NZ724060B2 - Device management system - Google Patents
Device management system Download PDFInfo
- Publication number
- NZ724060B2 NZ724060B2 NZ724060A NZ72406015A NZ724060B2 NZ 724060 B2 NZ724060 B2 NZ 724060B2 NZ 724060 A NZ724060 A NZ 724060A NZ 72406015 A NZ72406015 A NZ 72406015A NZ 724060 B2 NZ724060 B2 NZ 724060B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- tag
- cleaning
- operator
- cleaned
- scope
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
- A61B1/12—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
- A61B1/121—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements provided with means for cleaning post-use
- A61B1/123—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements provided with means for cleaning post-use using washing machines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B90/00—Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups A61B1/00 - A61B50/00, e.g. for luxation treatment or for protecting wound edges
- A61B90/70—Cleaning devices specially adapted for surgical instruments
- A61B2090/701—Cleaning devices specially adapted for surgical instruments for flexible tubular instruments, e.g. endoscopes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/10—Apparatus features
- A61L2202/14—Means for controlling sterilisation processes, data processing, presentation and storage means, e.g. sensors, controllers, programs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/10—Apparatus features
- A61L2202/17—Combination with washing or cleaning means
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/20—Targets to be treated
- A61L2202/24—Medical instruments, e.g. endoscopes, catheters, sharps
-
- G—PHYSICS
- G06—COMPUTING OR CALCULATING; COUNTING
- G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
- G06Q10/00—Administration; Management
-
- G—PHYSICS
- G06—COMPUTING OR CALCULATING; COUNTING
- G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
- G06Q10/00—Administration; Management
- G06Q10/10—Office automation; Time management
- G06Q10/109—Time management, e.g. calendars, reminders, meetings or time accounting
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/20—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/40—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
Abstract
The present invention is directed to a device management system for monitoring the cleaning of a medical device. The claimed system includes a tag associated with the device, a cleaning module adapted to receive a validity indication that the device has been cleaned, a status device adapted to determine at least one location of the device via its proximity to the tag, and at least one process module to register an associated condition of the device depending on an operator input, wherein the operator input includes swiping the tag proximate to the at least one process module, the swiping is a short duration of swiping or a long duration of swiping, and a long duration of swiping indicates that the device requires to be cleaned within a predetermined time. The system of the present invention can track the location and determine the condition of the medical device. Based on the location and the condition, the system can also determine the storage time and the re-cleaning time of the device. rmine at least one location of the device via its proximity to the tag, and at least one process module to register an associated condition of the device depending on an operator input, wherein the operator input includes swiping the tag proximate to the at least one process module, the swiping is a short duration of swiping or a long duration of swiping, and a long duration of swiping indicates that the device requires to be cleaned within a predetermined time. The system of the present invention can track the location and determine the condition of the medical device. Based on the location and the condition, the system can also determine the storage time and the re-cleaning time of the device.
Description
DEVICE MANAGEMENT SYSTEM
FIELD OF THE INVENTION
The invention relates to a device ment system. In
particular, the invention relates, but is not limited, to a device management
system for determining a re-cleaning time of a flexible scope, such as an
endoscope, and validating the cleaning and storage times of the scope.
BACKGROUND TO THE INVENTION
Reference to background art herein is not to be construed as an
admission that such art constitutes common l knowledge in Australia
or ere.
Medical s are associated with a definitive risk of bacterial
and fungal infections. To reduce the nces of infection, guidelines
have been developed. For example, in most countries throughout the
world, flexible scopes, such as endoscopes, must be cleaned after a period
of storage. Typically, if a scope has been washed with alcohol, it can be
stored for up to 72 hours in a suitable clean storage cabinet. If no alcohol
was used, it may only be stored up to 10 hours.
Currently, to track how long a scope has been in storage, a timer
is typically set on the front of the clean e cabinet. Whilst this gives a
general idea on the amount of time the flexible scope has been in the
storage t, there are a number of shortfalls in this system. For
example, a user may incorrectly assume that the scope has been washed
in alcohol and set the storage time as 72 hours.
Furthermore, nothing in these current s tracks the amount
of time the flexible scope is out of the clean storage cabinet. Leaving
flexible scopes out of the clean storage cabinet accelerates bacterial and
fungal growth. Therefore, these scopes should be stored for a shorter
period of time before they are re-washed. rly, changes in the storage
cabinet environment may reduce the time the scopes should be stored.
However, current systems are not adapted to track and indicate how long a
flexible scope should be stored in a particular environment and whether the
scope should be re-washed.
OBJECT OF THE INVENTION
It is an aim of this invention to provide a device management
system which overcomes or ameliorates one or more of the disadvantages
or problems described above, or which at least provides a useful
alternative.
Other red objects of the t ion will become
apparent from the following description.
SUMMARY OF ION
In one form, although not necessarily the only or broadest form,
the invention resides in a device management system, the system
including:
a tag associated with a ;
a cleaning module adapted to receive a validity indication that the
device has been cleaned;
a status device adapted to determine at least one location of the
device via its proximity to the tag; and
wherein a re-cleaning time of the device is determined according to
the at least one location of the device and the validity indication that the
device has been cleaned.
Preferably, the tag is a radio frequency identification (RFID) tag.
Typically, the RFID tag is active and es its own power source.
atively, the RFID tag is passive and requires a power signal to
e. Preferably, the device is in the form of medical equipment.
Preferably, the device is a scope. ably, the device is flexible scope or
a rigid scope. Preferably, the device is an endoscope, gastroscope,
bronchoscope, duodenoscope, enterscope, ultrasound scope, toe probe,
truss probe, Brachy probe and/or ENT le or rigid scope. Typically, the
scope is in the form of an endoscope.
Preferably, the device management system includes at least one
process module. Preferably, the at least one process module is configured
to monitor workflow associated with the device. Preferably, the at least one
process module allows an operator to register whether at least one process
has been performed. Preferably, the at least one process is performed prior
to the cleaning module receiving the validity indication. Preferably, the at
least one process includes r the device has been washed, d,
leak tested, rinsed and/or manually inspected.
Preferably, the at least one s module is configured to
register an associated condition of the device depending on an operator
input. ably, the operator input is associated with the tag. For
example, the tag may be located proximate to the at least one process
module for a first predetermined time to indicate a first condition. A time
r than the first predetermined time may indicate a second condition.
Preferably, the associated condition of the device provides a related
procedure of the device. ably, the related procedure includes
cleaning the device within a predetermined time.
Preferably, the device management system includes a plurality
of process modules. Preferably, the plurality of process modules assist in
making an operator follow a sequence of processes. ably, in
response to the operator missing a process in the sequence of processes,
an indication is given to the operator by at least one of the plurality of
process modules to return to a previous process.
Preferably, the device management system includes a system
monitor. Typically, the system monitor is in communication with the
cleaning module, the status device, the tag and/or the at least one process
module. Normally, the system monitor receives information from the
cleaning , status device, the tag and/or the at least one process
module allowing the system r to monitor the current status of the
. rmore, the system monitor is adapted to provide a single
activity log from activities recorded by the at least one process module, the
cleaning module and/or the status device.
Preferably, the ng module is adapted to record information
on the tag ing when the device was cleaned and/or the cleaning
performed on the device. Even more preferably, the cleaning module
s an initial time on the tag when the device should be re-cleaned.
Alternatively, or additionally, the cleaning module may communicate with
the status device and/or the system monitor regarding when the device was
cleaned, the cleaning performed on the device and/or when the device
should be re-cleaned. Ideally, the cleaning module keeps a log of the
activities performed at the cleaning module. Preferably, the device is
cleaned by an associated cleaning unit. Preferably, the cleaning module is
configured to e the validity indication that the device has been
cleaned from the associated cleaning unit.
Normally, the ng module includes a display. The display of
the cleaning module usually indicates a current status of cleaning or the
required information needed to perform cleaning.
Typically, an operator has to be identified as being on an
authorised list by the cleaning module to undertake cleaning. Typically,
authorised cleaning operators are identified by an operator tag. Preferably,
the operator tag is an active RFID tag.
Normally, the authorised list of cleaning operators is stored on
the cleaning module. Alternatively, the authorised list of cleaning operators
is stored on the system monitor. Authorised cleaning operators are usually
added to the list of authorised cleaning operators by reading their operator
tag after authorising their operator tag to be added to the authorised list. To
authorise a cleaning or to be added to the list, lly a separate
operator tag with authorisation is read by the cleaning module.
Preferably, the status device is adapted to communicate with the
tag. ably, the cleaning module is configured to read information from
the tag regarding the sequence of ses respectively performed at the
process modules. Preferably, the cleaning module keeps a log of
information received from the tag. Typically, the status device is in the at
least one location in the form of a clean storage environment. Preferably,
the clean storage environment is a clean storage cabinet.
Normally, the status device establishes communication with the
tag when the tag is proximate and the device is in the clean storage
nment. Typically, the status device reads ation from the tag
regarding the validity indication that the device has been cleaned. In
particular, the status device usually reads information regarding when the
device was cleaned and the ng performed on the device.
Alternatively, or additionally, the status device reads information regarding
the initial time when the device should be re-cleaned.
Preferably, the status device ines the re-cleaning time of
the device according to the at least one on of the device and the
validity tion that the device has been cleaned. For example, the
status device establishes from when the device was cleaned and its time
out of the clean storage environment when the device should be re-
cleaned.
Alternatively, the status device may receive communication from
the system monitor which determines the re-cleaning time of the device
according to the at least one location of the device and the validity
indication that the device has been d. Normally, the status device
indicates when the device should be re-cleaned via a display. Preferably,
the status device is configured to determine cross-contamination.
Preferably, the status device is ured to determine cross-
contamination by determining whether the device has been processed
tly through the at least one process module and/or the validity
indication that the device has been cleaned was received.
Typically, when the device is removed from the clean storage
environment, the status device records when the device should be re-
cleaned on the tag. This information may also be communicated to the
system monitor. Preferably, the status device maintains log data on
ation received and transferred to the tag associated with the device.
Normally, the display of the status device is located on a rotary storage disc
in the clean storage cabinet.
ably, the device management system includes a storage
controller. Typically, the storage ller monitors the conditions of the
clean storage environment. That is, the storage ller monitors the
conditions of the clean storage environment in the form of the clean storage
cabinet. Ideally, depending on the ions in the clean storage
environment, the e controller sends information to adjust the time
until the device should be re-cleaned. For example, the e controller
may send information to reduce the time until the device should be re-
cleaned if the temperature in the clean storage environment is too high.
Typically, the storage controller is in communication with the
status device. Alternatively, the storage controller is in communication with
the system monitor and/or the tag. The storage controller may control
devices in the clean storage environment to maintain the clean storage
environment within predefined parameters.
Typically, the device management system includes a master
station. The master station is adapted to program the tag and or tag.
Preferably, the master station is a stand alone unit. Alternatively, the
master station is adapted to communicate with other components such as
the system monitor. The master station may lock the ation
programmed onto the tag and operator tag if required. The master station
may also keep log data of the programming of the tag and operator tag.
This log data may be communicated to the system monitor.
Normally, the device management system also includes a
receipt printer. The receipt printer is adapted to receive and print
information from any one of the tag, operator tag, cleaning module, status
device, storage controller and system r. Typically, when ic
events are recorded at the cleaning module or at the status display, a
message is sent to the receipt r for printing. For example, the receipt
printer will print when the device was cleaned, when the device was stored
into the clean storage nment, when the device was removed from
clean storage environment and when the scope should be re-cleaned.
Alternatively, or additionally, the receipt printer may read information from
the tag and print information relating to the activities of the device.
In another form, the invention resides in a method of determining
a cleaning cycle of a device, the method including the steps of:
receiving an indication that the device has been cleaned;
determining at least one location of the device via a tag associated
with the device, subsequent to receiving the indication that the
device has been cleaned; and
ining a aning time of the device ing to the at least
one location and the indication that the device has been cleaned.
Preferably, before receiving an indication that the device has
been cleaned, the method further includes loading the device in a cleaning
unit. Preferably, the step of receiving the tion that the device has
been cleaned includes receiving an indication from a cleaning unit though a
cleaning module.
ably, before receiving an indication that the device has
been d, the method further includes the step of registering whether
at least one process has been performed with the device. Preferably, the
step of registering whether the at least one process has been performed
with the device includes registering the tag with a s module.
Preferably, the step of registering whether the at least one process has
been performed with the device es registering an operator tag with
the process module to determine who performed the at least one process.
Preferably, the at least one process includes g, wiping, brushing,
leak testing, rinsing and/or manually inspecting the device.
Preferably, the step of registering whether at least one process
has been performed with the device includes registering an associated
condition of the device. Preferably, the step of registering the associated
condition of the device includes presenting the tag associated with the
device to the process module for a predetermined time. Preferably, the
ated condition of the device provides a related procedure of the
device. ably, the related procedure includes cleaning the device
within a predetermined time.
Preferably, the step of receiving an indication that the device has
been cleaned includes recording when the device was cleaned. Even more
preferably, the step of receiving an indication that the device has been
cleaned includes recording the type of cleaning for the device. ly,
the step of receiving an tion that the device has been cleaned also
includes identifying and ing the operator who cleaned the device.
Normally, before receiving an indication that the device has been
d, the method further includes the step of adding an operator to an
authorised list. Typically, the step of adding an operator to the authorised
list includes identifying an ised operator followed by identifying an
operator tag.
Preferably, the step of determining the at least one on of
the device via the tag includes ining whether the device is in a clean
storage environment. Typically, the step of determining the at least one
location of the device via the tag includes bringing the tag into proximity
with a status device. Preferably, when the tag is brought into proximity with
the status , the device is in the clean storage environment.
Preferably, the step of determining the re-cleaning time of the
device includes adjusting the re-cleaning time of the device ing on
whether the device is in or out of the clean storage environment. Normally,
the step of determining the aning time of the device also includes
adjusting the re-cleaning time of the device depending on the type of
cleaning performed on the device.
Usually, the method of determining the cleaning cycle of the
device includes monitoring parameters in the clean storage environment.
Preferably, determining the re-cleaning time of the device may be adjusted
according to the monitored parameters in the clean storage environment.
Preferably, the method of determining the cleaning cycle of the device
includes determining whether the device has been cross-contaminated
from one or more other s. Preferably, the step of ining
whether the device has been cross-contaminated includes determining
whether the other device is not clean.
Preferably, the method of determining the cleaning cycle of the
device also includes printing a receipt. Preferably, the receipt contains
information such as when the scope should be re-cleaned.
r features and advantages of the present invention will
become apparent from the following detailed description.
BRIEF DESCRIPTION OF THE DRAWINGS
By way of example only, preferred embodiments of the ion
will be described more fully after with reference to the accompanying
figures, wherein:
Figure 1 illustrates a schematic of a device management system
according to an embodiment of the ion;
Figure 2 illustrates a flow diagram for determining a cleaning cycle of
the device; and
Figure 3 illustrates a flow diagram illustrating part of a process path
in Figure 2.
DETAILED DESCRIPTION OF THE GS
Figure 1 illustrates a device management system 1 ing to
an embodiment of the invention. The device management system 1
includes a device in the form of a scope 10, a tag 20, an operator tag 30, a
master station 100, process modules 220, a cleaning module 240, a status
device 300, a e controller 400, a system monitor 500, a receipt
printer 600 and a network 700.
The tag 20 is ed to the scope 10. The tag 20 and operator
tag 30 are adapted to store and process information along with transferring
and receiving information. In this embodiment, the tag 20 and operator tag
are in the form of radio frequency identification (RFID) tags. The tag 20
and operator tag 30 are active RFID tags and include their own battery
power. However, it would be appreciated by a person skilled in the art that
the tag 20 and operator tag 30 may be passive and require a power signal
from the reader device to operate.
In this embodiment, the master station 100 operates as a stand-
alone . However, the master station 100 includes a communication
ace to communicate with other components such as the process
modules 220, the cleaning module 240, status device 300, storage
ller 400, system monitor 500 and receipt printer 600, in the device
management system 1, via the network 700. The communication interface
of the master station 100 may also icate with other components
external to the device management system 1.
The master station 100 programs the tag 20 and operator tag
. In particular, the master n 100 programs the tag 20 with
information including i) a Unique Identification Number (UID); ii) the type of
scope 10; iii) the name of the scope 10; iv) the amount of time the scope 10
is allowed outside of a clean storage environment once it has been
cleaned; and v) the length of time the scope 10 can be stored in the clean
storage environment. Moreover, the master station 100 may program a
particular process or clean path for the scope 10. For example, the scope
may be required to proceed through the process modules 220 and
cleaning module 240, as outlined below, or may proceed directly to the
cleaning module 240.
Further to the above, data entered into the master station 100
and/or onto the tag 20, may also allow the identity of the scope 10 to be
established. For example, if a particular e of the scope 10 is entered
as data, along with the associated brand name of the scope 10, the type of
scope 10 may be established.
The master station 100 also programs the operator tag 30 to
include information such as the name of the operator and whether they are
a washer operator or a washer iser, as further discussed below. The
master station 100 may also be used to program other l tags as
required by the device management system 1.
Once the tag 20 and operator tag 30 have been programmed,
they can be used with the other ents in the device management
system 1. If required, the master station 100 may lock the information on
the tag 20 and operator tag 30 so that this information cannot be altered.
Furthermore, the master station keeps log data on the programming of the
tag 20 and operator tag 30 for future reference and auditing.
The s modules 220 monitor operator workflow associated
with the scope to before proceeding to an automatic cleaning unit
associated with the cleaning module 240. That is, the s modules 220
allow the operator to register whether certain processes have been
performed before ding to the cleaning unit or elsewhere. As outlined
below, five separate processes are aken in this embodiment before
proceeding to the ng unit. However, as would be appreciated by a
person skilled in the art, further processes may be added as required or
dictated by guidelines or regulations.
The process s 220 in this embodiment are configured to
register associated conditions of the scope 10 depending on an operator
input. That is, the operator may register a short swipe or a long swipe with
the process s 220. The short swipe may, for instance, involve
holding the tag 20 proximate to the s module 220 for less than 4
second. The long swipe may, for instance, involve holding the tag 20
proximate to the process module 220 for greater than 4 second. The long
swipe may indicate that the scope to is heavily soiled and requires to be
cleaned within a predetermined time.
Further to the above, five process modules 220 in the form of
process modules 220a, 220b, 220c, 220d, 220e are located at five work
stations in this embodiment. The first process module 220a is associated
with an operating theatre. The first s module 220a allows the
operator to register that the scope to has been washed/wiped with
detergent after being used on a patient. The process module 220a is
configured to record on the tag 20 that the scope to has been
/wiped after the operator swipes their operator tag 30 proximate to
the first s module 220a followed by the tag 20. This process also
allows the identity of the operator to be recorded on the tag 20.
Furthermore, depending on the on of the swipe of the tag
(Le. a short swipe or long swipe), an associated condition of the scope
to is registered on the tag 20. For e, if a long swipe is registered
(i.e. greater than four s), the scope is identified as being heavily
soiled and requires cleaning to be completed within one hour.
The second process module 220b is associated with a first sink
station. The second s module 220b allows the operator to register
that channels (i.e. tubes) within the scope to have been brushed
dually (according to guidelines). To this end, it is noted that if the
washing/wiping of the scope to has not been registered on the tag 20 by
the process module 220a, when registering that the channels within the
scope to have been brushed individually, a display on the process module
220b will direct the operator back to wash/swipe the scope to at the
previous stage.
Accordingly, the process modules 220 assist in preventing
ors missing processes in cleaning/maintaining the scope 10.
Furthermore, as would be appreciated, the process modules 220 may
assist in making operators follow a particular sequence of processes with
the scope 10.
The process module 220b is configured to record on the tag 20
that the channels of the scope to have been brushed individually after the
operator swipes their operator tag 30 proximate to the second process
module 220b followed by the tag 20. This process also allows the identity of
the operator to be recorded on the tag 20.
Furthermore, similar to the above, the operator may register an
associated condition of the scope 10 depending on an operator input. For
example, the operator may swipe (i.e. leave the tag 20 proximate to the
process module 220b) for more than four seconds to indicate that the
scope 10 requires an alternative treatment than that provided at s
module 220c below.
The third process module 220c is associated a second sink
station. The third process module 220c allows the operator to register that
the scope 10 has been manually washed and rinsed (according to
guidelines). Similar to the above, it is noted that if the washing/wiping of the
scope 10 and/or brushing of the channels in the scope 10 has not been
registered on the tag 20, a display on the process module 220c will direct
the operator back to the previous stage(s).
The process module 220c is configured to record on the tag 20
that the scope 10 has been manually washed and rinsed after the operator
swipes their operator tag 30 proximate to the third process module 220c
followed by the tag 20. This process also allows the identity of the operator
to be recorded on the tag 20.
Furthermore, similar to the above, the operator may register an
associated ion of the scope 10 depending on an operator input. For
example, the operator may swipe (i.e. leave the tag 20 ate to the
s module 220c) for more than four seconds to indicate that the
scope 10 requires an alternative treatment than that provided at process
module 220d below.
The fourth process module 220d is ated with a leak testing
apparatus. The third s module 220d allows the operator to register
that the scope 10 has been leak tested (according to guidelines). r to
the above, if one of the stages at s modules 220a, 220b, 220c has
been missed, the fourth process module 220d will redirect the operator to
the required s or the required sequence of processes.
The s module 220d is configured to record on the tag 20
that the scope to has been leak tested after the operator swipes their
operator tag 30 proximate to the fourth process module 220d followed by
the tag 20. This s also allows the identity of the operator to be
recorded on the tag 20.
Furthermore, similar to the above, the operator may register an
associated condition of the scope 10 depending on an operator input. For
example, the operator may swipe (i.e. leave the tag 20 proximate to the
process module 220d) for more than four seconds to indicate that the
scope 10 requires an alternative ent. That is, for instance, if the
scope to fails the leak test its seals may have to be replaced.
The fifth process module 220e is associated with a manual
inspection. The fifth process module 220e allows the operator to register
that the scope to has been manually inspected (according to ines).
Similar to the above, if one of the stages at process modules 220a, 220b,
220c, 220d has been , the fifth s module 220e will redirect the
or to the required process or the required sequence of processes.
The process module 220e is configured to record on the tag 20
that the scope to has been manually inspected after the operator swipes
their operator tag 30 proximate to the fifth process module 220e followed
by the tag 20. This process also allows the identity of the operator to be
recorded on the tag 20.
Furthermore, similar to the above, the operator may register an
ated condition of the scope 10 depending on an operator input. For
example, the operator may swipe (i.e. leave the tag 20 proximate to the
process module 220e) for more than four seconds to indicate that the
scope 10 requires an alternative treatment.
The cleaning module 240 s the cleaning of the scope 10 in
an associated cleaning unit. For example, the cleaning module 240 records
whether a short, standard or long wash has been used to clean the scope
in the associated cleaning unit. Furthermore, other parameters such as
whether alcohol was used in the clean cycle are recorded. In this regard,
the cleaning module 240 is ured to receive a validity indication from
the ated cleaning unit that the scope 10 has been cleaned according
to a particular wash cycle.
The cleaning module 240 is d to receive and transfer
information to the tag 20 and operator tag 30. In this regard, the cleaning
module 240 is similar to the process modules 220. The cleaning module
240 keeps a log file of the data received and transferred to and from the tag
and operator tag 30. This log file may include the tag 20 UID, the
number of cleaning cycles the scope 10 has been through, the sequence of
processes med at the process modules 220, the name of the
operator who cleaned the scope 10, time and date. Furthermore, cleaning
module 240 has a display to view the data received and erred to and
from the tag 20 and or tag 30. The cleaning module 240 is also
adapted to communicate with other components in the device management
system 1, such as the status device 300, system monitor 500 and receipt
printer 600, via the network 700. This communication interface may also
communicate with other components external to the device management
system 1. However, as would be appreciated by a person skilled in the art,
the cleaning module 240 may be a standalone unit that communicates
primarily with, for example, the tag 20 or or tag 30.
The status device 300 is adapted to read information stored on
the tag 20 and send information to the tag 20. The status device 300 is in
communication with other components in the device management system
1, such as the process modules 220, the cleaning module 240, storage
controller 400, system r 500 and receipt printer 600, via the network
700. Again however, as would be iated by a person skilled in the art,
the status device 300 may be a standalone unit that communicates
ily with, for example, the tag 20 or or tag 30.
The status device 300 determines the amount of time remaining
until the scope to must be re-cleaned. The status device 300 displays the
amount of time remaining until the scope to must be re-cleaned via a LED
display. The status device 300 maintains log data on information received
from the tag 20 and the other components in the device management
system 1. The status device 300 is located on a rotary disc in the clean
storage environment in the form of a clean storage cabinet (not shown)
where the scope to is stored. The rotary disc is adapted to store a number
of scopes 10 about a central pole in the clean storage cabinet and each
scope to is associated with one status device 300.
The status device 300 is also configured to assist in determining
cross-contamination. That is, if the status device 300 detects, via the tag
, that the scope to has not been processed correctly through the
process modules 220 or a validity indication has not been received from the
cleaning unit and/or the cleaning module 240, the status device 300 is
configured to indicate that other scopes adjacent thereto have been
contaminated. For example, the LED displays may indicate that the scope
to and the scopes adjacent thereto must be aned.
The storage controller 400 monitors and controls conditions in
the clean e cabinet. The storage controller 400 is in communication
with the other components in the device management system 1, such as
the status device 300 and system monitor 500, via the network 700.
Furthermore, the storage controller 400 maintains a log of the conditions in
the clean e cabinet. In particular, the e controller 400 monitors
parameters such as air quality, temperature, humidity, r the door of
the t is open and the flow of clean air through the scope to in the
clean storage cabinet. The storage controller 400 is adapted to alert a user
when the clean e cabinet is not within a predefined parameter. For
e, if the air quality is determined to be e an acceptable range,
the storage controller 400 may indicate that a HPEA filter in the storage
cabinet needs replacing. Alternatively, or additionally, the storage controller
400 may control devices in the clean storage cabinet to maintain the
t within predefined parameters.
The storage monitor 400 is also adapted to control a lock to a
door that is part of the clean storage cabinet. To activate and open the lock,
the operator tag 30 needs to be registered at storage controller 400. This
allows a record of who accessed the cabinet to be recorded. Furthermore,
the lock can be programmed to interlock the ) to a room on a ‘pass
through’ version of the cabinet. This stops the cabinet door being open at
the same time as the doors to the room and, therefore, prevents direct
airflow from one room to another via the clean e cabinet.
The system monitor 500 is used to provide a single view point of
the components in the device management system 1. In this regard, the
system monitor 500 is able to monitor and collate the log data from the
other ents in the device management system 1. In particular, the
system monitor 500 can query the current status of the scope 10, typically
via the status device 300, and provide a summary of the recent activity at
the process modules 220 and cleaning module 240. It will be appreciated
by a person skilled in the art that the system r 500 may determine
the re-cleaning time of the scope 10 from ation received from the
other components in the device management system 1.
The receipt printer 600 is adapted to receive and print
information from the master station 100, process modules 220, cleaning
module 240, status device 300, storage controller 400 and system monitor
500 via the network 700. However, the receipt printer 600 may also ly
receive and print information from the tag 20 and operator tag 30 through a
reader on the receipt printer 600.
The network 700 in this ment is a RS485 network.
However, it would be appreciated by a person skilled in the art that network
700 may take a variety of other forms ing wireless. The network 700
may include a data box to monitor and/or manage data on the network 700.
The data box may include a display that allows an operator to view how
many devices (i.e. scopes 10) are on the network 700. Furthermore, the
data box may be configured to manage data on the k 700 in order to
reduce the amount of traffic on the network 700. For example, if a tag 20 is
in ittent ication with the status device 300, due to its location,
a number of data parcels will be created indicating whether the scope 10 is
in or out of the clean storage environment. The data box may moderate
these data parcels (i.e. provide a lower sampling rate) to reduce the
amount of traffic on the k 700. Moreover, the data box may buffer
the data on the network 700 if, for instance, the system r 500 has
been switched off.
Figure 2 illustrates a flow diagram of determining a cleaning
cycle of the scope 10 (Le. when the scope 10 should be re-cleaned)
according to an aspect of the invention with reference to figure 1.
At step 1000, before processing or cleaning the scope 10, an
operator must be registered to perform such operations. To do this, an
authoriser must swipe their operator tag 30 such that the master station
100 reads the operator tag 30. Following this, the operator presents their
own operator tag 30 to the master station 100, which will then add the
or to an authorised list. It would be appreciated that the authoriser
may also directly add the operator to the authorised list with the master
station 100 by programming the operator’s tag 30, in which case, the
authoriser may not be required to swipe their or tag 30.
Once the operator is added to the authorised list, they can
perform the processes associated with process modules 220 and operate
2015/050042
the cleaning unit associated with the cleaning module 240 (depending on
their authorisation level).
At step 2000, the operator performs a sequence of processes on
the scope 10. The processes performed on the scope to are outlined
further in figure 3.
At step 2100, the operator proceeds to manually wash/wipe the
scope to down after being used on a patient. After washing/wiping down
the scope 10, the operator places their operator tag 30 proximate to the
first process module 220a. Following this, the operator places the tag 20
proximate to the first process module 220a. This registers on the tag 20
that the operator has initially washed/wiped down the scope to after being
used on a patient. The identity of the operator who washed/wiped down the
scope to is also registered on the tag 20.
Furthermore, depending on how long the operator holds the tag
ate to the first process module 220a, an associated condition of
the scope to is registered on the tag 20. In the embodiment, the operator
holds the tag 20 proximate to the first process module 220a for less than a
predetermined time (i.e. 4 seconds) ting that the scope to is not
heavily soiled. If, however, the operator held the tag 20 proximate to the
first process module 220a for greater than the ermined time, this
would te that the scope to is heavily soiled and needs to be
processed with a predefined time (i.e. one hour).
At step 2200, the operator proceeds to the first sink to brush the
inner ls of the scope 10. After brushing the channels of the scope
, the operator places their or tag 30 proximate to the second
process module 220b. Following this, the operator places the tag 20
ate to the second process module 220b. This registers on the tag 20
that the operator has brushed the channels of the scope 10. The identity of
the operator who brushed the channels of the scope 10 is also registered
on the tag 20.
Further to the above, it would also be appreciated that the
operator may register an associated ion of the scope 10 at step 2200.
In addition, it will also be appreciated that if the operator missed step 2100,
they will be directed back to step 2100 at step 2200 by the second process
module 220b.
At step 2300, the operator proceeds to the second sink to
manually wash and rinse the scope 10. After manually washing and rinsing
the scope 10, the operator places their operator tag 30 proximate to the
third process module 220c. Following this, the or places the tag 20
proximate to the third process module 220c. This ers on the tag 20
that the operator has manually washed and rinsed the scope 10. The
identity of the operator who ly washed and rinsed the scope 10 is
also registered on the tag 20.
Further to the above, it would also be iated that the
operator may register an associated condition of the scope 10 at step 2300.
In addition, it will also be appreciated that if the operator missed steps 2100
and/or 2200, they will be directed back to either step 2100 and/or 2200 at
step 2300 by the third process module 220c.
At step 2400, the operator proceeds to the leak g
apparatus to perform a leak test on the scope 10. After performing the leak
test on the scope 10, the or places their operator tag 30 proximate to
the fourth process module 220d. Following this, the operator places the tag
proximate to the fourth process module 220d for a period of time less
than the predetermined time. This registers on the tag 20 that the operator
has successfully performed a leak test on the scope 10. The identity of the
operator who performed the leak test on the scope 10 is also registered on
the tag 20.
r to the above, it would also be appreciated that the
operator may register that the scope 10 failed the leak test and requires
maintenance by, for example, placing the tag 20 proximate to the fourth
process module 220d for a period of time greater than the predetermined
time. In addition, it will also be appreciated that if the operator missed steps
2100, 2200 and/or 2300, they will be directed back to either step 2100,
2200 and/or 2300 at step 2400 by the fourth process module 220d.
At step 2500, the or proceeds to perform a manual
inspection on the scope 10. After manually inspecting the scope 10, the
operator places their operator tag 30 proximate to the fifth s module
220e. Following this, the operator places the tag 20 proximate to the fifth
process module 220e for a period of time less than the predetermined time.
This registers on the tag 20 that the operator has inspected the scope 10
and it appears fit for use. The identity of the operator who performed the
manual inspection on the scope 10 is also registered on the tag 20.
Further to the above, it would also be appreciated that the
operator may register that the scope 10 is currently not fit for use by, for
example, g the tag 20 ate to the fifth process module 220e for
a period of time greater than the ermined time. In addition, it will also
be appreciated that if the operator missed steps 2100, 2200, 2300 and/or
2400, they will be directed back to either step 2100, 2200, 2300 and/or
2400 at step 2500 by the fifth process module 220e.
At step 3000, the scope 10 is cleaned by being put through a
wash cycle of the automatic cleaning unit. It would be appreciated that if
the operator has missed any one of steps 2100 to 2500, the cleaning
module 240 will direct the operator back to any one of these steps when
the tag is ted thereto.
A clean cycle is pre-programmed by the operator before the
scope 10 is cleaned in the cleaning unit. After the scope 10 is cleaned, the
operator presents their operator tag 30 to the ng module 240. The
cleaning module 240 then s who performed the clean on the scope
Following the above, the cleaning module 240 will then prompt
the washer operator to present the tag 20 of the scope 10. The cleaning
module 240 writes the time the scope to is removed as well as the washer
operator detail to the tag 20. Moreover, when the tag 20 is presented to the
cleaning module 240, an initial time until re-cleaning of the scope 10 will be
set. This initial time will be displayed in green on the display of the cleaning
module 240. Furthermore, the initial re-cleaning time of the scope to will be
recorded by the cleaning module 240 and on the tag 20. As mentioned
above, this initial time re-cleaning time will be determined by the type of
clean the scope to has been put through (i.e. short, long, l, non-
alcohol etc) and the pre-programmed scope time limit parameters.
In addition, in the current embodiment, when the tag 20 is
presented to the cleaning module 240, it is assumed that the scope to is
out of the clean storage cabinet as the tag is not in communication with the
status device 300. ingly, the time scope to is out of the clean
storage environment is recorded.
At step 4000, the tag 20 of the scope to is d proximate to
the status device 300 in the clean storage cabinet. That is, in the clean
storage cabinet, the scope to is stored such that the tag 20 and status
device 300 are within a short range and able to communicate. This short
range prevents communication interference from other scopes 10 and
status s 300 within the clean e cabinet. Furthermore, the
storage of the scope to is such that the status device 300 can determine
whether the scope to is in the clean storage cabinet. It will be appreciated
that multiple status s 300, each with a unique ID, in one or more
cabinets determines where each scope tag 20 is exactly located within the
system and, via the network 700, may be displayed on a screen. In
2015/050042
addition, with information received from the tag 20, the status device 300
determines the re-cleaning time of the scope 10 according to how long the
scope 10 was out of the clean storage environment and information ng
to the cleaning of scope 10.
A display of the status device 300 shows the time remaining until
the scope 10 should be re-cleaned. Before the tag 20 is located proximate,
the status device 300 displays that no scope is present. When the tag 20 is
proximate to the status device 300 and communication is established, the
status device 300 will display the status of the scope 10. In particular, if the
allowed time for the scope 10 being out of a clean e environment has
been exceeded, the status device will flash “00:00” in the colour red. In
some cases, the scope 10 may be erred between clean storage
environments and therefore, if the allowable storage time of the scope 10
has been exceeded, the status device 300 will also flash “00:00” in the
colour red. If the scope 10 has time remaining before the scope has to be
re-cleaned, the status device 300 will display the time remaining until the
next clean of the scope 10 in the colour green.
In certain circumstance, during the e of the scope 10, the
storage controller 400 may also communicate with the status device 300
and/or the tag 20 to adjust the remaining time until the scope 10 has to be
re-cleaned. For example, if the door of the clean storage cabinet is left
open, the storage ller 400 may send information to adjust the out of
clean storage environment time left for the scope 10. Similarly, if a high
temperature is recorded in the clean storage cabinet, the remaining e
time may be reduced. Separately, if cross-contamination is detected by, for
example, a contaminated scope entering into the clean storage
environment, the status device 300 may indicate that the scope 10 is now
contaminated, via its display, and record that the scope 10 is contaminated
on the tag 20.
If during storage, the maximum storage time of the scope to is
exceeded, the display of the status device 300 will turn red and show the
exceeded storage time of the scope 10. In this case, an operator should
remove the scope to and take it to be aned per step 8000.
On the other hand, if the scope to does not need to be re-
cleaned, at step 5000, the scope to is d from the clean storage
cabinet for use during a medical operation. It would also be appreciated
that the scope may proceed directly from the washer unit to be used in a
medical operation.
When the scope to is removed from the clean storage cabinet,
communication is lost n the tag 20 and the status device 300.
Accordingly, this indicates that the scope is out of the clean storage
environment and the time the scope to is out of a clean storage
environment continues to be recorded. On tag 20, the remaining allowable
clean e time left for the scope to is also recorded.
During step 5000, a t from the receipt printer is collected.
This receipt contains information ed from the cleaning module 240
and status device 300 during steps 1000 to 4000. In particular, this receipt
contains information regarding when the device was stored into the clean
storage nment, when the device was removed from clean storage
environment and when the scope should be re-cleaned if it is no longer
stored in the cleaning storage environment.
At step 6000, the print-out from the receipt printer 600 is
attached to the scope to and then the scope to is then taken off to be used
in a medical operation at step 7000. Before the operation occurs, the
receipt from the receipt printer 600 can be checked to ensure that scope to
is fit for use (i.e. the scope to does not have to be re-cleaned as the out of
clean storage time has not been exceeded). Furthermore, if one is unsure
whether the scope 10 should be used, it may be returned to a reader such
as the receipt printer 600 to check whether the scope 10 is still fit for use.
After the scope 10 has been used in the medical procedure, it is then
typically returned to the cleaning unit for aning.
As the scope 10 proceeds through steps 1000 to 8000, the
system monitor 500 can be used to query the current status of the scope
. It may also provide a summary of the recent or current activity at the
cleaning unit via the cleaning module 240 and the history of the clean
storage cabinet via the storage controller 400.
The device ment system 1 provides facilities to allow
tracking and auditing of both scope 10 and operator activities. In particular,
the device management system 1 tracks the time scope 10 is in and out of
a clean storage nment and when the scope should be re-cleaned.
Furthermore, the s modules 220 assist in making the operator follow
a sequence of maintenance/cleaning steps before the scope 10 is cleaned
in the cleaning unit. This substantially assists in infection control. Similarly,
the type of cleaning performed on the scope 10 is recorded, which assists
in determining when the scope should be re-cleaned. Furthermore, the
device management system 1 ensures that only trained operators are using
the device management system 1.
Other recordable parameters may also be ed including,
but not d to, environmental inputs, air pressure and vacuum flow
either within the cabinet or within each scope 10.
In addition, the device management system 1 substantially
assists in creating a maintenance schedule or cleaning schedule for the
scopes 10. That is, as the device management system 1 is adapted to track
multiple scopes 10 across a number of storage cabinets, a user can view
the status of the scope 10 in real time and schedule which scopes 10
needs to be cleaned. Similarly, the device management system 1 s in
determining when there is a problem in the clean storage cabinet via the
storage controller 400, which may require maintenance or some further
ion. rmore, the system 1 assist in preventing cross-
contamination between scopes.
The receipt printer 600 produces a duplicate copy of the e
time and shows the last time the scope can be used before re-cleaning.
This avoids having to install multiple s through out the hospital to
check the status of scope 10 before use. Accordingly, the duplicate copy
validates the scope as ‘fit for use’ at the bedside without additional devices
or displays needed in places such as hospital theatres.
The device management system 1 is also a stand alone modular
system but can interact with other networks if required. For example, the
device management system 1 may be integrated with a hospital server and
provide remote . In addition, as would be appreciated by a person
skilled in the art, as the tag 20 is able to store sufficient data, the process
modules 220, cleaning modules 240 and/or status device 300 may be
standalone units. This reduces the need for network infrastructure, as data
is carried on the tag 20, and allows the management system 1 to be
easily/cost effectively installed.
All devices in the device management system 1 can be re-
programmed or updated externally. Use of common processors allows
several devices to be re-programmed. For example, a tag reader can
become a tag writer or storage controller 400, depending upon software.
The system can also be adapted for other purposes such as, but
not limited to, instrument storage cabinets, asset ng in hospitals and
so forth.
In this specification, adjectives such as first and second, left and
right, top and bottom, and the like may be used solely to distinguish one
t or action from another element or action t necessarily
ing or implying any actual such relationship or order. Where the
context permits, nce to an integer or a component or step (or the like)
is not to be interpreted as being limited to only one of that integer,
component, or step, but rather could be one or more of that r,
component, or step etc.
] The above ption of various embodiments of the present
invention is provided for purposes of description to one of ordinary skill in
the related art. It is not intended to be exhaustive or to limit the invention to
a single disclosed embodiment. As mentioned above, numerous
alternatives and variations to the present invention will be apparent to those
d in the art of the above teaching. ingly, while some alternative
embodiments have been discussed specifically, other embodiments will be
apparent or vely easily developed by those of ordinary skill in the art.
The invention is intended to embrace all alternatives, modifications, and
variations of the present invention that have been discussed herein, and
other embodiments that fall within the spirit and scope of the above
descnbedinvenfion.
In this specification, the terms ‘comprises’, ‘comprising’,
‘includes’, ‘including’, or similar terms are intended to mean a non-exclusive
ion, such that a method, system or apparatus that comprises a list of
elements does not include those elements solely, but may well include
other elements not listed.
Claims (15)
1. A device management system, the system including: a tag associated with a device; at least one process module configured to register an associated condition of the device depending on an operator input, wherein the operator input includes g the tag proximate to the at least one process module, the swiping is a short duration of g or a long duration of swiping, and a long duration of swiping tes that the device requires to be cleaned within a predetermined time; a cleaning module adapted to receive a validity indication that the device has been cleaned; and a status device adapted to determine at least one location of the device via its proximity to the tag; n a aning time of the device is determined by the validity indication that the device has been cleaned and the at least one location of the device determined from the status device.
2. The system of claim 1, wherein the long duration of swiping the tag indicates that the device is heavily soiled and requires cleaning to be ted within one hour, wherein the long duration of swiping is r than four seconds.
3. The system of claim 1 or 2, wherein the cleaning module is adapted to record information on the tag regarding when the device was cleaned and/or the cleaning performed on the device; and/or the re-cleaning time of the device is adjusted depending on whether the device is in or out of a clean storage environment; and/or the cleaning module records an initial time on the tag when the device should be re-cleaned; and/or the status device is configured to ine cross-contamination by determining whether the ty indication that the device has been cleaned was received.
4. The system of any one of the preceding claims, wherein the status device determines the re-cleaning time of the device according to the at least one location of the device and the ty indication that the device has been cleaned.
5. The system of claim 4, wherein the status device is located in a clean storage cabinet and when the device is removed from the clean storage environment, the status device records when the device should be re-cleaned on the tag.
6. The system of any one of the preceding claims, wherein the at least one process module allows an operator to register r at least one process has been performed on the device.
7. The system of claim 6, wherein the at least one process includes one or more of the device being washed, brushed, leak tested, rinsed and/or manually ted; and/or the status device is configured to determine cross-contamination by ining whether the device has been processed correctly through the at least one process module.
8. The system of any one of the preceding claims, wherein the system includes a plurality of s modules that assist in making an operator follow a sequence of processes, and in response to the operator missing a process in the sequence of processes, an indication is given to the operator by at least one of the plurality of process modules to return to a previous process.
9. The system of any one of the ing , wherein the device management system includes a storage controller that monitors conditions of the clean storage environment, and depending on the conditions in the clean storage environment, the storage controller sends information to adjust the time until the device should be aned.
10. A method of determining a ng cycle of a device, the method including the steps of: registering an associated condition of the device depending on an operator input, wherein the operator input includes swiping a tag proximate to at least one process module, the g is a short duration of swiping or a long duration of g; cleaning the device according to the condition registered to the at least one process module, wherein the device is cleaned within a predetermined time if the operator input is a long duration of swiping; receiving an indication that the device has been cleaned; determining at least one location of the device via the tag, subsequent to receiving the indication that the device has been cleaned; and determining a re-cleaning time of the device according to the at least one location and the indication that the device has been d.
11. The method of claim 10, wherein the long duration of g the tag indicates that the device is heavily soiled and the step of cleaning the device is to be completed within one hour, wherein the long duration of swiping is greater than four seconds.
12. The method of claim 10 or 11, wherein the step of determining the re-cleaning time of the device includes adjusting the re-cleaning time of the device depending on whether the device is in or out of a clean storage environment; and/or the step of ing the indication that the device has been cleaned includes receiving an indication from a cleaning unit at a cleaning module; and/or before receiving an indication that the device has been cleaned, the method further includes the step of adding an operator to an ised list; and/or the step of determining the at least one location of the device via the tag includes determining whether the device is in a clean storage cabinet.
13. The method of any one of claims 10 to 12, wherein before receiving an indication that the device has been cleaned, the method further includes the step of ering whether at least one process has been performed with the device.
14. The method of claim 13, wherein the at least one s includes one or more of the device being washed, brushed, leak tested, rinsed and/or manually inspected; and/or the step of registering whether the at least one process has been performed with the device includes further registering an associated condition of the .
15. The method of any one of claims 10 to 14, wherein the method further includes determining whether the device has been cross-contaminated from one or more other devices; and/or printing a receipt that can be checked to ensure that the device is fit for use prior to an operation.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2014900373 | 2014-02-07 | ||
| AU2014900373A AU2014900373A0 (en) | 2014-02-07 | Device management system | |
| PCT/AU2015/050042 WO2015117203A1 (en) | 2014-02-07 | 2015-02-06 | Device management system |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ724060A NZ724060A (en) | 2020-10-30 |
| NZ724060B2 true NZ724060B2 (en) | 2021-02-02 |
Family
ID=
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