NZ626297B2 - A manually operated medical pump - Google Patents
A manually operated medical pump Download PDFInfo
- Publication number
- NZ626297B2 NZ626297B2 NZ626297A NZ62629712A NZ626297B2 NZ 626297 B2 NZ626297 B2 NZ 626297B2 NZ 626297 A NZ626297 A NZ 626297A NZ 62629712 A NZ62629712 A NZ 62629712A NZ 626297 B2 NZ626297 B2 NZ 626297B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- pump
- fluid
- inlet
- flow pathway
- outlet
- Prior art date
Links
- 239000012530 fluid Substances 0.000 claims abstract description 40
- 238000005086 pumping Methods 0.000 claims abstract description 30
- 230000037361 pathway Effects 0.000 claims abstract description 23
- 230000015572 biosynthetic process Effects 0.000 claims description 8
- 238000005755 formation reaction Methods 0.000 claims description 8
- 238000011144 upstream manufacturing Methods 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 description 6
- 210000002445 Nipples Anatomy 0.000 description 5
- 210000004369 Blood Anatomy 0.000 description 3
- 239000008280 blood Substances 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 230000000717 retained Effects 0.000 description 3
- 230000005484 gravity Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000006011 modification reaction Methods 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 238000001356 surgical procedure Methods 0.000 description 2
- 210000000988 Bone and Bones Anatomy 0.000 description 1
- 230000037250 Clearance Effects 0.000 description 1
- 230000001070 adhesive Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 230000003190 augmentative Effects 0.000 description 1
- 230000035512 clearance Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
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
- A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
- A61M1/80—Suction pumps
- A61M1/82—Membrane pumps, e.g. bulbs
-
- 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
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M2005/1401—Functional features
- A61M2005/1405—Patient controlled analgesia [PCA]
-
- 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
- A61M2205/00—General characteristics of the apparatus
- A61M2205/07—General characteristics of the apparatus having air pumping means
- A61M2205/071—General characteristics of the apparatus having air pumping means hand operated
- A61M2205/075—Bulb type
-
- 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
- A61M3/00—Medical syringes, e.g. enemata; Irrigators
- A61M3/02—Enemata; Irrigators
- A61M3/0233—Enemata; Irrigators characterised by liquid supply means, e.g. from pressurised reservoirs
- A61M3/0254—Enemata; Irrigators characterised by liquid supply means, e.g. from pressurised reservoirs the liquid being pumped
- A61M3/0262—Enemata; Irrigators characterised by liquid supply means, e.g. from pressurised reservoirs the liquid being pumped manually, e.g. by squeezing a bulb
-
- 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
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/142—Pressure infusion, e.g. using pumps
- A61M5/14212—Pumping with an aspiration and an expulsion action
- A61M5/1424—Manually operated pumps
-
- 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
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
- A61M5/16877—Adjusting flow; Devices for setting a flow rate
- A61M5/16881—Regulating valves
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04B—POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
- F04B43/00—Machines, pumps, or pumping installations having flexible working members
- F04B43/08—Machines, pumps, or pumping installations having flexible working members having tubular flexible members
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04B—POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
- F04B9/00—Piston machines or pumps characterised by the driving or driven means to or from their working members
- F04B9/14—Pumps characterised by muscle-power operation
Abstract
Disclosed is a hand operated medical pump. The medical pump includes at least one fluid inlet (120, 140), at least one fluid outlet, a flexible pump bulb (340), at least one directional valve (356, 366) and a bypass flow pathway. The flexible pump bulb defines a pumping chamber which forms at least part of a pumping flow pathway. The at least one directional valve (356, 366) which allows flow of fluid in a direction from the at least one inlet (120, 140) to the at least one outlet, but inhibits flow of fluid in a direction from the at least one outlet to the at least one inlet (120, 140). The bypass flow pathway from the at least one inlet (120, 140) to the at least one outlet bypasses the at least one directional valve (356, 366). The bypass flow pathway extends through the pump bulb (340). part of a pumping flow pathway. The at least one directional valve (356, 366) which allows flow of fluid in a direction from the at least one inlet (120, 140) to the at least one outlet, but inhibits flow of fluid in a direction from the at least one outlet to the at least one inlet (120, 140). The bypass flow pathway from the at least one inlet (120, 140) to the at least one outlet bypasses the at least one directional valve (356, 366). The bypass flow pathway extends through the pump bulb (340).
Description
A MANUALLY OPERATED MEDICAL PUMP
Technical Field
The invention relates to pumps and more particularly to hand operated
pumps for use in medical applications. The invention has been developed primarily for
use as in arthroscopic surgery and will be described hereinafter with reference to this
application. However, it will be appreciated that the invention is not limited to this
particular use. Embodiments of the invention are also suitable for pumping blood and
other fluids in medical applications.
Background to the Invention
During arthroscopic surgery a steady flow of sterile saline fluid is applied to a
region being operated on to clear the operative field of blood and bone debris. From
time to time, it is desirable to apply a large volume bolus of fluid to the operative field
to, for example, expand the joint being operated on, or to clear stubborn debris.
An arrangement described in WO2004/023987 utilises two manually operated
pump bodies. Both pumps can supply a slow steady flow of fluid held in overhead
multiple fluid reservoirs by the action of gravity. However, in order to provide a high
volume flow it is necessary to pump each pump sequentially. This operation requires
two free hands and therefore cannot easily be carried out by a surgeon during an
operation.
An arrangement described in US5,507,707 utilises one manually operated
pump body. A short length of tubing bypasses the pump body to provide a continuous
trickle of flow which can be augmented by operating the pump. However, in order to
operate the pump, the surgeon must carefully insert his fingers between the bypass
tubing and the pump body and take care not to disrupt the bypass tubing. The surgeon
therefore must divert their eyes from the operative filed in order to operate the pump
and must take care when operating the pump not to accidentally disrupt the bypass
tubing.
There remains a need for improved pumping devices which are able to provide
both a continuous steady flow of fluid and can provide an increased flow of fluid on
demand by manual operation of the pumping device.
Summary of the Invention
In a first aspect the present invention provides a hand operated medical pump
including: at least one fluid inlet; at least one fluid outlet; a flexible pump bulb defining
a pumping chamber which forms at least part of a pumping flow pathway; at least one
directional valve which allows flow of fluid in a direction from the at least one inlet to
the at least one outlet, but inhibits flow of fluid in a direction from the at least one outlet
to the at least one inlet; and a bypass flow pathway from the at least one inlet to the at
least one outlet which bypasses the at least one directional valve; and and wherein the
bypass flow pathway extends through the pump bulb.
At least a portion of the bypass flow pathway may be formed by a tube which
is at least partially located within the pump bulb.
The pump may include two fluid inlets, one of which is associated with the
bypass flow pathway.
The pump may include two directional valves, each located respectively
upstream and downstream of the pumping chamber.
The pumping flow pathway and the bypass flow pathway may discharge into a
common output chamber.
The pump bulb may be transparent.
The at least one directional valve may include a flap formation.
The flap formation may be embodied in a flexible washer.
Brief Description of the Drawings
Embodiments of the present invention will now be described, by way of
example only, with reference to the accompanying drawings, in which:
is a side view of a pump;
is cross sectional plan view of the pump depicted in taken along
line A-A;
is an enlarged partial cross sectional plan view of the pump depicted in
taken along line A-A;
is a cross sectional view of an input hub and insert;
is a cross sectional view of an output hub and insert;
is an end view, partially sectioned illustrating an input hub and valve
arrangement; and
is a second embodiment of an output hub and insert illustrating
a concentric discharge.
Detailed Description of the Preferred Embodiment
Referring to through a hand operated pump 100 comprises a
generally cylindrical body 110 having two inlets or nipples and one outlet nozzle. A
bypass inlet 120 receives a first fluid supply 130 and a pumping inlet 140 (as shown in
and receives a second fluid supply 150. The pump 100 discharges
through a single discharge nozzle 160.
The fluid supplies are typically provided in the form of suspended bags of fluid
which are connected to the inlets by way of PVC tubes in a conventional manner. The
fluid may be a saline solution, blood, or other fluid or combination of fluids which may
vary according to the particular application that the pump is to be used for.
Inlets 120, 140 can attach to tubes of at least two sizes depending upon the
applciation at hand. A larger diameter tube fits about the outside of inlets 120, 140. A
smaller diameter tube can be push fitted into inlets 120, 140.
Referring to the body of the pump 100 is built around two similar hubs,
being an inlet hub 310 and a discharge hub 315. Each hub, 310 and 315, has a generally
cylindrical collar for retaining an end cap. The inlet cap 311 is retained, attached to and
sealed against the inlet hub collar 312. The discharge cap 316 is attached to and sealed
against the discharge hub collar 317.
The two hubs, 310 and 315, are interconnected in two ways. A soft PVC (or
rigid) bypass tube 320 extends between the two hubs by affixing to a first inwardly
directed bypass nozzle 322 associated with the inlet hub 310 and a second bypass
nozzle 324 that extends inwardly from the discharge hub 315. The bypass tube 320 may
be fitted to the first nozzle 322 and second nozzle 324, for example by way of any one
of the following: a frictional fit, an interference fit, a weldment or an adhesive etc.
Each hub, 310 and 315, also has an inward facing, axially extending and
generally cylindrical sleeve 330 and 335 respectively. The sleeves, 330 and 335,
support opposites ends of a pump jacket (or bulb) 340. In this example embodiment, the
pump jacket (or bulb) is a flexible cylindrical PVC pump jacket. The cylindrical jacket
340 distorts when squeezed to alter (by reducing) the internal volume of the pumping
chamber 342. The pumping chamber 342 is generally cylindrical. When released the
jacket 340 returns to its original shape.
The inlet hub 310 has a central circular web 313 in which is formed one or
more through openings 352 located around the central bypass channel 350. The
openings 352 lead from the intake chamber 354 to the pumping chamber 342. Fluid can
be manually pumped through a pumping flow path of pump device 100. Manually
pumped fluid enters the inlet nozzle 140 and passes through the intake chamber 354.
From the intake chamber 354, fluid flows through the inlet ports 352 and into the
pumping chamber 342. Back flow from the pumping chamber 342 into the intake
chamber 354 is prevented by one or more flap type check valves 356 as will be
explained with reference to FIGs 4-7.
Fluid in the pumping chamber 342 is discharged through the one or more
discharge ports 362 formed in the central membrane of the discharge hub 315. The
discharge ports 362 lead into a discharge chamber 364. The discharge chamber 364 is
defined by circular web 318 of the discharge hub and the discharge end cap 316. Back
flow from the discharge chamber 364 is prevented by one or more check valves 366.
Fluid flow through the pump’s bypass flow path proceeds from the bypass inlet
or nipple 120, through a second bypass inlet nipple 358 that fits into it and is associated
with the inlet hub 310. Flow proceeds through the nozzle’s bypass channel 350, via the
bypass tube 320, flowing through the central opening of the discharge hub’s bypass
channel 360 and into the discharge chamber 364. Fluid from the pumping inlet 140
proceeds into the discharge chamber 364 when the jacket 340 is squeezed by the
operator. The manually pumped and the bypass flows combine in the discharge
chamber 364 and exit through the single discharge nozzle 160.
In preferred embodiments, the generally cylindrical jacket 340 is at least
partially transparent so that the internal contents of the pump 100 may be viewed by the
operator. The bypass tube 320 may also be transparent.
Further embodiments of the invention are depicted in Figures 4-7. As shown in
Figure 4, an input hub 400 comprises an external bypass inlet or nipple 401 and a
pumping inlet or nipple 402. The hub 400 has a cylindrical outer wall or sleeve 403 that
defines, in part, an intake chamber 404. The intake chamber 404 is also defined by the
end wall 405 of the hub and the external face of an intake insert 406. As suggested by
Figures 4 and 6, the intake insert 406 comprises a generally circular web 407 in which
is formed one or more intake openings 408. In this example, the openings 408 are
arranged in a circular array of equally spaced round openings, all generally equidistant
from the longitudinal centre line of the pump 409. In some embodiments, the openings
408 are tapered from a larger diameter toward the intake to a smaller diameter toward
the output side of the pump. In this example, the insert serves as a check valve.
A thin silicone washer 410 has a central opening that fits over and clears the
inwardly directed bypass nozzle 411. The outer diameter 412 of the silicone flapper or
valve element 410 fits within the insert’s cylindrical shoulder 413. The valve element
410 is retained about its central opening by the bypass tube 414. Accordingly, pressure
in the intake chamber 404 is relieved by fluid passing through the openings 408 and
past the valve element 410. When the pressure equilibrates, the valve element 410
returns to its initial shape and position as shown in Figure 4. The pump jacket 415 is
attached to the exterior of the hub 400 and its axial movement is limited by a shoulder
416 formed on the outer surface of the hub.
As shown in Figure 5, the discharge hub 500 is constructed in accordance with
the teachings related to Figures 4 and 6. In this example, the output hub 500 forms a
single, tapered, discharge nozzle 501. A discharge insert 502 fits within the discharge
hub and abuts an internal shoulder 503. The insert 502 has an array of discharge
openings 504. A silicone washer or valve element 505 prevents backflow and is retained
by a short tubular formation 506 that fits over the tapered discharge outlet 507 formed
integrally with the insert 502. The discharge outlet 507 may be provided with a shoulder
or ridge which serves as a stop to locate and retain the tubular formation 502 on the
discharge outlet. The tubular formaiton may be provided with an internal groove which
cooperates with the ridge. This ensures that silicone washer 505 is not “pinched” by
tubular formation 502 to ensure satisfactory operation of the one way valve
arrangement.
As shown in Figure 7, an alternate embodiment discharges the bypass flow
separately from the flow through the pumping chamber 550. Flow through 20 the
insert’s bypass channel 551 is captured by a preferably tapered conduit 552 that fits
over the bypass insert output nozzle 553. The base end 554 of the conduit 552 serves to
retain or capture the inside diameter 555 of the silicone or other polymeric valve
element 556 and thus replaces the function of the tubular formation 506 shown in
Figure 5. The conduit 552 tapers to a smaller diameter 557 that can exit the discharge
hub’s output nozzle 501 with enough clearance 558 between the outside diameter of the
conduit 557 and inside diameter of the nozzle 501 to accommodate the flow from the
pumping chamber 550. Accordingly, the pump output comprises concentric flow lines
being the larger one 559 for carrying the output of the pumping chamber and the
smaller one, within it and preferably concentrically for 557 carrying the bypass flow.
The purpose of the arrangement of concentric or otherwise separate outputs is to
prevent backflow up the bypass line.
It will be appreciated from the above teachings that the thin, low threshold
flexible silicone check valve elements allow flow through the pump even when the
pump is not being manually or otherwise activated. The design incorporates no valve
elements in the bypass flow path which allows a continuous flow of liquid under the
action of gravity from the supply of fluid.
In some embodiments, the two inlets may be consolidated into a single inlet
which opens into an inlet chamber and the pumping flow pathway and the bypass flow
pathway share this common inlet chamber.
Embodiments of the invention therefore provide a manually operated pump
that provides both manually pressurized fluid as well as a continuous flow of fluid
through a single pumping device that can be easily operated with one hand. The bypass
flow path is protected within the pump bulb and cannot be accidentally disrupted or
dislodged during manual pumping operations.
It will be appreciated that an embodiment of the invention can consist
essentially of features disclosed herein. Alternatively, an embodiment of the invention
can consist of features disclosed herein. The invention illustratively disclosed herein
suitably may be practiced in the absence of any element which is not specifically
disclosed herein.
Reference throughout this specification to “one embodiment” or “an
embodiment” means that a particular feature, structure or characteristic
described in connection with the embodiment is included in at least one
embodiment of the present invention. Thus, appearances of the phrases “in
one embodiment” or “in an embodiment” in various places throughout this
specification are not necessarily all referring to the same embodiment, but
may. Furthermore, the particular features, structures or characteristics may be combined
in any suitable manner, as would be apparent to one of ordinary skill in the art from this
disclosure, in one or more embodiments.
As used herein, unless otherwise specified the use of the ordinal adjectives
“first”, “second”, “third”, etc., to describe a common object, merely indicate that
different instances of like objects are being referred to, and are not intended to imply
that the objects so described must be in a given sequence, either temporally, spatially, in
ranking, or in any other manner.
As used herein, unless otherwise specified the use of terms “horizontal”,
“vertical”, “left”, “right”, “up” and “down”, as well as adjectival and adverbial
derivatives thereof (e.g., “horizontally”, “rightwardly”, "upwardly”, etc.), simply refer
to the orientation of the illustrated structure as the particular drawing figure faces the
reader, or with reference to the orientation of the structure during nominal use, as
appropriate. Similarly, the terms “inwardly” and “outwardly” generally refer to the
orientation of a surface relative to its axis of elongation, or axis of rotation, as
appropriate.
Similarly it should be appreciated that in the above description of exemplary
embodiments of the invention, various features of the invention are sometimes grouped
together in a single embodiment, figure, or description thereof for the purpose of
streamlining the disclosure and aiding in the understanding of one or more of the
various inventive aspects. This method of disclosure, however, is not to be interpreted
as reflecting an intention that the claimed invention requires more features than are
expressly recited in each claim. Rather, as the following claims reflect, inventive
aspects lie in less than all features of a single foregoing disclosed embodiment. Thus,
the claims following the Detailed Description are hereby expressly incorporated into
this Detailed Description, with each claim standing on its own as a separate
embodiment of this invention.
Furthermore, while some embodiments described herein include some but not
other features included in other embodiments, combinations of features of different
embodiments are meant to be within the scope of the invention, and form different
embodiments, as would be understood by those in the art.
In the description provided herein, numerous specific details are set forth.
However, it is understood that embodiments of the invention may be practiced without
these specific details. In other instances, well-known methods, structures and techniques
have not been shown in detail in order not to obscure an understanding of this
description.
Thus, while there has been described what are believed to be the preferred
embodiments of the invention, those skilled in the art will recognize that other and
further modifications may be made thereto without departing from the spirit of the
invention, and it is intended to claim all such changes and modifications as fall within
the scope of the invention. For example, any formulas given above are merely
representative of procedures that may be used. Functionality may be added or deleted
from the block diagrams and operations may be interchanged among functional blocks.
Steps may be added or deleted to methods described within the scope of the present
invention.
Any reference to prior art contained herein is not to be taken as an admission
that the information is common general knowledge, unless otherwise indicated.
Finally, it is to be appreciated that various alterations or additions may be made
to the parts previously described without departing from the spirit or ambit of the
present invention.
Claims (8)
1. A hand operated medical pump including: at least one fluid inlet; at least one fluid outlet; a flexible pump bulb defining a pumping chamber which forms at least part of a pumping flow pathway; at least one directional valve which allows flow of fluid in a direction from the at least one inlet to the at least one outlet, but inhibits flow of fluid in a direction from the at least one outlet to the at least one inlet; and a bypass flow pathway from the at least one inlet to the at least one outlet which bypasses the at least one directional valve; and wherein the bypass flow pathway extends through the pump bulb.
2. A pump according to claim 1 wherein at least a portion of the bypass flow pathway is formed by a tube which is at least partially located within the pump bulb.
3. A pump according to either of claim 1 or claim 2 which includes two fluid inlets, one of which is associated with the bypass flow pathway.
4. A pump according to any preceding claim which includes two directional valves, each located respectively upstream and downstream of the pumping chamber.
5. A pump according to any preceding claim wherein the pumping flow pathway and the bypass flow pathway discharge into a common output chamber.
6. A pump according to any preceding claim wherein the pump bulb is transparent.
7. A pump according to any preceding claim wherein the at least one directional valve includes a flap formation.
8. A pump according to claim 7 wherein the flap formation is embodied in a flexible washer.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2012900028 | 2012-01-04 | ||
AU2012900028A AU2012900028A0 (en) | 2012-01-04 | Arthroscopic Irrigation Pump | |
AU2012903117A AU2012903117A0 (en) | 2012-07-23 | A manually operated medical pump | |
AU2012903117 | 2012-07-23 | ||
PCT/AU2012/001557 WO2013102236A1 (en) | 2012-01-04 | 2012-12-19 | A manually operated medical pump |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ626297A NZ626297A (en) | 2015-03-27 |
NZ626297B2 true NZ626297B2 (en) | 2015-06-30 |
Family
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