NZ607789B2 - Sterilization and humidification apparatus and incubator - Google Patents
Sterilization and humidification apparatus and incubator Download PDFInfo
- Publication number
- NZ607789B2 NZ607789B2 NZ607789A NZ60778913A NZ607789B2 NZ 607789 B2 NZ607789 B2 NZ 607789B2 NZ 607789 A NZ607789 A NZ 607789A NZ 60778913 A NZ60778913 A NZ 60778913A NZ 607789 B2 NZ607789 B2 NZ 607789B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- sterilization
- humidification
- chamber
- humidification apparatus
- gas
- Prior art date
Links
- 230000001954 sterilising Effects 0.000 title claims abstract description 113
- 238000004659 sterilization and disinfection Methods 0.000 title claims abstract description 113
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 76
- 238000010438 heat treatment Methods 0.000 claims abstract description 43
- 239000007788 liquid Substances 0.000 claims abstract description 34
- 239000000919 ceramic Substances 0.000 claims abstract description 14
- 238000001816 cooling Methods 0.000 claims description 43
- 239000000463 material Substances 0.000 claims description 19
- 229910052709 silver Inorganic materials 0.000 claims description 10
- 239000004332 silver Substances 0.000 claims description 10
- -1 polypropylene Polymers 0.000 claims description 5
- 239000011148 porous material Substances 0.000 claims description 5
- 230000001276 controlling effect Effects 0.000 claims description 4
- 238000001914 filtration Methods 0.000 claims description 4
- 238000011144 upstream manufacturing Methods 0.000 claims description 4
- 210000001736 Capillaries Anatomy 0.000 claims description 3
- 239000004743 Polypropylene Substances 0.000 claims description 3
- 229920001155 polypropylene Polymers 0.000 claims description 3
- 229910052904 quartz Inorganic materials 0.000 claims description 3
- 239000010453 quartz Substances 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- 229920005439 Perspex® Polymers 0.000 claims description 2
- 239000004698 Polyethylene (PE) Substances 0.000 claims description 2
- 239000004411 aluminium Substances 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 238000004891 communication Methods 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
- 239000011152 fibreglass Substances 0.000 claims description 2
- 239000011521 glass Substances 0.000 claims description 2
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920000573 polyethylene Polymers 0.000 claims description 2
- 239000004926 polymethyl methacrylate Substances 0.000 claims description 2
- 229910001220 stainless steel Inorganic materials 0.000 claims description 2
- 239000010935 stainless steel Substances 0.000 claims description 2
- 239000012530 fluid Substances 0.000 claims 2
- 230000001419 dependent Effects 0.000 claims 1
- 230000000241 respiratory Effects 0.000 abstract description 2
- 230000029058 respiratory gaseous exchange Effects 0.000 abstract description 2
- 239000000758 substrate Substances 0.000 abstract 2
- 238000009423 ventilation Methods 0.000 abstract 1
- 239000003570 air Substances 0.000 description 129
- 238000005259 measurement Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000000356 contaminant Substances 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 238000011045 prefiltration Methods 0.000 description 3
- 230000000844 anti-bacterial Effects 0.000 description 2
- 230000001105 regulatory Effects 0.000 description 2
- VREFGVBLTWBCJP-UHFFFAOYSA-N Alprazolam Chemical compound C12=CC(Cl)=CC=C2N2C(C)=NN=C2CN=C1C1=CC=CC=C1 VREFGVBLTWBCJP-UHFFFAOYSA-N 0.000 description 1
- 235000003197 Byrsonima crassifolia Nutrition 0.000 description 1
- 240000001546 Byrsonima crassifolia Species 0.000 description 1
- 210000003414 Extremities Anatomy 0.000 description 1
- 206010025482 Malaise Diseases 0.000 description 1
- 241000513347 Pittosporum tenuifolium Species 0.000 description 1
- 206010036590 Premature baby Diseases 0.000 description 1
- 229940035295 Ting Drugs 0.000 description 1
- 210000002700 Urine Anatomy 0.000 description 1
- 210000002268 Wool Anatomy 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 230000000845 anti-microbial Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 230000003750 conditioning Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000001351 cycling Effects 0.000 description 1
- 230000003247 decreasing Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000000813 microbial Effects 0.000 description 1
- 239000012569 microbial contaminant Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006011 modification reaction Methods 0.000 description 1
- 238000001126 phototherapy Methods 0.000 description 1
- 239000002990 reinforced plastic Substances 0.000 description 1
- 230000035812 respiration Effects 0.000 description 1
- 230000001429 stepping Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 230000002588 toxic Effects 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Abstract
607789 Disclosed is a low cost or simplified sterilization and humidification apparatus used separately or part of an incubator to provide ventilation or for treatment of breathing or respiratory conditions in infants or babies. The apparatus includes a heating chamber, a ceramic filter and a humidification chamber. The heating chamber heats a gas or air to a sterilization temperature to sterilize the gas. The humidification chamber is adapted so that a liquid such as water, which has been filtered by the filter, evaporates from an exposed surface of a wicking substrate into the sterilized gas, causing the sterilized gas to cool, and supplying a humidified gas at a desired temperature. ification chamber. The heating chamber heats a gas or air to a sterilization temperature to sterilize the gas. The humidification chamber is adapted so that a liquid such as water, which has been filtered by the filter, evaporates from an exposed surface of a wicking substrate into the sterilized gas, causing the sterilized gas to cool, and supplying a humidified gas at a desired temperature.
Description
Our Ref: MED039NZ
Patents Form No. 5
PATENTS ACT 1953
Complete After Provisional No. 598597 filed 6 March 2012
TE SPECIFICATION
STERILIZATION AND HUMIDIFICATION APPARATUS AND INCUBATOR
We, Mondiale Technologies Limited, a New Zealand company of 17 Matipo Street, Mt
Eden, Auckland, New Zealand, do hereby declare the invention for which we pray that
a patent may be granted to us, and the method by which it is to be performed, to be
particularly bed in and by the following statement:
STERILIZATION AND HUMIDIFICATION APPARATUS AND INCUBATOR
FIELD OF THE INVENTION
The invention relates to sterilization and humidification apparatuses, in
particular but not exclusively to incubators including sterilization and
fication tuses.
BACKGROUND TO THE INVENTION
ure and unwell babies are often cared for in incubators, which are
designed to keep the baby warm, maintain an here that has a suitable
ty and that is as free of contaminants as possible.
Existing incubators may include systems designed to introduce clean air into the
main chamber of the incubator. Such air should ideally be as free as possible of
particulate and microbial contaminants. In some hospital environments, the
ambient air is already sufficiently clean (due to, for example, air conditioning
systems) such that incubators do not arily need specialised air treatment
equipment. However, in other hospital environments — particularly in
developing countries — the t air has undergone l conditioning,
and therefore the need for specialised air treatment in incubators is of more
importance.
In addition to clean air, existing incubators include systems designed to provide
a suitably humidified environment inside the main chamber of the incubator.
The water used in humidification systems should ideally be as free as possible of
particulate and ial contaminants. In some hospitals — particularly in
developing countries — a clean water source is often not available, and therefore
the need for specialised water treatment in incubators is of more importance.
Current incubators suffer from a number of problems. tors tend to be
made of expensive materials and require regular nance. This serves to
increase the costs and make the incubators less affordable and accessible. This is
particularly the case in developing ies.
Maintenance of existing incubators can also be expensive. In developing
countries there is mes no one who has the expertise
necessary to m
even routine maintenance tasks. This leads to expensive incubators being
unusable because of routine faults and lack of led preventative
maintenance.
As discussed earlier, there are systems available which attempt to maintain a
sterilized environment, but such systems are often expensive, bulky and require
regular servicing or replacement.
It is an object of the invention to e an improved sterilization and
humidification apparatus and/or an improved incubator or at least to provide the
public with a useful choice.
SUMMARY OF THE INVENTION
According to one exemplary embodiment there is provided a sterilization and
humidification apparatus including: a heating chamber for heating a
gas to a first
temperature so as to sterilize the gas; a first filter for ing a liquid; and a
fication and cooling chamber adapted to enable the filtered liquid to
evaporate into the sterilized gas, thereby g the sterilized gas to cool, and
outputting a humidified gas at a desired temperature.
According to another exemplary embodiment there is provided an incubator
including: a ization and humidification apparatus as claimed in any
preceding claim; and an occupancy chamber; wherein the tor is adapted
to cause the humidified gas to flow into the
occupancy chamber.
According to a further exemplary embodiment there is provided an incubator
including: an ncy chamber;a first inlet for receiving an input gas; a
second inlet for receiving an input liquid; and a
porous ceramic filter for filtering
the input liquid; wherein the incubator is configured to evaporate the input
liquid into the input gas after the input liquid has passed through the porous
ceramic filter, thereby producing a humidified gas, which is made to flow into
the occupancy r.
BRIEF PTION OF THE DRAWINGS
The invention will now be described by
way of example only, with reference to
the accompanying drawings, in which:
Figure 1 is a block diagram of a sterilization and humidification
apparatus according to the present invention;
Figure 2 is an isometric view of an assembled sterilization and
fication apparatus;
Figure 3 is a cross section of a gas filter;
Figure 4 is an isometric view of a flow device;
Figure 5 is an exploded view of a heating chamber of the
sterilization and humidification apparatus of Figure 2;
Figure 6a is a cross section of a liquid source and a liquid filter of the
sterilization and humidification apparatus of Figure 2;
Figure 6b is an isometric view of a liquid source and a liquid filter of
the sterilization and fication apparatus of Figure 2;
Figure 7 is an exploded view of a reservoir, wicking members and
humidification and cooling chamber of the sterilization and
humidification apparatus of Figure 2;
Figure 8 is an isometric view of an assembled ization and
humidification apparatus according to another
embodiment;
Figure 9 is an isometric view of a portion of the ization and
humidification apparatus of Figure 8;
Figures 10a and 10b is a cross section of the humidification and cooling
chamber and bypass chamber of the sterilization and
humidification apparatus of Figure 8;
Figure 9 is an exploded view of a portion of the sterilization and
humidification apparatus of Figure 8;
Figure 12 is a block diagram of a controller;
Figure 13 is an isometric view of an incubator; and
Figure 14 is an exploded view of an incubator.
DETAILED DESCRIPTION
Figure 1 is a block diagram of a sterilization and humidification apparatus 1
according to one embodiment. Generally, the sterilization and humidification
apparatus may include a gas source (later referred to as an ’air source’) 2, a gas
filter (later referred to as an ’air ’) 3, a flow device 4 (e.g. a fan), a heating
chamber 5, a humidification and g chamber 6, a liquid source (later
ed to as a ’water ’) 7, a liquid filter (later referred
to as a ’water filter’)
8, a reservoir 9, a wicking member 10 and a controller 11. In some
embodiments, the humidification r 6 may act as a humidification and
cooling chamber.
Figure 2 shows an assembled ization and humidification apparatus 1
according to one embodiment. The figure shows a flow device 4, a heating
chamber 5, a humidification chamber 6, a reservoir 9 and a water source 7.
Other components of the sterilization and humidification apparatus are
obscured. Gas and liquid flow through the sterilization and humidification
apparatus 1 according to the description of each step and component part
outlined below.
Those skilled in the art will appreciate that in some instances it is necessary for
the steps to happen sequentially or in a particular order, and in other instances
the sequence of the step is not al. As will become apparent from the
description, the operation of the sterilization and humidification apparatus
results in the output of a humidified gas 12 (Figure 1), with the tuent gas
and liquid both having been filtered and/or sterilized. In some embodiments, the
sterilization and humidification apparatus may also include a bypass chamber
49 and a mixing chamber 52, resulting in the output of a mixed humidified gas
54, as discussed below.
The sterilization and fication apparatus 1 is connected to a gas source 2.
In a preferred embodiment, the gas is air. There are any number of suitable ways
by which air can be introduced into an apparatus. By way of example, air from
the ambient environment may enter the sterilization and humidification
apparatus through a basic inlet; or a pressurised air source may be connected to
the sterilization and fication tus by a suitable conduit. Any suitable
fan or similar may be used to introduce air.
The sterilization and humidification apparatus 1 is also connected to a liquid
source 7. In a preferred embodiment, the liquid is water. There are any number
of le ways by which water can be uced into an
apparatus. By way of
example, the water source could be a tank that is manually filled or replaced,
which can be connected to the sterilization and humidification apparatus by a
suitable conduit; or the water source could be a pressurised water source (such
as the water mains) which can be connected to the sterilization and
humidification apparatus by a suitable conduit.
Figure 3 shows an air filter 3. The air, after entering the sterilization and
humidification apparatus, flows through the air filter as indicated by the arrow.
The air filter serves to remove particulate contaminants from the air. It will be
1O appreciated that the air filter should ideally be disposed such that it upts
the entire flow of air through the sterilization and humidification apparatus. in
one embodiment, the air filter is made up of a plurality of filter media 13, 14, 15
ordered tially in the flow of air. In one embodiment, the main filter 14 is
a High Efficiency Particle Arresting (HEPA) filter which has a particle arrestance
of 95—99.7% for 0.3 —O.5 micron particles.
The air filter 3 may include a readily replaceable pre—filter 13 disposed on the air
filter's upstream side. The pre—filter may be y d, washed and
replaced. Such a pre—filter serves to extend the lifespan of the other components
of the air filter 14, 15. The lter may be made of a polypropylene or other
suitable material.
The air filter 3 may also include a filter material 15 impregnated with
nanoparticulate silver on its downstream side. This helps to t the
propagation of microbial contamination on the downstream side of the HEPA
filter 14 (ie contributes to the sterilization of the air).
Figure 4 shows a flow device 4 according to one ment. The flow device
may include a fan (not shown), which draws in air in one direction 16, and
expels air in another direction 17. Such a flow device is configured so as to
ensure the air flows through the sterilization and humidification apparatus at the
desired speed and pressure. As will be described later, the flow device may be
ted to a controller which controls the operation of the flow device,
including the speed of the fan. The flow device may be upstream or
downstream of the air filter 3. In another embodiment, the flow device may be a
pump.
Figure 5 shows an exploded view of a heating chamber according to one
embodiment of the present invention. The heating chamber includes a housing
18, a heater element 19 and a ting bulk material 20, which in Figure 5 is
shown as series of fins 21 embedded radially in a cylindrical base member 22.
The heater element and conducting bulk material are adapted so that the
conducting bulk material dissipates heat from the heater t. The
cylindrical base member may include a hollow core 23 that receives the heater
element inside it.
The heater element 19 may be any suitable device that can be connected to
power source (not shown) and generate heat. In a red embodiment, the
base member 22 and fins 21 are made inately from a conductive
material, such that when the heater element is ed on, heat is conducted
from the heater element, to the base member, and to the fins. The air enters the
heating chamber 5 through an inlet (not shown) adjacent to the flow device. The
air then flows adjacent or near the radial extremities of the fins in an outer
region of the heating chamber between the fins and the inside of the housing 18
(to the left as shown in Figure 5). The air passes around the end of the bulk
material 20, into an inner region between the base member 22 and fins. The air
then flows along the length of the bulk material 20 (to the right as shown in
Figure 5), before exiting the heating chamber through an outlet (not shown).
As will be appreciated by those skilled in the art, the arrangement of the heater
element 19 and conducting bulk material 22 are such as to maximise the
exposure of the air to the conducting bulk material as the air flows through the
heating chamber 5. This increases the effectiveness of the heating of the air in
the heating chamber. Typically, this can be achieved by configuring the heating
chamber with an air flow (ie the course that the air must ) that increases
the re of the air to heat and lengthens the path between the inlet and
outlet. In addition to the conductive bulk material, the g chamber may
also include suitable protrusions to direct the flow of the air
as it passes h
the heating chamber.
Thus, the air will increase in temperature as it passes through the heating
chamber 5. The temperature should be sufficient to sterilize the air. In a
preferred embodiment, the air is heated to 180—200 degrees Celsius. As will be
bed later, the heating chamber may include temperature sensors to ensure
that the air is being heated to a sufficiently high temperature. The heater element
19 may be ted to a controller for control of heating
power.
Figure 6a shows a cross section of a water source 7 and a water filter 8, and
Figure 6b shows an isometric view of the or of the water source 7. The
water source is a tank that can be manually filled through an opening 24.
Disposed inside the water tank is a cylindrical water filter 8. The top of the water
filter is closed so water flows initially into the tank space 24’. Water passes from
the water tank into the water filter, and out an outlet 25. Preferably, the water
filter is a ceramic filter with a porous ceramic body structure. The maximum
pore size of the porous ceramic is preferably 0.1—0.2 microns, and ideally 0.2
microns. In this way, the water that flows our of the water filter and into the
remainder of the sterilization and humidification apparatus is ed water.
In a further embodiment, the porous ceramic of the water filter 8 is impregnated
with nanoparticulate silver. Nanoparticulate silver has antibacterial properties
and ore, as the water passes through the water filter, the water is also
sterilized. In on to, or alternatively to, the nanoparticulate silver, the water
filter may be configured with a hollow core that is filled with silvered quartz
pieces. The dimension of the pieces may be 2—5 mm in diameter. Again, the
silvered quartz pieces have an antibacterial effect on the water that flows
adjacent or near to it, and this causes the water to be steriiized.
Figure 7 shows an exploded view of part of the sterilization and humidification
apparatus 1. A reservoir 9 is obscured — being the region below the dotted line
29. Figure 7 also shows wicking s 10 (three of which are ted), a
humidification and cooling chamber 6, and a cap 29a which together are
configured as a single unit. Figure 7 also shows a portion of the housing 18 from
Figure 5.
The reservoir 9 includes an inlet 26 that is ly ted to the outlet 25
from the water source 7 / water filter 8. The reservoir 9 is configured so that it
has a continuous supply of water. In this instance, the water source 7 described
earlier is disposed higher than the reservoir in such a way that provided the
water tank is kept sufficiently full, the amount of water in the reservoir is always
sufficient.
The humidification and cooling chamber 6 es an inlet 27 that is
connected to the outlet from the heating chamber. h this inlet, the heated
air from the g chamber enters the humidification and cooling chamber. As
will be bed in more detail below, as the heated air passes through the
humidification and cooling chamber it is humidified and cooled. The
humidification and cooling chamber also includes an outlet 28, from which the
1O humidified air exits the sterilization and humidification tus.
Between the oir and the humidification and cooling chamber, there is a
barrier (as shown by the dotted line 29) through which the wicking members 10
are positioned. The barrier and wicking members are arranged such that there is
no direct interface between the water in the reservoir 9 and the air in the
humidification and cooling chamber 6. The wicking members are configured
such that a portion of each wicking member is always in contact with the water
in the reservoir and a portion of each wicking member is always in contact with
the air in the humidification and cooling chamber.
Each wicking member 10 is adapted to draw water from the oir 9 by
capillary action, and thus the water is able to traverse the barrier 29 between the
reservoir and the humidification and cooling chamber 6. The wicking members
may be disposed in a vertical arrangement with the reservoir on the bottom, and
thus the capillary action acts t gravitational force.
In one embodiment, the wicking members 10 are made from a porous ceramic
and act as a filter in addition to a wick. The maximum pore size of the porous
ceramic is preferably 0.1—0.2 microns, and ideally 0.2 microns. in this way, the
water that flows from the reservoir to the humidification and cooling chamber is
filtered.
In a further embodiment, the porous ceramic of the wicking members 10 is
impregnated with nanoparticulate silver. As the water passes through the
g members, the water is also sterilized.
The portion of the g member 10 in t with the heated air acts as an
evaporative surface, from which the water evaporates into the heated air. The
positioning of the wicking members in the humidification and cooling chamber
6 is such as to increase the exposure of the heated air to the evaporative surface
of the wicking members. In one embodiment, the wicking s define the
boundary of a meandering course in the humidification and cooling r
through which the heated air flows. The cap 29a helps to maintain the wicking
members in on (with shaped regions 29b receiving the tops of the wicking
members 10) and also seals the top of the humidification and cooling chamber.
Once the water has flowed to the evaporative e, it then evaporates into the
heated air. As the water evaporates into the heated air, the heated air becomes
humidified. Further, the heated air cools as it loses energy due to the latent heat
of vaporization needed to change the phase of the water from a liquid to a gas
(i.e. steam or water vapour).
In an alternative embodiment that will be described below, the proportion of the
heated air that passes through the fication and cooling r may be
adjusted to control the temperature and humidity of the humidified air exiting
the humidification and cooling chamber. As will also be described below,
ing the temperature of the heating chamber and the speed of the flow
device may also allow the temperature and humidity of the fied air to be
controlled.
Figure 8 shows another embodiment of a sterilization and humidification
1O apparatus 1’. In this ment, the proportion of heated air that passes
through the humidification and cooling chamber can be controlled, which in
turn allows the temperature and humidity of the humidified air to be controlled.
As with the embodiment described above in relation to Figures 2—7, the
sterilization and humidification apparatus 1’ of Figure 8 includes an air filter 3’,
a flow device 4’, a heating chamber 5’, a humidification and cooling chamber
6’, a water source 7’, a water filter 8’, a reservoir 9’ and wicking members 10’
(two of which have been indicated). The humidification and cooling chamber
may include a transparent top window 47 to enable easy tion. The flow
device causes air to flow through the air filter to filter contaminates. The air then
flows h the heating chamber, heating to a sufficient temperature to
sterilize the air, before it flows into the humidification and cooling chamber.
Water from the water source is filtered and/or sterilized before collecting in the
reservoir. The wicking members cause the water from the reservoir to be drawn
up into the fication and cooling chamber. The wicking members may
filter and/or sterilize the water. The heated air causes the water to evaporate
from the wicking s; this humidifies and cools the heated air to produce
humidified air, which then exits the humidification and cooling chamber from a
humidification and cooling chamber outlet 48. Those d in the art will
appreciate how the various features described in relation to the apparatus of
Figures 2—7 can be modified to apply to the apparatus of Figures 8 and 9.
However, unlike the apparatus of Figures 2—7, the sterilization and
humidification apparatus of Figure 8 also es a bypass chamber 49,
distribution chamber 50, a distribution adjustment mechanism 51 and a mixing
chamber 52 as shown in Figure 8 and in the partial view of the apparatus in
1O Figure 9. It will be appreciated that the distribution chamber and mixing
chamber are not shown as enclosed s in Figure 9 since parts of the
apparatus have been removed to show the interior more clearly.
The bypass chamber 49 provides an alternative path for a portion of the heated
air flowing out of the heating chamber. Rather than flow through the
humidification and g chamber 6’, some of the heated air may flow
through the bypass chamber. In the bypass chamber, the heated air is not
exposed to any water, and therefore the heated air exits the bypass r
through a bypass chamber outlet 53 with essentially the same temperature and
humidity as when it d the bypass chamber. The heated air that exits
h the bypass outlet then mixes with the humidified air that exits through
the humidification and cooling chamber outlet 48 in the mixing chamber 52.
The mixed humidified air (i.e. humidified and heated air, and heated air), then
exits the apparatus through an apparatus outlet (28’ in Figure 8).
The distribution chamber 50 connects the heating device 5’ to the
humidification and cooling chamber 6’ and the bypass r 49. By adjusting
a suitable bution adjustment mechanism 51, it is possible to control what
proportion of heated air flows into the humidification and cooling chamber and
what proportion of the heated air flows into the bypass chamber. It will be
appreciated that by increasing the proportion of heated air that flows into the
bypass chamber, the mixed humidified air will have a higher temperature and
lower humidity. Conversely, by decreasing the proportion of heated air that
flows into the bypass r, the mixed humidified air will have a lower
temperature and higher humidity. Thus, by adjusting the distribution adjustment
mechanism the temperature and humidity of the mixed humidified air can be
regulated. In one embodiment, after the apparatus is operating at a set air speed
and rate of heating, the temperature and humidity of the humidified air can be
further regulated by adjusting the bution adjustment ism.
In Figure 9, the distribution adjustment mechanism 51 is shown as an inlet
sliding valve 55 connected to a suitable drive mechanism 56. The inlet sliding
valve is configured to slide between: a first position that fully seals the
humidification and cooling chamber inlet 27', a second position that fully seals
the bypass r inlet 57; and a range of ons between the first position
and second position where both inlets are partially open. The inlet g valve
is therefore able to fully or partially block the passage of the heated air into and
through each of the humidification and cooling r 6’ and the bypass
chamber 49. With the inlet sliding valve in the first position, all of the heated air
flows through the bypass chamber, and with the sliding valve in the second
position, all of the heated air flows through the humidification and cooling
chamber.
In one embodiment, the distribution adjustment mechanism 51 may include a
further outlet sliding valve 58 red) that is configured to slide between: a
first position that fully seals the humidification and cooling r outlet 48, a
second position that fully seals the bypass chamber outlet 53; and a range of
positions between the first position and second position where both outlets are
partially open. In a preferred embodiment, the inlet g valve and outlet
sliding valve 55 may be slid between their first and second positions in unison.
The sliding valves may be connected to the same drive mechanism 56.
The benefit of having both an inlet valve 55 and an outlet valve 58 is best shown
by considering an apparatus that only has an inlet sliding valve (as shown in the
cross-section of Figure 10a). If the inlet sliding valve is in the first position, all of
the heated air flows through the bypass r 49. As the heated air passes
through the mixing chamber 52, the venturi effect causes some of the heated air
to flow into and out of the humidification and cooling chamber 6’ via the
fication and cooling chamber outlet 48. This may result in some
humidified air being mixed with the heated air. Conversely, if there is also an
outlet sliding valve 58 (as shown in the cross-section of Figure 10b), there is no
opportunity for the venturi effect to occur, and thus there is no unwanted
increase in ty. This allows a less humid and warmer air to be output. It
will be appreciated how the above reasoning can also apply to the situation
where the sliding valve is in the second position, which allows a more humid
and cooler air to be . Therefore, having two sliding valves allows air with
a greater range of humidity and temperature to be output and with more
precision.
The drive mechanism 56 may be a screw driven stepping motor or a suitable
manually adjustable mechanical drive mechanism. The drive mechanism may
be connected to a controller. The controller may automatically control the drive
mechanism based on data from sensors so that the mixed humidified air has the
desired temperature and humidity. The mechanism may include a rotating
threaded shaft 59 riding in fixed nuts 60 attached to the sliding valve.
Figure 11 shows an ed view of a part of the sterilization and
humidification tus 1’ of Figure 8. The figure shows the heating chamber
5’, the wicking members 10’ (two of which have been ted), humidification
and cooling chamber 6’, bypass chamber 49, lid 29a’ with transparent window
47, and inlet sliding valve 55. The figure shows the wicking members positioned
in a barrier 29’, which prevents there being a direct interface n the
reservoir 9’ and humidification and cooling chamber.
Figure 11 also shows a reservoir 9’, reservoir lid 61 and float 62. The reservoir
extends beneath the fication and cooling chamber 6’ such that the
portion of the wicking members 10’ below the r 29’ are exposed to the
water in the reservoir. The float is adapted to ensure the water level in the
reservoir is sufficient. When the water level falls (due to water being evaporated
in the humidification and cooling chamber), the float will lower. This will open
a valve 63 that connects the reservoir to the water source 7’. Water will flow
from the water source into the reservoir so that water level rises until the float is
at a sufficient level to close the valve.
Figure 12 shows a block m of a controller 11 according to an embodiment
of the present invention. The ller is adapted to control the flow device 4,
the heater element 19, and the distribution adjustment mechanism (via the drive
mechanism 56). The controller is also connected to sensors 30, for detecting
various operating states of the sterilization and humidification apparatus. The
controller includes a central processing unit 31. In one embodiment, the
controller is a digital programmable logic controller.
The controller 11 may control the flow device 4. The controller may control the
flow device’s on and off cycles or the flow device’s speed (that is, where the
flow device can achieve a variable flow speed). The controller may control the
power input into the flow device or some other operating characteristic of the
flow device itself.
Similarly, the controller 11 may control the heater element 19 (and thus the
heating chamber). The ller may control the heater element’s on and off
cycles or the heater element’s power or temperature (that is, where the heater
element can achieve variable heating). The controller may control the power
input into the heater t or some other operating characteristic of the heater
element itself.
The controller 11 may control the drive mechanism 56 (and thus the distribution
adjustment mechanism 51). Where the drive mechanism is a stepper motor
connected to a sliding valve(s), the controller may control the position of the
stepper motor, or may turn the r motor in an riate direction, to
l the position of the sliding valve(s).
One or more s 30 may be positioned so as to take gs of various
ters at appropriate points in the sterilization and humidification
apparatus. Such sensors may be any suitable sensor d for measuring the
particular parameter, and the invention is not limited in this respect. The
measurements could include:
ature of water source;
temperature of air source;
temperature of air at points within the heating chamber;
temperature of the heater element;
temperature of the bulk tive material;
temperature of air at points within the humidification and cooling
r;
temperature of air as it exits the humidification and cooling chamber;
temperature of air at points within the bypass chamber;
temperature of air as it exits the bypass Chamber;
humidity of air source;
humidity of air at points within the g chamber;
humidity of air at points within the humidification and g chamber;
humidity of air as it exits the humidification and cooling chamber; and
speed of air flow throughout the sterilization and humidification
apparatus.
The readings from these sensors are provided as inputs into the controller, and
used by the controller to determine the appropriate operating parameters for the
flow device, the heater element and the drive mechanism. The controller may
adjust the operating parameters such that the humidified air that exits the
sterilization and humidification apparatus has the desired temperature and
desired humidity. In one embodiment these are preferably between 25—38
s Celsius and 30—80% relative humidity.
The controller may also control other operating parameters of the sterilization
and humidification apparatus. The controller may receive input from other
sensors 31 as required, and may control other components 32 associated with
the sterilization and humidification apparatus as required. For example, these
may include:
o a clock for recording the g time of an associated incubator; and
- alarms for alerting to: the temperature and/or humidity falling outside a
desired range; sensor e; and low water in the water tank or water
reservoir.
One or more user input devices 33 may be provided, allowing a user to set
control parameters or otherwise interact with the controller. Control parameters
may be stored in memory within or associated with the controller.
Thus it will be seen that the sterilization and humidification apparatus is adapted
to produce humidified air, with a desired temperature and humidity. In addition,
the prior tion and sterilization of air, and the prior tion and sterilization
of the water, ensures that the humidified air is also filtered and sterilized. Such
sterilized and humidified air may be suitable for any number of applications, in
particular for use in an incubator.
Figure 13 shows an tor ing to an embodiment of the present
ion. The incubator 34 includes an occupancy chamber 35 and a bottom
section 36. The occupancy chamber includes a top wall 37, which may be
hinged or removable enabling access to the interior of the occupancy chamber.
In Figure 13, the top wall is shown in an open position.
In one embodiment of the invention, the occupancy chamber 35 is configured
to receive an occupant, generally a human baby. Babies requiring incubation
are usually neonatal and/or premature babies. The top wall 37 may be
transparent to enable the occupant of the incubator to be visible. To maintain a
healthy environment for the occupant of the incubator it is necessary to provide
a continuous supply of fresh air. If the air is continuously culated or
allowed to stagnate, carbon dioxide and ammonia gas (due to urine es)
within the incubator may increase to toxic levels.
Figure 14 shows an exploded view of the same incubator 34 as that shown in
Figure 13. The incubator includes an ncy r 35, a bottom section
36 and a top wall 37.
The bottom section 36 includes the sterilization and humidification apparatus 1
according to the above description of Figures 2—7. The incubator 34 is
configured such that the output 28 of the sterilization and humidification
apparatus is connected to the occupancy chamber 35 by a suitable conduit.
Those skilled in the art will appreciate that the sterilization and humidification
tus of Figures 8 and 9 may alternatively be used.
The humidified air (or mixed fied air) produced by the sterilization and
humidification apparatus 1 then passes into the occupancy chamber 35 through
an inlet 38. In on embodiment of the invention, this inlet es grills 39 that
may be designed to create a laminar flow effect. The humidified air passes
through the occupancy chamber and is discharged to the ambient environment
via a suitable outlet 40. The position of the inlet and the outlet may be
ured to promote the flow and cycling of the humidified air in the
occupancy chamber. In addition, the geometry of the occupancy chamber may
be arranged to promote the flow of the humidified air through the occupancy
chamber.
In one embodiment of the invention, when the top wall 37 is opened, the
laminar flow of humidified air will continue to pass over the occupant’s head
and torso, acting as an ”air shield”.
The incubator 34 may include a controller (not shown). In a preferred
embodiment, this controller includes, or is one and the same as, the controller
11 described above in relation to the ization and fication apparatus.
Thus, in addition to controlling the operation of the sterilization and
humidification apparatus 1, the controller may control the operation of the
tor more generally.
Referring again to Figure 12, the controller 11 may be connected to further
sensors 41 associated with the incubator. These sensors 41 could include
s for ing the temperature of the nt; the temperature of the
air inside the occupancy chamber; and the humidity of the air inside the
occupancy r. The readings from these sensors are provided as inputs into
the controller, and used by the controller to determine the appropriate operating
parameters for the flow device 4 the heater element 19 and the drive mechanism
56. In a preferred embodiment, the controller controls the sterilization and
humidification apparatus to ensure the temperature and humidity inside the
occupancy chamber are within desired ranges since this provides the best
control of the occupant’s immediate environment. In one embodiment, these are
preferably n 25—38 degrees Celsius and 30—80% ve humidity.
The controller 11 may record measurements from the various monitoring
devices 42. These monitoring s could include devices for monitoring an
occupant’s temperature, pulse or respiration rate. The monitoring devices may
be hard wired or ss.
The incubator may include one or more communication ports configured for
connection to one or more external devices 43. information may be
communicated from the controller to an external device over any suitable
communications link, eg RS—232, USB or a wireless link. Measurements may
include ature inside the incubator, humidity inside the incubator, body
temperature of the incubator occupant, and/or any other desired measurement.
One or more display s 44 may also be provided, for display of operational
parameters, alerts, monitoring information, occupant status information (eg
temperature, humidity, pulse rate readings etc) or any other required
information. A display device may be attached to the side of the incubator.
In one ment, the temperature of the occupancy chamber is set by a user,
the user being able to set the ed ature or temperature range on the
temperature controller.
Referring again to Figure 13, the occupancy chamber 35 may include a base unit
45 that is formed as a separate, portable unit. The occupant may be disposed on
the base unit. This allows the base unit and its occupant to be moved
independently of the remainder of the incubator 34. The base unit may be
provided with carrying handles 46. The base unit may be fitted with a suitable
mattress 47. The mattress may be a removable washable moulded mattress,
and may be constructed of a synthetic fibre and wool blend. The mattress may
be impregnated with nanoparticulate silver and/or gold, which may provide anti-
ial properties.
The base unit 45 allows measurements or tests (eg weighing the baby) to be
med without unduly disturbing the baby. The weight of the unoccupied
base unit is known and can be subtracted from the weight of the base unit and
occupant. Other ements, tests and procedures may also be performed
without removing the baby from the portable base unit (eg x-rays, phototherapy).
The occupancy chamber 35 may have le openings to allow connection of
ary equipment, such as respirators, IV infusion systems, monitoring
equipment and waste systems.
In one embodiment of the invention, the incubator 34 and/or its component
parts are made from light, durable materials that can be d into the
desired components. A preferred material is polypropylene, though a wide
number of suitable materials are available, including polyethylene, Perspex,
polycarbonate, fibreglass, glass, reinforced plastic, carbon fibre, aluminium and
stainless steel.
In one embodiment, at least one interior e of the tor 34, preferably
an interior wall of the occupancy chamber 35 is coated or impregnated with
nanoparticulate silver. This assists with maintaining a relatively sterile chamber
as silver in this form has anti-microbial ties.
Although described with reference to a sterilization and humidification
apparatus, in one embodiment an incubator may include the humidification
device or chamber 6 with or without the heat chamber 5.
Although described in the context of an incubator, the Applicant’s sterilization
and fication apparatus has wider applications, particularly in the medical
field. The sterilization and humidification device could be used in respiratory
humidifiers and/or ventilators or in sterilization systems for medical ments
and the like.
While the present invention has been illustrated by the description of the
embodiments thereof, and while the embodiments have been described in
detail, it is not the intention of the Applicant to restrict or in any way limit the
scope of the appended claims to such detail. Additional advantages and
modifications will readily appear to those skilled in the art. ore, the
invention in its broader aspects is not limited to the specific s,
representative apparatus and methods, and illustrative examples shown and
described. Accordingly, departures may be made from such details t
departure from the spirit or scope of the ant’s general inventive concept.
Claims (60)
1. A sterilization and humidification apparatus ing: i. a heating r for heating a gas to a first temperature so as to sterilize the gas; ii. a first filter for filtering a liquid; and iii. a humidification chamber adapted to enable the filtered liquid to evaporate into the ized gas, thereby g the sterilized gas to cool, and outputting a humidified gas at a desired temperature.
2. The sterilization and humidification heating apparatus as claimed in claim 1, wherein the humidification chamber is a humidification and cooling chamber. 15
3. The sterilization and humidification apparatus as d in claim 1, wherein the humidification chamber includes an ative surface, which brings the filtered liquid into contact with the sterilized gas.
4. The sterilization and humidification apparatus as claimed in claim 3, 20 n the evaporative surface is an exposed surface of a wicking member, which is adapted to draw the filtered liquid from a source to the humidification chamber by means of capillary action.
5. The sterilization and humidification apparatus as claimed in claim 4, 25 wherein the wicking member is, or forms part of, the first filter.
6. The sterilization and fication apparatus as claimed in claim 5, wherein the wicking member is a porous al that filters the .
7. The sterilization and humidification apparatus as claimed in claim 6, wherein the porous material of the wicking member is a porous ceramic with a maximum pore diameter of 0.2 microns.
8. The sterilization and humidification apparatus as claimed in claim 4, wherein the wicking member is adapted to sterilize the liquid.
9. The sterilization and humidification apparatus as claimed in claims 6, wherein the wicking member is impregnated with nanoparticulate silver.
10. The sterilization and humidification apparatus as claimed in claim 4, 15 wherein the sterilization and fication apparatus includes a source filter for filtering the liquid before it is passes into the wicking member.
11.The sterilization and humidification apparatus as claimed in claim 10, wherein the source filter is, or forms part of, the first filter.
12. The ization and humidification apparatus as claimed in claim 11, wherein the source filter is a porous al that filters the liquid.
13.The sterilization and humidification apparatus as claimed in claim 12, 25 wherein the porous al of the source filter is a porous ceramic with a maximum pore diameter of 0.2 microns.
14. The sterilization and humidification apparatus as claimed in claim 10, wherein the source filter is adapted to ize the liquid.
15. The sterilization and humidification apparatus as claimed in claim 14, wherein the source filter is impregnated with nanoparticulate silver.
16. The sterilization and humidification apparatus as claimed in claim 14 wherein the source filter includes silvered quartz pieces. 1O
17. The sterilization and humidification apparatus as claimed in claim 1, wherein the sterilization and humidification tus includes a second filter for filtering the gas.
18. The sterilization and humidification apparatus as claimed in claim 17, 15 wherein the second filter includes two filter media disposed sequentially in the flow of the gas, with a first filter medium being: i. disposed further upstream in the flow of gas than a second filter ; and ii. being a readily eable filter medium.
19. The sterilization and humidification apparatus as d in claim 18, wherein the readily replaceable filter medium is a washable filter.
20. The sterilization and fication apparatus as claimed in claim 18, 25 wherein the readily replaceable filter medium is a polypropylene filter.
21. The sterilization and humidification apparatus as claimed in claim 18, wherein the second filter is disposed further upstream in the flow of gas than the heating chamber.
22. The sterilization and humidification apparatus as claimed in claim 1, wherein the flow of gas through the sterilization and humidification apparatus is continuous.
23. The sterilization and humidification apparatus as claimed in claim 1, 10 wherein the flow of liquid through the sterilization and humidification apparatus is continuous.
24. The sterilization and humidification apparatus as claimed in claim 1, n the first temperature is n 180—200 degrees Celsius.
25. The sterilization and humidification apparatus as claimed in claim 1, n the heating chamber includes a heater t mounted in a conducting bulk material such that heat generated as a result of the supply of power to the heater t is transferred to the bulk material.
26. The sterilization and humidification apparatus as claimed in claim 25, wherein the bulk material is configured with a plurality of fins that se the exposure of the gas to the bulk material. 25
27. The sterilization and humidification apparatus as d in claim 1, wherein the gas is air.
28. The sterilization and humidification apparatus as claimed in claim 1, wherein the liquid is water.
29. The sterilization and humidification apparatus as claimed in claim 1, including a flow device ured to cause the gas to flow through the sterilization and humidification tus.
30. The sterilization and humidification apparatus as claimed in claim 29, wherein the flow device is a fan or pump.
31. The sterilization and humidification apparatus as claimed in claim 29, wherein the sterilization and humidification tus includes a controller for controlling the flow device. 15
32. The sterilization and humidification apparatus as claimed in claim 31, wherein the flow device is a fan and the controller ls the fan speed.
33. The ization and humidification apparatus as d in claim 1, wherein the sterilization and humidification apparatus includes a 20 controller for controlling the temperature of the heating chamber.
34. The sterilization and humidification apparatus as claimed in claim 25, wherein the sterilization and humidification apparatus includes a controller for controlling the temperature of the heating chamber.
35. The sterilization and humidification apparatus as d in 34, wherein the controller controls the power to the heater element.
36. The sterilization and humidification apparatus as claimed in claim 1, wherein the apparatus includes a bypass chamber, which provides a path for the sterilized gas to bypass the humidification chamber.
37. The sterilization and humidification apparatus as claimed in claim 36, wherein the apparatus includes a distribution adjustment mechanism that is adapted to adjust the proportion of the ized gas that passes through the humidification chamber and the proportion of the sterilized 10 gas that passes h the bypass chamber.
38. The sterilization and humidification apparatus as claimed in claim 37, wherein the distribution adjustment mechanism includes an inlet valve configured to obstruct fully and/or partially an inlet to the humidification 15 chamber and/or an inlet to the bypass chamber.
39. The sterilization and humidification apparatus as claimed in claim 37 or 38, wherein the distribution adjustment mechanism includes an outlet valve configured to obstruct fully and/or partially an outlet to the 20 fication chamber and/or an outlet to the bypass chamber.
40. The sterilization and humidification apparatus as d in claim 38, wherein the distribution adjustment mechanism includes an outlet valve configured to ct fully and or partially an outlet to the 25 fication chamber and or an outlet to the bypass chamber, and wherein the inlet valve and outlet valve e in unison.
41. The sterilization and humidification apparatus as claimed in any one of the preceding claims, wherein the sterilization and humidification apparatus es one or more sensors for sensing one or more of: i. a ature of gas in the g chamber; ii. a temperature of a heater element; iii. a humidity of the humidified gas; and iv. a temperature of the humidified gas.
42. The ization and fication apparatus as d in claim 41, 10 wherein the controller receives inputs from the sensors, and controls the flow device and/or the heating r to regulate the temperature and humidity of the humidified gas.
43. The sterilization and humidification g apparatus as claimed in claim 41, when dependent on claim 37, wherein the controller receives 15 inputs from the sensors, and controls the distribution adjustment mechanism to regulate the temperature and humidity of the humidified gas.
44. The sterilization and humidification apparatus as claimed in claim 1, 20 wherein the humidified gas is between 25—38 degrees Celsius.
45. The sterilization and humidification apparatus as claimed in claim 1, wherein the humidified gas is between 30—85% relative humidity. 25
46. An incubator including: i. a sterilization and humidification apparatus as claimed in any preceding claim; and ii. an occupancy chamber; wherein the incubator is adapted to cause the humidified gas to flow into the occupancy chamber.
47. The incubator as claimed in claim 46, including or configured for connection to one or more monitoring devices.
48. The incubator as d in claim 47, n the monitoring devices are either wired or wireless.
49. The incubator as claimed in claim 47 wherein the monitoring devices include one or more of: i. an occupancy chamber temperature sensor; ii. an occupant temperature ; and 15 iii. a pulse sensor.
50. The incubator as d in any one of claims 47 to 49, wherein the ller is configured to control the sterilization and humidification apparatus in accordance with gs from the monitoring devices.
51.The incubator as claimed in claim 46, including one or more communication ports configured for connection to one or more external devices. 25
52. The incubator as claimed in claim 46, wherein the occupancy chamber includes an inlet flow opening, for allowing the flow of the humidified gas from the ization and humidification apparatus into the occupancy chamber.
53. The incubator as claimed in claim 52, wherein the occupancy chamber includes an outlet flow g, for allowing the fluid inside the ncy chamber to flow outside the occupancy chamber.
54. The incubator as claimed in claims 53, wherein the occupancy chamber es a curved internal surface that is configured to promote the flow 10 of fluid from the inlet flow opening to the outlet flow opening.
55. The incubator as claimed in claim 46, wherein the incubator is configured to be occupied by a human baby. 15
56. The incubator as claimed in claim 55 wherein the human baby is a neonatal and/or ure baby.
57. The incubator as claimed in claim 46, wherein the incubator is predominantly made from one or more of: polyethylene; Perspex; 20 polycarbonate; fibreglass; glass; reinforced c; carbon fibre; aluminium; and stainless steel.
58. The incubator as claimed in claim 46 including an external display configured to display information concerning the operation of the 25 incubator or the status of an occupant of the incubator.
59. An incubator including: i. an occupancy chamber; ii. a first inlet for receiving an input gas; iii. a second inlet for receiving an input liquid; iv. a porous ceramic filter for ing the input liquid; and v. a heating chamber for heating the input gas so as to sterilize the input gas, wherein the incubator is configured to evaporate the input liquid into the input gas after the input liquid has passed through the porous ceramic filter, thereby producing a humidified gas at a desired temperature, which 10 is made to flow into the ncy chamber.
60. The incubator as claimed in claim 59, wherein the porous c filter includes an evaporative surface, from which the input liquid evaporates into the input gas.
Publications (1)
Publication Number | Publication Date |
---|---|
NZ607789B2 true NZ607789B2 (en) | 2015-01-06 |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2013228116B2 (en) | Sterilization and humidification apparatus and incubator | |
US11278446B2 (en) | Active thermo-regulated neonatal transportable incubator | |
EP2486334B1 (en) | Methods and devices for displacing body convection and providing a controlled personal breathing zone | |
JP2020114409A (en) | Humidification system | |
DK2694881T3 (en) | Device for temperature-controlled laminar flow | |
JP2012507321A (en) | Operating room ventilation device and method | |
WO2011031167A1 (en) | Heating and sterilisation apparatus, incubators and incubator systems | |
US20200155344A1 (en) | Cooling bed system | |
JPH04221558A (en) | Humidifier for incubator | |
CN105180296A (en) | System and method for reducing airborne contamination | |
SE532219C2 (en) | Method and apparatus for providing a clean air zone at an operating area in the medical field and use of said device | |
US7854229B2 (en) | Cradle or bed with isolation from room contamination, with controlled temperature and moisture | |
JP2004290676A (en) | Multiple plate fluid warming unit | |
DE202013105211U1 (en) | Thermoregulatory MRI device for imaging a newborn | |
NZ607789B2 (en) | Sterilization and humidification apparatus and incubator | |
NZ607789A (en) | Sterilization and humidification apparatus and incubator | |
JPH10511578A (en) | Heatable respiratory treatment humidifier | |
WO2010100559A1 (en) | Surgical instrument table ventilation devices and methods | |
CN215901131U (en) | Gas filtering device | |
Gurbeta et al. | Inspection and Testing of Pediatric and Neonate Incubators | |
DE202014103158U1 (en) | A thermoregulated neonatal transport incubator | |
EP3223767B1 (en) | Moisture control system and method | |
CA3089030A1 (en) | Air purifying vent system | |
Ahmed et al. | Low cost transportable infant incubator | |
BRMU8401251Y1 (en) | CRADLE OR BED WITH INSULATION FROM ENVIRONMENTAL CONTAMINATION, AND CONTROLLED TEMPERATURE AND HUMIDITY |