BHM Medical Ministand Instructions For Use Manual

Type
Instructions For Use Manual

BHM Medical Ministand is part of a series of quality products designed especially for hospitals, nursing homes and other health care uses. The device can be used for lifting and transferring a person, and it comes with a variety of features to ensure the safety and comfort of both the patient and the caregiver. Some of the key features of the Ministand include:

  • Adjustable width legs: The legs of the Ministand can be adjusted to accommodate different patient sizes and needs.
  • Power Base Models: The Ministand is available with a variety of power base models to meet the specific needs of your facility.

BHM Medical Ministand is part of a series of quality products designed especially for hospitals, nursing homes and other health care uses. The device can be used for lifting and transferring a person, and it comes with a variety of features to ensure the safety and comfort of both the patient and the caregiver. Some of the key features of the Ministand include:

  • Adjustable width legs: The legs of the Ministand can be adjusted to accommodate different patient sizes and needs.
  • Power Base Models: The Ministand is available with a variety of power base models to meet the specific needs of your facility.
001.20075.EN rev.6
September 2010
Ministand
Instructions for Use
Printed in Canada 2010
BHM medical products are patented or patent pending.
Our policy is one of continuous development, and we therefore reserve the right to make
technical alterations without notice. The content of this publication may not be copied either whole
or in part without our consent.
General Information
2
General Information ..................................................................................................................2
Foreword.............................................................................................................................................................3
Service and Support ...........................................................................................................................................3
Manufacturer Information....................................................................................................................................3
Authorized European Representative.................................................................................................................3
Definitions Used in this Manual ..........................................................................................................................4
Intended Use.......................................................................................................................................................4
Operational Life...................................................................................................................................................5
Equipment Identification .....................................................................................................................................5
Verifying the Package Contents .........................................................................................................................5
Policy on Number of Staff Members Required for Patient Transfer...................................................................5
Symbols Used........................................................................................................................................6
Safety Instructions and Warnings............................................................................................7
General Instructions...............................................................................................................................7
General...............................................................................................................................................................7
Electric Shock Prevention...................................................................................................................................8
Fire and Explosion Prevention............................................................................................................................8
Battery Safety Practices .....................................................................................................................................9
Equipment Warning Labels.................................................................................................................................9
Sling Compatibility..................................................................................................................10
Operating the Ministand..........................................................................................................11
Introduction...........................................................................................................................................11
Adjusting the Width of the Legs........................................................................................................................11
Power Base Models..........................................................................................................................................12
Correct Use of the Brakes ................................................................................................................................12
Brakes application and release:........................................................................................................................12
Emergency Shut-Off .........................................................................................................................................12
Battery Pack......................................................................................................................................................13
Removable Battery Pack..................................................................................................................................13
Charging the Battery.........................................................................................................................................13
Maintenance Indicator ......................................................................................................................................13
Raising and Lowering the Patient.........................................................................................................13
To raise the patient:..........................................................................................................................................13
To lower the patient: .........................................................................................................................................13
Active Sling Installation ........................................................................................................................14
Attaching the active sling to the Ministand...........................................................................................14
Transferring the Patient........................................................................................................................13
Before Lifting the Patient: .................................................................................................................................13
Main Actuator Failure........................................................................................................................................13
Disinfection, Cleaning and Maintenance...............................................................................13
Lift Cleaning and Care..........................................................................................................................13
BHM Sling Maintenance...................................................................................................................................13
Monthly Inspection ...............................................................................................................................13
Checklist Before Use............................................................................................................................13
Troubleshooting Guide...........................................................................................................13
Technical Specifications.........................................................................................................13
Limited Warranty.....................................................................................................................13
General Information
General Information
3
Thank you for purchasing the Ministand™.
Your Ministand™ is part of a series of quality
products designed especially for hospitals,
nursing homes and other health care uses.
We are dedicated to serving your needs and
providing the best products available along
with training that will bring your staff
maximum benefit from every BHM Medical
product.
Please read this manual thoroughly, and
contact us if you have any questions about the
operation or maintenance of your BHM
Medical equipment.
Foreword
Please read this manual in its entirety before
using your Ministand™. The information in
this manual is crucial to the proper operation
and maintenance of the equipment, and will
help protect your product as well as ensure
that the equipment performs to your
satisfaction. Lifting and transferring a person
always presents a potential risk. Some of the
information in this manual is important for
your safety and must be read and understood
to help prevent injuries. BHM Medical
strongly advises and warns that to avoid
injuries that can be attributed to the use of
inadequate parts, only parts designated by
BHM Medical should be used on equipment
and other appliances supplied by
BHM Medical.
Furthermore, unauthorized modifications on
any BHM Medical equipment may affect its
safety. BHM Medical will not be held
responsible for any accidents, incidents or
deficiencies of performance that occur as a
result of any unauthorized modification to its
products.
Tested according to standards by:
Product Service and
Service and Support
A service routine has to be performed on your
Ministand™ by qualified personnel to ensure
the safety and proper operation of your
product. See “Disinfection, Cleaning and
Maintenance” section.
If you require further information, please
contact your local BHM Medical
representative, who can offer comprehensive
support and service programs to maximize the
long term safety, reliability and value of the
product. You can also contact your local
BHM Medical representative for replacement
parts.
Manufacturer Information
This product is manufactured by:
BHM Medical Inc.
2001 Tanguay Street
Magog (Quebec)
Canada J1X 5Y5
Authorized European Representative
Huntleigh Healthcare Ltd.
310-312 Dallow Road
Luton, UK
LU1 1TD
General Information
4
Definitions Used in this Manual
WARNING:
Means: Failure to understand and follow
these instructions may result in injury to
yourself and others.
CAUTION:
Means: Failure to follow these instructions
may cause damage to the product.
NOTE:
Means: This is important information
regarding the correct use of the equipment.
Intended Use
Ministand™ is a mobile passive lift with a
Safe Working Load (SWL) of 160 kg (350
lb), intended to be operated on horizontal
surfaces for lifting and transferring in
hospitals, nursing homes or other health care
facilities where the patient:
Sits in a wheelchair;
Is able to partially bear weight on at least
one leg;
Has some trunk stability;
Is dependant on caregivers in most
situations;
Is physically demanding for caregivers;
Has a significant need for the stimulation
of his/her remaining abilities.
The Ministand™ is only for transferring
patients. It is to be used for patients within the
specified weight limit indicated on the lift and
the specified environmental conditions
described in this manual.
The Ministand™ must always be handled by a
trained caregiver, who must attend the patient
during lift application and operation, and in
accordance with the instructions outlined in
this Instructions for Use.
The Ministand™ is intended to be used with
loop slings (compatible with two-hook
spreader bars). Use only slings that are
designed for the Ministand™.
WARNING: Before attempting to use the
Ministand™, a full clinical assessment of the
patient’s condition and suitability for
transfer must be carried out by a qualified
person.
CAUTION: It is not recommended to use
the lift and mount the charger in humid,
salty, oxidizing and/or chlorinated
conditions. In such cases, a proactive
regiment of frequent inspections and
maintenance should be carried out.
Any references to “the patient” in this
document apply equally to a resident at home
or in a long term care facility and refer to the
person being lifted or transferred.
References to left or right in these instructions
are as viewed from the caregiver’s pushing
position, standing at the rear of the
Ministand™, facing forward.
Figure 1
WARNING: Always maneuver the lift using
the handles in the travel direction indicated
on Figure 1 and with the base legs closed.
Left
Right
General Information
5
Operational Life
The equipment is designed and tested for a
useful life of seven (7) years or
10 000 transfers—whichever comes first—
subject to preventative maintenance as
specified in the “Disinfection, Cleaning and
Maintenance” section in this manual. Time
equivalence between the number of transfers
versus the number of years is made clear in
the table below.
Transfers per Day Years
(10,000 transfers)
4 7
6 4.5
8 3.5
WARNING: The manufacturer cannot ensure
full safety for a floor lift or an accessory of
which the life span has been exceeded.
The operating life of this equipment
corresponds directly to the safe operating time
period before a complete overhaul is required.
Aging of the unit, frequency of use (transfers
per day), the weight of the patient and
maintenance frequency are factors that have
an impact on the lift’s life span. A transfer is
defined as the displacement of a patient from
one point to another. A transfer cycle includes
a lifting and a descending action.
The expected life for other consumable
products, such as batteries, fuses, lamps,
slings, straps and cords is dependent upon the
care and usage of the equipment concerned.
Consumables must be maintained in
accordance with published Instructions for
Use and the “Preventive Maintenance
Schedule”.
Equipment Identification
The unit's identification number
(specification, model, serial number) appears
on a silver nameplate attached to the lift’s
mast.
Verifying the Package Contents
Upon receipt of the equipment, verify it
against the packing list to ensure it is
complete and inspect the equipment for
possible damage due to shipping. If there is
any damage, notify the carrier immediately to
file a claim. Provide complete information
concerning damage claims or shipping errors
to your local BHM Medical representative.
Include all equipment identification numbers
and group part numbers (if any) as described
above along with a full description of
damaged parts.
Policy on Number of Staff Members
Required for Patient Transfer
BHM Medical’s passive and active series of
lifts are designed for safe usage with one
caregiver. There are circumstances, such as
combativeness, obesity, contractures etc. of
the patient that may dictate the need for a
two-person transfer. It is the responsibility of
each facility or medical professional to
determine if a one or two person transfer is
more appropriate, based on the task, patient
load, environment, capability, and skill level
of the staff members.
General Information
6
Symbols Used
Symbols Key to Symbols
This symbol is accompanied by the name and the address of the
authorized representative in the European Community.
This symbol is accompanied by a date to indicate the date of
manufacture and by the address of the manufacturer.
This symbol indicates the product complies with all the applicable
European Directives.
This symbol is accompanied by the product’s number of the
manufacturer.
This symbol is accompanied by the product’s serial number of the
manufacturer.
This symbol indicates “separate collection” for all batteries as per the
WEEE Directive. The black bar indicates the equipment was first
placed on the market after August 13th 2005.
This symbol indicates a reference to the Instructions for Use.
This symbol indicates a class II equipment: term referring to
electrical equipment in which protection against electric shock does
not rely on basic insulation only.
This symbol indicates a type B applied part.
This symbol indicates a risk of pinching.
This symbol indicates the maintenance indicator light.
Safety Instructions and Warnings
7
Safety Instructions and Warnings
The equipment must be used in accordance
with these safety instructions.
Anyone using the equipment must also have
read and understood the instructions in this
manual or serious injury may result.
If there is anything you are not sure about,
contact your local BHM Medical
representative.
WARNING: Only manufacturer designated
parts designed for the purpose must be
used for the Ministand™, in order to avoid
injuries attributable to the use of inadequate
parts.
WARNING: Unauthorized modifications or
repairs on the Ministand™ may affect its
safety and invalidate any warranty. The
manufacturer will not accept responsibility
for any accidents, incidents or lack of
performance that occur as a result of any
such unauthorized modification or repair.
General Instructions
Keep the “Safety Instructions” with the floor
lift at all times.
Read the Instructions for Use in this manual
before installing, operating or servicing this
equipment.
WARNING: BHM Medical mobile floor lifts
are specifically designed for BHM Medical
slings and accessories. Slings and
accessories designed by any other
manufacturer are prohibited and will void
BHM Medical’s warranty. Use only BHM
Medical slings and accessories to maintain
patient’s safety and product utility.
General
Always carry out the “Before Every Use”
inspection checklist prior to transferring a
patient.
This mobile patient lift must be operated
by a trained attendant. Do not attempt to
use the lift if you have not been properly
trained to do so. This patient lift should
never be used by patients on their own.
Never use a damaged, torn or frayed sling.
Do not use a sling that is not
recommended for the lift
This mobile floor lift is intended to be
used for patients within the specified
weight limit indicated for the lift. Do not
lift more than the weight limit indicated.
Follow lifting procedures outlined in this
manual.
Never leave a patient unsupervised during
a transfer.
Always place the sling around patient
according to the sling instructions.
Always maneuver the lift by using the
handles located on the mast. If necessary,
initiate the movement by pushing on the
back of the base with your foot. Never
push on the legs.
Do not attempt to maneuver the lift by
pushing on the mast, motor shaft, boom or
patient.
Do not use, in any way, the actuator as a
handle to push or pull the lift. If the
actuator is used as a handle, attendant and
patient safety is greatly compromised.
Replace any precautionary or instruction
labels that cannot be easily read.
Do not store the lift in a shower, bath or
other area with high humidity.
Do not use an electric lift in a shower.
Your lift is for transferring patients only.
Do not use the lift for any other purpose.
Do not attempt to push or pull a loaded lift
over a floor obstruction which the castors
are unable to ride over easily, including
steps, door thresholds or moving sidewalk.
This mobile floor lift is not intended to be
used on an inclined surface.
Safety Instructions and Warnings
8
Do not push the lift at a speed which
exceeds a slow walking pace (3 km/hour
or 0.8 meter/second).
Do not bump the lift down steps whether
loaded or not.
Do not push the lift over uneven or rough
ground, particularly if loaded.
Avoid any impact during transfer.
While the base of the lift can be opened to
ease transfer of a patient, it should be kept
closed between transfer points.
Do not put fingers, hands or feet where
space is limited (see Fig. 2). This could
pinch, cut, or seriously harm body parts.
This includes spaces between the lift base
and floor (1), between lift base and shifter
system (2) between actuator cab and mast
tubing (3) and between actuator and
control box (4).
Figure 2
CAUTION: Keep all components of the lift
clean and dry, and have electrical and
mechanical safety checkpoints performed as
instructed in the “Disinfection, Cleaning and
Maintenance” section of this manual.
WARNING: Do not overload the Ministand™
beyond the approved lifting capacity of the
lowest rated attachment/accessory. If the
maximum load differs between hoist,
spreader bar and body support unit (i.e.
sling), then the lowest maximum load must
always be used.
Electric Shock Prevention
Read the battery and charger instructions
thoroughly before using or storing them.
Do not touch or use a lift with bare wire
conductors or a damaged power cord.
Electrically live equipment can result in
serious injuries. If the lift or charger has any
exposed or damaged wires, contact your local
BHM Medical representative immediately.
Do not splash or expose electric parts of the
device to water or moisture.
Check nameplate for input voltage and
frequency requirements. These requirements
differ by country. Do not attempt to use the
lift in an area that has a different voltage and
frequency requirement.
Do not attempt to expose, service or repair
the lift, battery or charger. If any unit is
malfunctioning, contact your local
BHM Medical representative.
Fire and Explosion Prevention
WARNING: Do not place or store the battery
under direct sunlight or near a heat source.
Do not expose the batteries. Do not charge
the lift in the presence of flammable
anesthetic gases.
Do not short circuit the battery terminals.
Do not incinerate the battery or dispose of in
fire.
Safety Instructions and Warnings
9
Human and Environmental Safety
Practices
Batteries may explode, leak and cause
personal injury if not disposed of properly.
Should the battery casing crack, allowing its
contents to come into contact with skin or
clothing, rinse immediately with water. If the
contents comes in contact with the eyes, rinse
immediately with plenty of water and seek
medical attention.
Inhalation of the contents can cause
respiratory irritation. Sensitivity to nickel can
cause allergic asthma to result. Seek out fresh
air and medical attention.
For recycling and disposal of the batteries, the
rules according to the WEEE directive (Waste
of Electronic and Electrical Components) as
well as local laws and regulations must be
followed. If not, they may explode, leak and
cause personal injury.
When returning batteries, insulate their
terminals with adhesive tape. Otherwise, the
residual electricity in used batteries may cause
fire or explosion. Figure 3 below shows the
symbols for disposal and recycling.
Figure 3
Battery Safety Practices
Be careful not to drop the batteries.
Do not store batteries at a temperature higher
than 50ºC (122ºF).
Do not charge the lift in an unventilated area.
Do not crush, puncture, open, dismantle or
otherwise mechanically interfere with the
batteries.
Equipment Warning Labels
Carefully read the labels on the battery and
follow the instructions.
Inspect all precautionary labels on the
equipment. Order and replace all labels that
cannot be easily read.
Sling Compatibility
10
Sling Compatibility
For more information about sling use, please refer to the documentation that comes with your sling.
Chest sling
(4001C-4001) Total Transfer sling
(4000TTC-4000TT)
Band sling
(TST–X)) Hygienic sling
(THY–X)
Operating the Ministand
11
Operating the Ministand
Introduction
WARNING: Carefully read the “Safety
Instructions and Warnings” section before
attempting to use the lift.
Always carry out the “Before Every Use”
checklist prior to transferring a patient.
NOTE: The Ministand™ should not be used
in conjunction with any patient slings other
than the manufacturer slings which are
expressly designed for the system. The
manufacturer disclaims any responsibility
for improper use employing any other
sling.
NOTE: Instructions provided here are
described from the attendant’s point of
view (i.e. when positioned behind the lift
and ready to move the patient).
Adjusting the Width of the Legs
The base of the lift can be set with the legs
opened or closed. Adjustments are made
according to the various base models:
Shifter base: The adjustments are
made by changing the position of the
shifter: Disengage the shifter plate by
pulling the shifter arm towards you.
Then push the shifter arm to the far
left to close the legs or push it to the
far right to open the legs. (Fig.4)
Pedal base: The adjustments are made
by changing the position of the pedal.
Press down on the left side of the
pedal to close the legs. Press down on
the right side of the pedal to open the
legs (Fig 5).
Power base: The adjustments are
made by using the OPEN and CLOSE
control buttons on the control box or
on the hand control. (Fig.6)
Since the patient’s centre of gravity is
positioned over the centre of the chassis, in
most situations the patient can be comfortably
moved with the base closed. Keeping the
patient at the lowest point within the base
lowers the centre of gravity, increasing patient
security. The patient’s lateral movement is
also reduced by the design of the spreader bar.
WARNING: In manually operated lifts
(shifter and pedal bases) the position of the
legs must be set fully in either the opened
or closed position. Do not position the legs
between these two points, or the legs may
move freely.
Figure 4
Figure 5
WARNING: In power operated lifts (power
base) the position of the legs must be set
fully in either the opened or closed position.
Do not position the legs between these two
points.
With shifter
base
With pedal
base
Operating the Ministand
12
Figure 6
Power Base Models
The base of the lift can be set with the legs
opened or closed by using the two buttons on
the hand controller or by utilizing the
auxiliary buttons located on the panel. (Fig. 7)
Close
Open
Figure 7
Correct Use of the Brakes
Foot operated brakes are fitted on both rear
casters.
Brakes should only be used in the following
situations:
When floor lift unit and patient are
momentarily at rest, for example, during
preparation for transferring to a bed or a
chair.
Whenever movement of the unit has to be
halted while moving a patient.
Upon stationing the lift in front of the
patient, before the patient places his/her
feet onto the footrest.
Brakes application and release:
To apply brakes, step on the back portion
of pad. (Fig 8)
To release brakes, step on the front portion
of pad or lift with toe of shoe. (Fig. 9)
Figure 8 Figure 9
Emergency Shut-Off
The attendant can shut off the electrical power
at any time by pressing the red mushroom
shaped emergency button on the control box.
The button is reset by a half-turn clockwise in
the direction of the arrows.
First time attendants should practice the shut-
off maneuver before operating the lift with a
patient. (Fig. 10)
Figure 10
Emergency
Shut-Off
Button
With power
base
Operating the Ministand
13
Battery Pack
The battery pack is medically approved
according to IEC 60601-1, CAN/CSA-C22-2,
No.601-1 M90 and UL 2601-1.
The battery pack assembly is two 12 volt,
5 Ah (24 volt capacity) fuse protected
batteries, delivering up to 100 lifts per charge
(200 lbs or 90 kg).
Battery life is variable (2-3 years) and is
influenced by proper charging practices and
load exertion.
Removable Battery Pack
The removable battery pack reduces the time
your lift is out of service because of a
discharged battery.
To remove discharged battery pack, use both
hands, grasp the battery pack by the handles
and at the same time, push the two latch
buttons located on each side of the battery
pack, and pull straight out towards you.
Replace the pack with a fully charged one
(second battery pack not included) from the
wall mounted charging unit (not included).
(Fig 11)
Figure 11
NOTE: to ensure long battery life charge for
a minimum of 8 hours before using the lift
for the first time.
Charging the Battery
Plug the charger into a wall socket compatible
with universal voltage input of 90 V up to 240
V. (Fig. 12)
Figure 12
The charger has two LED indicators; yellow
and green. Their significance is:
Green light “ON” with no battery pack
inserted: indicates the charger is on and
ready for use.
Green & Yellow light “ON”: indicates the
battery pack is being charged.
Green light “ON”/Yellow light “OFF”
with battery pack inserted: indicates pack
in the charger is fully charged and ready to
use. (Fig. 13)
Figure 13
WARNING: DO NOT operate the charger with
a damaged cord or if the unit’s housing has
been damaged.
DO NOT forcibly bend the power cord or
place a heavy object on it. This will damage
the cord and may cause a fire or electrical
shock.
Charger
Battery
Operating the Ministand
14
Maintenance Indicator
The maintenance indicator will light after 16
hours of operation (approx. 4000 up/down
cycles). A complete inspection must then be
performed by a qualified technician and a
proper maintenance done according to
findings to prevent accidents. Otherwise, after
19 hours of operation, the indicator will also
emit an audible intermittent beep until the
counter is reset.
Raising and Lowering the
Patient
The electrical actuator operates in both
directions and allows the attendant to raise or
lower the patient without any physical effort.
The hand control can be used to operate the
lift while at the same time the attendant
moves to a position where they can be with
the patient continuously (Fig. 14).
UP
DOWN
Figure 14
To raise the patient:
Touch the “UP” button on the hand control.
Keep your finger on the button until the client
is at the desired height, release finger pressure
and the unit stops.
To lower the patient:
Touch the “DOWN” button on the hand
control. Keep your finger on the button until
the patient is at the desired height, release
finger pressure and the unit stops.
Auxiliary “UP” and “DOWN” buttons are
located on the control box attached to the
mast.
These controls serve two functions:
They are secondary controls in the event the
hand control stops functioning or if two
attendants are involved in the transfer, one
can use the auxiliary controls while the other
moves into a position where they are
continuously with the patient. (Fig. 14)
Active Sling Installation
WARNING: Do not use the band sling on a
patient who does not have good shoulder
and neck muscle-tone.
Check with the patient’s physician, nurse
or medical specialist before using this
sling with a patient
In this manual, the TST sling model is used to
show the basis of an active sling installation.
However, other sling models are available and
are shown in the “Sling Compatibility”
section.
For more information about sling use, please
refer to the Loop Sling Instruction for Use that
comes with your sling.
1. Lean patient forward in the chair and
make sure the patient is supported.
2. With the white PVC material of the sling
facing the patient, place the sling
approximately halfway down the patient’s
back, so that the sling is below the
shoulder blades. Lean the patient against
the back of the chair.
3. Fold the fabric waist band with the Velcro
and belts attached across the mid-section
of the patient. Velcro the belt into place,
then clip the belts closed. Make sure the
buckle is secure (Fig. 15-17).
Operating the Ministand
15
Figure 15
Figure 16
Figure 17
4. Tighten the belt until snug by pulling
gently on the end of it.
Attaching the active sling to
the Ministand
Make sure the sling is correctly installed
around the patient waist (as previously
shown).
Choose the appropriate loop colour according
to the patient needs. Install it into the hooks of
the Ministand™ arm.
Make sure the colour of both loops is the same
on both hooks.
Make sure the loops of the sling are correctly
installed in the hook (Fig. 18). If they are not,
install the loop properly before lifting the
patient.
Figure 18
Ensure the patient’s arms are over the sling
and that the sling is not caught on any
obstructions (e.g. Wheelchair brake or
handle). See figure 19.
Figure 19
Transferring the Patient
Before Lifting the Patient:
1. Lower the boom using “DOWN” button to
its lowest point.
2. Bring the lift towards the patient so that
the Ministand™ footrest is right in front
of the patient's feet.
3. Gently place the patient's feet on the
footrest and push the lift until the patient's
shins are touching the pads.
4. Lock the rear wheels on the Ministand™.
Operating the Ministand
16
5. Place the sling loops on the Ministand™
arm hooks according to the sling’s
instructions. The patient's arms must be
over the sling, and the patient must hold
onto the arms of the Ministand™.
6. Press the “UP” button to raise the patient
slightly. Check to make sure that there are
no obstacles in the way. If you find that
the sling has loosened a bit around the
waist of the patient, tighten the belts
around the patient’s waist. Once the
patient is secure, continue to raise the
patient until he/she is above the chair or
toilet before moving to the next transfer
point.
NOTE: For increased comfort, instruct the
patient to let himself/herself lie back in the
sling during the transfer.
7. Move the patient directly over the point of
transfer and lock the wheels on the
wheelchair or bed. When the patient is
positioned against the chair or bed, lock
the rear wheels on the Ministand™.
8. Slowly lower the patient by pressing the
“DOWN” button. As you lower the
patient, use the handles on the back of the
sling to position the patient in the chair.
9. Lower the arms of the Ministand™ to its
lowest point.
10. Remove the sling straps from the arms of
the Ministand™.
11. Lift the patient's feet off the foot rest and
move the lift a few inches away from the
patient. Sling may be removed from
around the patient.
Main Actuator Failure
In case of a main actuator failure, position the
lift where the patient may be lowered and
with the help of a second attendant, support
the patient, detach the sling and set the patient
down on a bed or chair.
Disinfection, Cleaning and Maintenance
17
Disinfection, Cleaning and Maintenance
Lift Cleaning and Care
WARNING: It is recommended that your
Ministand™ and its accessories are regularly
cleaned and/or disinfected between each patient
use if necessary, or daily as a minimum. If the lift
and/or equipment needs cleaning, or is
suspected of being contaminated, follow the
cleaning and/or disinfection procedures
recommended below, before re-using the
equipment.
For cleaning your lift, equipment and
accessories wipe down with a damp cloth using
warm water to which a disinfectant/cleaner has
been added.
CAUTION: Do not over wet areas of the product
which could cause problems with electrical
components or internal corrosion. If a hot air
dryer is used to dry the lift, the temperature must
not exceed 80°C (176°F.) Do not use petroleum
based solvents or similar, since this may damage
plastic parts.
For disinfection of contaminated lifts, equipment
and accessories, use the preferred method of
wiping the product completely with “hard
surface disinfectant wipes” that are supplied
impregnated with a 70% v/v solution of
Isopropyl Alcohol.
Rub the unit vigorously when using the wipes, to
promote effective disinfection of the surfaces.
The Ministand™ is subject to wear and tear, and
the following actions must be performed when
specified to ensure that the product remains
within its original manufacturing specifications.
BHM Sling Maintenance
For more information about sling maintenance,
please refer to the Instruction for Use that comes
with your sling.
Disinfection, Cleaning and Maintenance
18
Maintenance Schedule
The Ministand™ is subject to wear and tear, and the following actions must be performed when specified
to ensure that the product remains within its original manufacturing specifications.
WARNING: The points on this checklist are the minimum the manufacturer recommends. In some cases
more frequent inspections should be carried out. Continuing to use this equipment without conducting
regular inspections or continuing to use this equipment when a fault is found will seriously compromise
the safety of both the user and the patient. Local regulations and standards may be higher than those of
the manufacturer. Preventive maintenance specified in this manual can prevent accidents.
Refer to diagram on the following page for the location of each inspection area.
These procedures are supplied as a guideline for personnel who are responsible for the maintenance and
safety inspections of patient handling devices. The manufacturer accepts no responsibility for ongoing
inspections and checks. These are guidelines only and are not intended as a substitute for a regular,
thorough equipment maintenance program.
The first inspection must be carried out initially a first time using the lift and then every month.
Note: if during your inspection any bolt, nut or structural fastener is removed, it is imperative that you
reinstall all associated safety devices such as cotter pins, split rings and lock nuts. If one of these devices
is defective, you must replace it with an original new component.
Monthly Inspection
ITEM # PROCEDURE
1 ENSURE THE PIVOT CLEVIS PIN IS WELL SECURED BY THE SPLIT RING AT BOTH END OF
THE ACTUATOR.
2 ENSURE THAT THIS PIVOT SHOULDER BOLT IS SECURELY FASTENED WITH THE
LOCKNUT.
3 CHECK FRONT AND REAR CASTERS REGULARLY FOR HAIR AND DEBRIS, CLEAN AS
NECESSARY, CHECK BRAKE FUNCTION ON REAR CASTERS.
4 INSPECT ALL WELD SITES FOR CRACKING OR SEPARATION.
5 ENSURE ALL NUTS ARE SECURE ON THE STUDS, ENSURE JAM NUTS ARE SECURE ON
SHAFT
6 MAKE SURE THE COTTER PIN IS IN PLACE
7 RUN ACTUATOR FROM LIMIT TO LIMIT TO ENSURE LIMIT STOPS ARE FUNCTIONING.
8 PRESS THE EMERGENCY BUTTON TO ENSURE THAT ALL ELECTRICAL POWER IS CUT
OFF.
9 CHECK ALL THE FUNCTIONS ON THE HAND CONTROL – CHECK TO ENSURE WIRES ARE
NOT PULLED OUT OF CONNECTOR ON HAND CONTROL CASE.
10 CHECK FOR THE SMOOTH FUNCTION OF THE UP/DOWN SWITCHES.
11 CHECK BATTERY PACKS FOR DAMAGE – CHECK THAT THEY WILL ACCEPT A CHARGE BY
PUTTING THEM IN THE CHARGER.
12 CHECK THE FUNCTION OF THE CHARGER LIGHTS (ON THE LIFT OR ON WALL CHARGER)
BY INSERTING A BATTERY PACK – ENSURE THAT POWER LIGHT IS FUNCTIONAL.
13 CHECK THAT THE SAFETY LATCHES ARE IN PLACE AND FUNCTIONAL.
14 MAKE SURE BOTH LEGS ARE PARALLEL
Checklist Before Use
Always perform the following checklist before attempting to transfer a patient:
Ensure that the safety latches are present and are freely pivoting.
Disinfection, Cleaning and Maintenance
19
Ensure that the low battery indicator is not flashing when operating the lift.
Ensure that the footrest is correctly attached to the mast
Ensure that the kneepad is in the proper position for the patient.
Ensure that the kneepad is tightened.
If the product does not work as intended, immediately contact your local BHM representative for support.
Figure 21
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BHM Medical Ministand Instructions For Use Manual

Type
Instructions For Use Manual

BHM Medical Ministand is part of a series of quality products designed especially for hospitals, nursing homes and other health care uses. The device can be used for lifting and transferring a person, and it comes with a variety of features to ensure the safety and comfort of both the patient and the caregiver. Some of the key features of the Ministand include:

  • Adjustable width legs: The legs of the Ministand can be adjusted to accommodate different patient sizes and needs.
  • Power Base Models: The Ministand is available with a variety of power base models to meet the specific needs of your facility.

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