CA1227392A - Long capillary tube hose assembly for fluid dispensing device - Google Patents

Long capillary tube hose assembly for fluid dispensing device

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Publication number
CA1227392A
CA1227392A CA000471640A CA471640A CA1227392A CA 1227392 A CA1227392 A CA 1227392A CA 000471640 A CA000471640 A CA 000471640A CA 471640 A CA471640 A CA 471640A CA 1227392 A CA1227392 A CA 1227392A
Authority
CA
Canada
Prior art keywords
syringe
hose assembly
cover
block
coupler
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA000471640A
Other languages
French (fr)
Inventor
Jerome E. Strand
Gary A. Thill
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
3M Co
Original Assignee
Minnesota Mining and Manufacturing Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US06/577,757 external-priority patent/US4597754A/en
Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Application granted granted Critical
Publication of CA1227392A publication Critical patent/CA1227392A/en
Expired legal-status Critical Current

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Abstract

Abstract of the Disclosure A hose assembly for use to regulate flow from a dispensing device that provides a generally constant pressure on a liquid to be dispersed. The hose assembly includes a length of capillary tubing through which the liquid must pass as it is dispersed which has a length of at least 45 centimeters and a volume of less than about 0.25 cubic centimeters so that the assembly can provide a slow steady predetermined flow rate while containing a small amount of the liquid being dispensed.

Description

~ 73~ 557-2861 Backqround of the Invention The United States Patents listed above describe a device for dispensing fluid at a slow, uniform rate over a sustained period of time which has a simple, inexpensive structure, is easy -to use, requires no regulation or adjustment by the person using the device, and which is well-safeguarded against tampering or inadvertent improper operation of the device.
The dispensing device described therein comprises a hose assembly adapted to be coupled to a conventional syringe, which hose assembly comprises a length of capillary tubing through which the fluid must pass while being delivered to a patient~ and means for applying a uniform force to the plunger to provide fluid flow through the capillary tube at a slow, steady rate over a long period of time (e.g., less than 60 milliliters per hour).
As stated therein the rate of flow Q in cc/sec through the capillary tuhe can be estimated from Poiseuille's Law expressed in the equation:

Q 81n ,, ~
( ~,, .

` ~ -2 ~ 2 where P is the pressure drop through the tube in dynes/cm2, r is the internal radius of the capillary tube in cm, 1 is the length of the capillary tube in cm, and n is the liquid viscosity in poise. By solving this equation it can be found that capillary tubes of a reasonable length suitable for restricting flow to rates in the range indicated under the influence of pressures of the range of pressures easily developed in a syringe (e.g., about 69,000 to 2,068,400 dynes/cm2) can have bores in the range of about 0.0025 to 0.038 cm. With current technology it is difficult to produce capillary tubing in this size range with bore diameters which deviate less than about 10~ from a nominal diameter, however. Since the rate of flow through a tube is proportional to the fourth power of its diarneter, such a deviation could cause a variation of about -3~% to +~6% in flow rate, which would be unacceptable for most medical uses. By only using long lengths of capillary tubing, however, (i.e., capillary tubes over 2 centimeter in length) much less variation in flow rates is found between different lengths of capillary tubing than is suggested above; perhaps because diameter variations tend to cancel each other along the length of the capillary tubes. With capillary tubing of polytetrafluoroethylene sold under the ~ trade ~ "Teflon" (which is preferred) having a nominal inside diameter in the range of 0.0025 to 0.019 cm, it has been found that lengths of the capillary tubing in excess of 2 cm. normally produce flow rate variations of less than 10%, which is acceptable for medical use of the device described herein.
Hose assem'olies having capillary tubes of different nominal diameters which afford different rates of fluid flow (which rates, for example, may be indicated by color coding of the hose assemblies) can be used interchangeably in the device, and the inexpensive hose assemblies can be clisposed of after use to insure sanitation for medical or other uses.

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One problem presented by the use of such a hose assembly is that in many instances (such as for use in introducing fluids intravenously) prior to activating the device, air must be purged from the hose assembly to preclude air being delivered to the patient. This purging is typically done by attaching the hose asssembly to the syringe outside of the device, and manually activating the syringe until liquid has entirely filled the hose assembly;
after which the syringe is placed in the device and the device is activated to deliver the liquid to the patient at the desired rate.
U.S. Patent No. ~,430,079 teaches that for hose assemblies having small diameter capillary tubing (e.g., 0.0045 to O.Ol cm) adapted to allow only very slow rates of flow (e.g. 0.5 to 15 ml/hr) it is preferred to use a first embodiment of the hose assembly that allows the capillary tubing to be bypassed to afford rapid purging of air from the hose a~sembly with fluid from the syringe. The first hose assembly embodiment includes a metering assembly that provides a coupler between the hose assembly and the syringe. The metering assembly includes the capillary tube and parts moveable between a metering position at which fluid flowing through the metering assembly must pass through the capillary tubing, and a purging position at which fluid propelled by manual operation of the syringe can bypass the capillary tube and flow rapidly through the metering assembly to purge the hose assembly. The device has structure that insures that the metering assembly in this first embodiment of the hose assembly is in its metering position when the dispensing device is activated to preclude operation of the device with the metering assembly in its purge position. Support means included in a frame for the device supports the meterin~ assembly and thereby a syringe couple~ to the metering assembly. The support means is specially adapted so that it will engage and support the metering assembly only when it is in its metering position.
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Also U.S. Patent No. 4,430,079 teaches that for metering devices having larger diameter capillary tubing (e.g. over 0.010 cm) adapted to allow relatively larger rates of flow (e.g. over 15 ml/hr) one oE several other embodiments of the hose asssembly can be used that have no by pass, in which embodiments the capillary tubing may be positioned at the end of the hose assembly opposite the syringe. ~hen the capillary tubing is positioned at the end of the hose assembly opposite the syringe almost all of the air passes through the capillary tube before the liquid reaches it, which, because of the extremely low viscosity of air compared to liquid, allows a fairly rapid purge rate ~e.g. less than about 20 seconds). These other embodiments of the hose assembly include more conventional couplers at their ends adapted to engage the syringe, which couplers are adopted to be received in the support means of the device.
When either of the above described types of hose assemblies is made in a long length (e.~., over 45 centimeters and preferably in the range of 120 to 150 centimeters), however, it has a relatively large internal volume (e.g., 1/2 to 3/4 cubic centimeter) which is quite significant compared to the vol~lme of the syringe from which the liquid is dispersed. Thus persons filling the syringe must add additional liquid to allow for the volume in the hose assembly (which will normally be still filled with the liquid when it i9 disgarded after use) ~hile providing the intended delivered volume of liquid. This is both wasteful of the liquid, and causes an element of uncertainty in forecasting what internal volume the hose assembly wlll have.

Summary of the Invention The invention claimed in this application provides long leng~h ho~e assemblies that can e~fectively meter dispensing liquid flow from the device de~cribed above without containin~ a signiEicant internal volume oE

~2~73~

liquid that must be accounted for in filling of the syringe.
According to the present invention there is provided a hose assembly adapted for use with a fluid dispensing device which applies a generally constant pressure to dispense fluid through the hose assembly, said hose assembly comprising a capillary tube having first and second ends and defining a through passageway between said ends, said capillary tube having a volume of less than about 0.25 cubic centimeter and a length of at least 45 centimeters; and said hose assembly further including a coupler at said first end adapted for releasably attaching caid hose assembly to a said device with an outlet opening of the devlce communicat-ing with said through passageway.
Surprisingly, such capillary tubes can be quite quickly purged of air, and provide quite predictable flow rates, while containing such a small internal volume that no additional liquid need be added to the syringe to compensate for the liquid that is retained in the tube after its use.
The invention also provides a fluid dispensing device adapted Eor engaging a fluid-filled syringe to dispense fluid from the syringe at a slow, steady rate of less than 60 cubic centi-meters per hour, said syringe being cf the type comprising an elongate housing including a tubular wall having an open end and an end wall having an outlet opening at the end of the tubular wall opposi-te its open end, and a plunger having one end portion positioned within and sealing against the inner surface of said tubular wall and an opposite end portion projecting Erom the open : end of said tubular wall, with the fluid being within said tubular ~ wall between said end wall and said plunger, said device compris-~Z~73~2 -6- 5~7-2861 ing: a hose assembly having first and second ends and comprising a capillary tube defining a passageway between said ends, said capillary tube having a volume of less than about 0.25 cubic centimeter and a length of at least about 45 centimeters, and said hose assembly further including a coupler at said first end adapted for releasably attaching said for the capillary tubing to the housi.ng of a said syringe with the outlet opening of the syringe communicating with said passageway; a frame comprising support means adapted for engaging and supporting said coupler;
spring means adapted for applying a uniform force against the plunger of the syringe to cause fluid within said syringe to flow through said hose assembly; and activating means for moving said spring means between a disengaged position spaced from the plunger of a said syringe attached to said coupler to afford insertion or removal of the syringe and said hose assembly, and an engaged position engaged with said plunger to apply said uniform force, said activating means including securing means ~or securing the syringe and the coupler of said hose assembly in said support means when said activating means positions said spring means in said engaged position.
Brief Description of the Drawing The device will ~urther be described with reference to the accompanying drawings wherein like numerals reer to like parts through the several views and wherein:
Figure 1 is a horizontal sectional view of a ~l~id dis-pensing device coupled to a hose assembly according to the present invention, which device has inserted therein a syrin~e frQm wllich fluid is to be dispensed throuyh the hose assembly;

, ~

~L2;~
- -6a- 557-2861 Figure 2 is a sectional view taken approximately along line 2-2 of Figure l;
Figure 3 is an enlarged sectional view taken approxi-mately along line 3-3 of Figure 2;
Figure 4 is an enlarged end view of the fluid dispensing device of Figure l;
Figure 5 is a sectional view taken approximately along line 5-5 of Figure 4 except that a cover for the fluid dispensing device is open, and the hose assembly and ~ .

~2;~3~, the syringe are not inserted in the device;
Figure 6 is a fragmentary sectional view of the hose assembly of Figure 1.

Descri tion of the Preferred Embodiment p Referring now to the drawing, there is illustrated a fluid dispensing device 10 adapted to apply a uniform pressure to a liquid to dispense the liquid through a hose assembly 120 according to the present invention.
The fluid dispensing device 10 is adapted to dispense fluid at a slow, steady rate through the hose assembly 120 over a prolonged period of time from a conventional syringe 12 of the type including an elongate housing 14 with an outlet tube 16 at one end, and a plunger 18 adapted to expel fluid within the syringe 12 through the outlet tube 16.
Generally the device 10 can be used with one of several embodiments of hose assembies, including any of the hose assembly embodiments described in U.S. Patent No.
4,430,079 and the hose assembly 120 described herein. Like those other hose assemblies, the hose assembly 120 (see Figure 6) has first and second ends 121 and 122, a coupler 125 at its first end 121 for coupling the hose assembly 120 to the syringe 12, and a length of capillary tubing 123 shown coupled to a needle 23 via a Luer-lock fitting 127 at its second end 122 opposite the coupler 121 to facilitate injecting the fluid into a patient's veins or tissues. Alternatively the tubing 123 could be open-ended to facilitate in~ertion of the tubing 123 into a patient's digestive or breathing passages or have attached thereto any shape of head ~ia the Luer-lock fitting 127 or otherwi~e to facilitate distributing fluids to a patient's body. The device 10 includes a support frame 24 comprising spaced fork-like members 26 and 2~ for supporting the coupler 121 and the syringe 12; and spring means 30 for applying uni~orm force agains~ the plunger 18 of the syringe 12 to pre~s it :

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towards the fork-like members 26 and 2~ and cause fluid within the syringe 12 to flow through the hose assembly 120.
The syringe 12 which the dispensing device 10 is adapted to receive is of a conventional type comprising the housing 14 which includes a tubular wall 34 having an open end 35, and an end wall 36 at its end opposite the open end 35 from which projects the outlet tube 16 which defines an outlet opening for the housing 14, and the plunger 18 which has one end portion positioned within and sealing against the inner surface of the tubular wall 34 and an opposite end portion projecting from the open end 35 of the tubular wall 34, and which can have fluid (typically a liquid) within the tubular wall 3~ between the end wall 36 and the plunger 18.
~ he hose assembly 120 used and included in the dispensing device 10 is best seen in Figure 6. Generally, the hose assembly 120, the passageway between the ends 121 and 122 of the hose assembly 120 defined by a capillary tube 123 h~s an volume of less than about 0.25 cubic centimeter and a length of at least 45 centimeters, and perferably in the range of 120 to 170 centimeters and has the coupler 12S at its first end 121. The coupler 125 is adapted for releasably attaching the hose assembly 120 to the housing of the syringe 12 with the outlet opening of the syringe communicating with the passageway through the hose assembly 120 and has an outer periphery shaped so that the coupler 125 will be received in the spaced for~-like members 26 and 28 of the suppo~t frame 24 for the device 10 and will be locked in the fork-like member 26 and 28 when a cover 35 for the device 10 is closed. Both ends of the capillary tube 123 pass into and are bonded within bores of the fitting 127 and the coupler 125 to secure the ends of the capillary tube 123 thereto.
Purging of such a hose assembly 120 in the manner described above proceeds quite rapidly because of the relatively small amount o~ air th~t must be displaced.

~Z~7~9~

The dev.ice 10 includes activating means manually operated by movement of the cover 53 and coupled to the spring means 30 for allowing the syringe 12 and attached hose assembly 120 to be easily inserted in or removed from the device 10 by moving the spring means 30 to a disengaged S position relative to the syringe 12 when the cover 53 is opened, and by moving the spring means 30 to an engaged position against the plunger 18 of the syringe 12 when the cover 53 is closed, and means for securing the syringe 12 and hose assembly in the device 10 when the cover 53 is closed so that they may not be tampered with when the spring means is applying a uniform force to expel fluid from the syringe 12.
The frame 24 includes an elongate bar-like base portion 55 at one end of which is fixed a support member 56 including the spaced fork-like members 26 and 28 which are disposed so that they will position the syringe 12 attached to the coupler 125 received in the fork-like members 26 and 28 over and parallel to the base portion 55. The bar-like baqe portion 55 has upstanding opposed generally L-shaped rails 58 along its edges between which a hollow block 60 is mounted for movement longitudinally of the base portion 55 via four rollers 62 projecting from the edges of the block 60 adjacent the base portion 55. A plate-like slide 64 is also mounted between the rails 58 for sliding movement longitudinally of the base portion 55 between the block 60 and the member 56~ A spring 66 of the type having the ~ registered tradename "Neg'ator" has a portion 68 coiled ; about a hub 69 rotatably mounted within the block 60 on a shaft 70, and a straight end portion 71 extending from the block 60 to the slide 64 where it is attached by a rivet 72. The "Neg'ator" spring 66 provides a constant force attempting to wrap the entire length of the spring 66 onto its coiled portion 68, and thus provides a constant force biasing the block 60 toward the slide 64.
The cover 53 is a rectangular box-like member o~
rigid transparent plastic material (preferably ' .,,:' ~2~3~
g polysulfone) having an open side disposed adjacent the base portion 55 and having opposite outwardly projecting trunnions 74 on its end opposite the support member 56 which are pivotably mounted between the rails 58 and two pins 76 spaced along each of the rails 58 to afford pivotal movement of the cover 53 from an open position spaced from the base member 55, block 60 and syringe 12 (Figure 5); and a closed position adjacent the base member 55 enclosing the block 60 and the syringe 12 therebetween, and with an edge portion 78 of the cover 53 against the coupler 125 received in the fork-like members 26 and 28 to preclude their removal (Figure 2), at which closed position the cover 53 will ke retained by releasable latch means later to be explained. Parallel links 80 are pivotably mounted at their ends between the cover 53 and the slide 64, and are sized and disposed so that moving the cover 53 to its open position (Figure 5) will move the slide 64 and block 60 to a position sufficiently spaced from the fork-like members 26 and 28 that the metering assembly ~0 and attached syringe 12 may be inserted in or removed therefrom; and that moving the cover 53 to its closed position (Figure 2) will move the slide 64 adjacent the support member 56 so that when the syringe 12 and attached coupler 125 are supported from the fork-like members 26 and 28, the block 60 will engage the plunger 18 on the syringe 12 during such movement with the end of the plunger received in a centering pocket 81 in the adjacent face of the block 60. Such engagement will cause the slide 64 to separate from the block 60 in opposition to the spring 66 so that while the cover 53 is closed, the spring 66 will apply a constant ~orce against the plunger 18. Also while the cover 53 is closed, the edge portion 78 rests transversely against the co~pler 125 and precludes its removal from between the fork-like members 26 and 28.
The means for releasably latching the cover 53 in its closed position comprises transverse matinq hook-like lips 8~ and 86, one of which lips 8~ is a part ~Z7~2 o-f the cover 53 adjacent its edge portion 78, and the other of which lips is a part of the fork-like member 26 adjacent its distal end; the spring 66; and a spacing between the pins 76 that allows limited longitudinal rnovement of the cover 53 relative to the base portion 55 of the frame 24. When the cover 53 is being moved to its closed position and after the block 60 engages the plunger 18 of the syringe 12, the force applied by the spring 66 between the separated block 60 and slide 64 via the links 80 will press the trunnions 74 on the cover 53 against the pins 76 oppposite the support member 56. As the cover 53 approaches its closed position, cam surfaces on the lips 84 and ~6 engage to move the center portion of the cover 53 toward the support member 56 and allow the hook-like lips 84 and 86 to pass each other, whereupon the spring 66 again moves the center portion of the cover 53 away from the support member 56 to engage the lips 84 and 86 as the cover 53 reaches its fully closed position. Opening the cover 53 then requires sliding it longitudinally toward the support member 56 against the bias o~ the spring 66 to disengage the lips 84 and 86 before the cover can be pivoted to its open position, which opening operation is not apparent from a casual inspection of the closed cover 53 and could deter unauthori~ed deactivation o~ the device 10. Alternately the means for latching the cover 53 in its closed position could be a more conventional self-latching push button release latch between the cover 53 and base portion 55.
~s an example of the use of the fluid dispensing device 10, a person first fills the syringe 12 with a fluid to be dispensed. Next he attaches the hose assembly 120 to the syringe 12, and manually activates the syringe 12 so that fluid ~lows rapidly through the hose assembly and purges air from it. Next the user presses the coupler 125 between the fork-like member~ 26 and 28 with the ~yringe 12 projecting over the base portion S5. The user then couples the part of the ~itting 12~ on the hose assembly 120 with ., ~ Z~3~

the part on the needle 23 or a cannula (not shown) which he has previously inserted in a patient's vein or tissues, and moves the cover 53 toward its closed position so that the cover 53 via the links 80, slide 64, and spring 66 moves the block 60 into engagement with the plunger 18 on the syringe 12, after which the slide 64 is separated from the block 60 so that the spring 66 will apply a force against the plunger 18. Further movement of the cover 53 to its closed position will cause the lips 84 and 86 on the cover 53 and fork-like members 26 to cam past each other whereupon the spring 66 will maintain the lips 84 and 86 in engagement to latch the cover 53 closed. In this condi-tion, the "Neg'ator" spring 66 will continue to apply a uniform force to cause fluid to flow at a slow uniform rate from the syringe 12 through the hose assembly 120 and needle 23 or cannula into the patient. During this time the device 10 can be positioned in any attitude or carried on the patient to afford ambulation without affecting the fluid dispensing rate. Also tampering with the syringe 12 or hose assembly 120 while the fluid is being dispensed is precluded since the syringe 12 is enclosed by the cover 53, and the coupler 125 is locked between the fork-like members 26 and 2~ by the edge portion 78 of the cover, and anyone attempting to gain access to the syringe 12 or to remove the coupler 125 will have to open the cover 53, thereby deactivating the device 10.
The present invention and its use have been explained with respect to one general type of medical use.
The device may, however, be used in ways other than that indicated both for medical or other uses. For example, one or more of the devices 10 may be used to dispense fluids into a standard intravenous administration set. Also, the fluid dispensing device 10 may be used in industrial application3 such as to introduce chemicals such as a catalyst into fluids moving through a continuou~ proce6s, or for othe~ uses where a s~all continuous supply of fluids is needed. Thus the scope of the invention should not be -12- ~2~73~
limited by either the structure or use of the embodiment described herein, but should be determined only by the scope of the dependent claims.

Claims (7)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A fluid dispensing device adapted for engaging a fluid-filled syringe to dispense fluid from the syringe at a slow, steady rate of less than 60 cubic centimeters per hour, said syringe being of the type comprising an elongate housing including a tubular wall having an open end and an end wall having an outlet opening at the end of the tubular wall opposite its open end, and a plunger having one end portion positioned within and sealing against the inner surface of said tubular wall and an opposite end portion projecting from the open end of said tubular wall, with the fluid being within said tubular wall between said end wall and said plunger, said device comprising:
a hose assembly having first and second ends and comprising a capillary tube defining a passageway between said ends, said capillary tube having a volume of less than about 0.25 cubic centimeter and a length of at least about 45 centimeters, and said hose assembly further including a coupler at said first end adapted for releasably attaching said for the capillary tubing to the housing of a said syringe with the outlet opening of the syringe communicating with said passageway;
a frame comprising support means adapted for engaging and supporting said coupler;
spring means adapted for applying a uniform force against the plunger of the syringe to cause fluid within said syringe to flow through said hose assembly;
and activating means for moving said spring means between a disengaged position spaced from the plunger of a said syringe attached to said coupler to afford insertion or removal of the syringe and said hose assembly, and an engaged position engaged with said plunger to apply said uniform force, said activating means including securing means for securing the syringe and the coupler of said hose assembly in said support means when said activating means positions said spring means in said engaged position.
2. A fluid dispensing device according to claim 1 wherein said capillary tube is over 120 centimeters long.
3. A fluid dispensing device according to claim 1 wherein said is in the range of 120 to 150 centimeters long.
4. A fluid dispensing device according to claim 1 wherein:
said support frame includes an elongate portion extending away from said support means;
said support means are adapted to position a said syringe attached to said coupler over said elongate portion;
said spring means comprises a block mounted for movement along said elongate portion and having a surface adjacent said support means adapted to engage the plunger in a said syringe and a slide slideably mounted between said block and said support means for movement along said elongate portion with said spring means being coupled between said block and said slide for applying a constant force biasing said block toward said support means upon separation of said slide and said block: and said activating means comprises a cover adapted to enclose said block and a said syringe engaged with said coupler over said elongate portion said cover having one end pivotably mounted at the end of said elongate portion opposite said support means and being pivotable between an open position spaced from said elongate portion to afford insertion and removal of said coupler and a said syringe attached thereto and a closed position enclosing said block and the syringe with a portion of said cover providing said securing means, links coupled between said cover and said slide for moving said slide and block to a position spaced from the syringe when said cover is in its open position, and for moving said block into engagement with said syringe to separate said slide from said block and apply said uniform force upon movement of said cover to its closed position, and means for releasably latching said cover in its closed position.
5. A hose assembly adapted for use with a fluid dispensing device which applies a generally constant pressure to dispense fluid throught the hose assembly, said hose assembly comprising a capillary tube having first and second ends and defining a through passageway between said ends, said capillary tube having a volume of less than about 0.25 cubic centimeter and a length of at least 45 centimeters; and said hose assembly further including a coupler at said first end adapted for releasably attaching said hose assembly to a said device with an outlet opening of the device communicating with said through passageway.
6. A hose assembly according to claim 5 wherein said capillary tube is over 120 centimeters long.
7. A hose assembly according to claim 5 wherein said capillary tube is in the range of 120 to 150 centimeters long.
CA000471640A 1984-02-07 1985-01-08 Long capillary tube hose assembly for fluid dispensing device Expired CA1227392A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US577,757 1984-02-07
US06/577,757 US4597754A (en) 1978-11-08 1984-02-07 Long capillary tube hose assembly for fluid dispensing device

Publications (1)

Publication Number Publication Date
CA1227392A true CA1227392A (en) 1987-09-29

Family

ID=24310026

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000471640A Expired CA1227392A (en) 1984-02-07 1985-01-08 Long capillary tube hose assembly for fluid dispensing device

Country Status (1)

Country Link
CA (1) CA1227392A (en)

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