (en) | 2007-10-02 | 2017-05-23 | Medimop Medical Projects Ltd. | Apparatuses for securing components of a drug delivery system during transport and methods of using same |
WO2012061140A1 (en) | 2010-10-25 | 2012-05-10 | Medrad, Inc. | Bladder syringe fluid delivery system |
US9498570B2 (en) | 2010-10-25 | 2016-11-22 | Bayer Healthcare Llc | Bladder syringe fluid delivery system |
US9180252B2 (en) | 2012-04-20 | 2015-11-10 | Bayer Medical Care Inc. | Bellows syringe fluid delivery system |
US10010685B2 (en) * | 2012-06-26 | 2018-07-03 | Becton, Dickinson And Company | Single use delivery device having a primer element |
WO2014090796A1 (en) * | 2012-12-10 | 2014-06-19 | Fresenius Kabi Deutschland Gmbh | Process for producing and assembling a medical operations syringe |
ES2873963T3 (en) | 2014-04-25 | 2021-11-04 | Bayer Healthcare Llc | Rolling Diaphragm Syringe |
CN107847192A (en) | 2015-04-24 | 2018-03-27 | 拜耳医药保健有限公司 | Syringe with rolling diaphragm |
US10149943B2 (en) | 2015-05-29 | 2018-12-11 | West Pharma. Services IL, Ltd. | Linear rotation stabilizer for a telescoping syringe stopper driverdriving assembly |
US10576207B2 (en) | 2015-10-09 | 2020-03-03 | West Pharma. Services IL, Ltd. | Angled syringe patch injector |
US9987432B2 (en) | 2015-09-22 | 2018-06-05 | West Pharma. Services IL, Ltd. | Rotation resistant friction adapter for plunger driver of drug delivery device |
JP7017512B2 (en) | 2015-10-09 | 2022-02-08 | ウェスト ファーマ サービシーズ イスラエル リミテッド | Bending fluid path type accessories for filled fluid containers |
CN113041432B (en) | 2016-01-21 | 2023-04-07 | 西医药服务以色列有限公司 | Medicament delivery device comprising a visual indicator |
EP3711793B1 (en) | 2016-01-21 | 2021-12-01 | West Pharma Services IL, Ltd. | A method of connecting a cartridge to an automatic injector |
JP6542481B2 (en) | 2016-01-21 | 2019-07-10 | ウェスト ファーマ サービシーズ イスラエル リミテッド | system |
US11389597B2 (en) | 2016-03-16 | 2022-07-19 | West Pharma. Services IL, Ltd. | Staged telescopic screw assembly having different visual indicators |
JP6725343B2 (en) * | 2016-07-06 | 2020-07-15 | テルモ株式会社 | Hemostatic device |
JP6869327B2 (en) | 2016-08-01 | 2021-05-12 | ウェスト ファーマ サービシーズ イスラエル リミテッド | Anti-rotation cartridge |
TWI737812B (en) | 2016-09-16 | 2021-09-01 | 美商拜耳保健公司 | Pressure jacket having syringe retaining element and fluid injector for delivering fluid to a patient |
JP7023947B2 (en) | 2016-10-17 | 2022-02-22 | バイエル・ヘルスケア・エルエルシー | Fluid injector with syringe engagement mechanism |
AU2017345167B2 (en) | 2016-10-17 | 2022-12-15 | Bayer Healthcare Llc | Fluid injector with syringe engagement mechanism |
CN110869072B (en) | 2017-05-30 | 2021-12-10 | 西部制药服务有限公司(以色列) | Modular drive mechanism for a wearable injector |
DK3681561T3 (en) | 2017-09-13 | 2022-01-24 | Bayer Healthcare Llc | MOVABLE SPRAYER CAP FOR SEPARATE FILLING AND FEEDING |
RU185468U1 (en) * | 2018-06-29 | 2018-12-05 | Юлай Масабихович Насибуллин | SPRING SYRINGE FOR DISPOSABLE USE |
CN114502214A (en) | 2019-09-10 | 2022-05-13 | 拜耳医药保健有限公司 | Pressure jacket and syringe retention features for angiographic fluid injectors |
EP4106857A1 (en) | 2020-02-21 | 2022-12-28 | Bayer HealthCare, LLC | Fluid path connectors for medical fluid delivery |
AU2021292515A1 (en) | 2020-06-18 | 2022-12-22 | Bayer Healthcare Llc | In-line air bubble suspension apparatus for angiography injector fluid paths |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2667163A (en) * | 1951-10-13 | 1954-01-26 | Arthur E Smith | Unitary syringe |
US2674247A (en) * | 1952-03-06 | 1954-04-06 | Mclellan Charles | Air-pressure teeth cleaner |
US3220412A (en) * | 1958-12-19 | 1965-11-30 | Robert K Mcconnaughey | Holder for hypodermic syringe cartridges |
US3144178A (en) * | 1962-03-12 | 1964-08-11 | Stanley J Sarnoff | Cartridge holder |
GB1095316A (en) * | 1963-08-08 | 1967-12-13 | Arthur Bane | Improvements in ampoules for surgical hypodermic syringes |
GB1175184A (en) * | 1966-02-08 | 1969-12-23 | Arthur Bane | Improvements in Syringe Ampoules. |
US3848593A (en) * | 1970-10-09 | 1974-11-19 | Affiliated Hospital Prod | Side loading disposable carpule syringe |
US3811441A (en) * | 1972-02-10 | 1974-05-21 | Survival Technology | Cartridge syringe |
SE7502318L (en) * | 1975-03-03 | 1976-09-06 | Af Ekenstam Thuresson Bo | PACKAGING FOR LIQUID FOR SEMI-SOLID MATERIAL, SUITABLE FOR SMALLER QUANTITIES |
GB1583157A (en) * | 1976-05-07 | 1981-01-21 | Kenova Ab | Syringes |
US4410323A (en) * | 1980-06-23 | 1983-10-18 | Milton Hodosh | Predosed disposable syringe |
US4411656A (en) * | 1982-01-29 | 1983-10-25 | Urologic & Enteric Research Associates | Compressible syringe |
GB8509301D0 (en) * | 1985-04-11 | 1985-05-15 | Clinical Products Dev Ltd | Device for surgical procedures |
US5102398A (en) | 1990-09-18 | 1992-04-07 | Farris Barry L | Plungerless syringe |
US5242422A (en) * | 1991-11-29 | 1993-09-07 | Professional Medical Products, Inc. | One piece molded syringe with tethered cap |
US5451214A (en) * | 1993-03-22 | 1995-09-19 | Hajishoreh; Kaveh-Karimi | Syringe apparatus |
-
1995
- 1995-07-14 US US08/502,062 patent/US5609580A/en not_active Expired - Lifetime
- 1995-08-23 CA CA002156814A patent/CA2156814A1/en not_active Abandoned
- 1995-09-11 EP EP95114217A patent/EP0701833A1/en not_active Withdrawn
- 1995-09-14 JP JP7262565A patent/JPH08299437A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113588345A (en) * | 2021-03-25 | 2021-11-02 | 武汉佰美斯医疗科技有限公司 | Liquid taking-out device |
Also Published As
Publication number | Publication date |
---|---|
JPH08299437A (en) | 1996-11-19 |
EP0701833A1 (en) | 1996-03-20 |
US5609580A (en) | 1997-03-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0701833A1 (en) | Plungerless Syringe | |
US5538506A (en) | Prefilled fluid syringe | |
JP3665646B2 (en) | Syringe | |
EP1225937B1 (en) | Multiple-dose syringe | |
US6808507B2 (en) | Safety injectors | |
EP1703931B1 (en) | Positive displacement flush syringe | |
US6319235B1 (en) | Syringe serving also as an ampule and associated equipment | |
US4518385A (en) | Disposable syringe for needleless injector | |
US4581023A (en) | Hypodermic syringe assembly | |
US6024727A (en) | Self-retracting medical needle apparatus and methods | |
US5084018A (en) | Safety syringe | |
US5246423A (en) | Remote cannula removal hypodermic syringe | |
US5000735A (en) | Single use syringe | |
IE47621B1 (en) | Syringe | |
MX2007008261A (en) | Positive displacement flush syringe. | |
CN104582767A (en) | Retractable needle safety syringes | |
JPH024374A (en) | Liquid shifting assembly | |
US5833660A (en) | Non-reusable syringe | |
EP0252644A2 (en) | Method and apparatus for catching fluids purged from a syringe | |
US5370626A (en) | Plungerless syringe | |
US5413564A (en) | Predetermined dosage hypodermic syringe system | |
US3380449A (en) | Cartridge with burstable seal | |
US5102398A (en) | Plungerless syringe | |
WO2008097979A2 (en) | Syringe assembly having reuse prevention features |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Discontinued | ||
FZDE | Discontinued |
Effective date: 20000823 |