COMPASS HEALTH Richmar DQAPT User manual

1
TABLE OF CONTENT
Foreword................................................................................................ 3
Operator Qualifications ....................................................................... 3
Operator Training................................................................................ 4
Product Description............................................................................. 5
Safety Instructions ............................................................................... 6
Symbols............................................................................................... 6
Precautionary Definitions .................................................................... 8
Warnings and Cautions....................................................................... 9
FCC................................................................................................... 13
Bluetooth®......................................................................................... 14
EMC Guidance..................................................................................... 15
Clinical Instructions ........................................................................... 22
Indications......................................................................................... 22
Contraindications .............................................................................. 22
Adverse Effects................................................................................. 23
Technical Specifications.................................................................... 24
Working Principle ............................................................................... 26
Inspection of the Goods..................................................................... 27
Unpacking the Unit............................................................................ 27
Inspections........................................................................................ 27
Overview of the Unit........................................................................... 29
Nomenclature.................................................................................... 29
Accessories....................................................................................... 30
Interface Introduce ............................................................................. 32
Self-inspection................................................................................... 32
Main Menu Interface .........................................................................33

2
System Setting..................................................................................34
Arm Training...................................................................................... 35
Leg Training ...................................................................................... 46
Spasm Control...................................................................................47
Emergency Stop................................................................................47
Fine Motor Training...........................................................................48
Pause and End of Training................................................................50
Training Data Summary ....................................................................50
Favorites Interface ............................................................................ 51
Training Date Export ......................................................................... 53
Operation Guidance ........................................................................... 54
Preparation before Training .............................................................. 54
Use Heart Rate Sensor.....................................................................54
Secure Patient Position and Adjust Trainer ...................................... 55
Interface Operation and Parameter Settings ....................................58
End of Training..................................................................................58
Care and Maintenance........................................................................ 60
Cleaning............................................................................................ 60
Routine Maintenance ........................................................................61
Fuse Replacement............................................................................61
Expected Useful Life Time ................................................................62
Disposal.............................................................................................62
Troubleshooting.................................................................................. 64
Assistance........................................................................................... 66
Warranty .............................................................................................. 67

3
Foreword
Thank you for purchasing DQAPT from our company.
This manual has been written for the owners and operators of the
DQAPT. It contains general information on the instructions for safety,
intended use, working principle, operation, maintenance, trouble
shooting, and warranty. In order to maximize the use, efficiency, and
working life of your unit, please read this manual thoroughly and become
familiar with the controls, as well as the accessories, before operating
the unit. This manual contains general safety, working principle,
operation, protocols guidance, maintenance, and trouble shooting for
the owners and operators of the DQAPT.
Specifications put fifth in this manual were in effect at the time of
publication. However, owing to policy of continual improvement by
Compass Health Brands, Corp., any changes to these specifications
may be made at any time without obligation on the part of Compass
Health Brands, Corp.
Before administering any treatment to a patient, the user of this
equipment should read, understand, and follow the information
contained in this manual for each mode of treatment available, as well
as the indications, contraindications, warnings, and precautions.
Operator Qualifications
DQAPT is intended exclusively for use by medical specialists and is only
allowed to be used by qualified and instructed medical persons in a

4
clinical environment. Specialists must have the basic physical and
cognitive prerequisites such as vision, hearing, and literacy. Also, the
basic function of the upper extremities is expected.
Operator Training
Operators of the DQAPT must have been adequately trained in using
this system safely and efficiently before they operate the unit. A
documented, cross-functional review must be performed, as many times
as necessary, in order to ensure that instructions can be understood by
users. The operator must be instructed in the following points:
Instruction in operation and designated use of the instrument with
practical exercises;
Mode of effect and function of the unit;
Settings of all components;
Indications for use of the unit;
Contraindications and side effects of the device;
Explanation of the warning notes in all operating status;
Instructions on how to maintain the unit.
Further training requirements vary from country to country. It is the
operator’s responsibility to ensure that the training meets the
requirements of all applicable local laws and regulations. Other
information about training in the operation of this system can be
obtained from Compass Health Brands, Corp.

5
Product Description
DQAPT is a rehabilitative training device that suitable for the active and
passive movement of a person’s lower and upper extremities. It has four
training modes (STRENGTH, ENDURANCE, SYMMETRY and ROM
training mode) and spasm control function. The device can connect the
heart rate sensor via Bluetooth to real-time display heart rate during
training.
Clinic purpose: Therapeutic and Rehabilitation
Suitable places: Clinic and hospital

6
Safety Instructions
Symbols
1. Symbols on the medical device
Symbols
Explanation
Manufacturer
Date of manufacture
Correct Disposal of This Product (Waste Electrical &
Electronic Equipment) Statement: Contact the local
authorities to determine the proper method of
disposal of potentially bio-hazardous parts and
accessories.
Type B applied part complying with IEC 60601-1
This device emits non-ionizing radiation.
Refer to instruction manual/ booklet

7
2. Symbols on the package
Symbols
Explanation
This side up
The transportation package must be vertical and
straight up during transportation.
Fragile, handle with care
The product inside the packaging could be easily
damaged if dropped or handled without care and
attention.
Keep away from rain
The product package should keep out of the rain and
not to store it in damp conditions.
Temperature limitation
The product package should be stored at a
temperature between -20 and 55 degrees (centigrade).
Upper limit of humidity
The product package should be stored at a humidity
less than 93%.
Atmospheric pressure limitation
The product package should be stored at an
atmospheric pressure between 86kPa and 106kPa.

8
Precautionary Definitions
The precautionary instructions found in this section and throughout this
manual are indicated by specific symbols. Understand these symbols
and their definitions before operating this equipment. The definition of
these symbols is as follows:
Text with a “CAUTION” indicator will explain possible safety infractions
that could have the potential to cause minor to moderate injury or
damage to equipment.
Text with a “WARNING” indicator will explain possible safety infractions
that will potentially cause serious injury and equipment damage.
Refer to Instruction Manual/Booklet
NOTE: Throughout this manual, “NOTE” may be found. These Notes
are helpful information to aid in the particular area or function being
described.
Type B applied part
The LE pedal and calf support combination, the UE pedals, and the
handlebar are considered as one type B applied part.

9
Warnings and Cautions
Please read carefully the user manual before using DQAPT and take
care of what follows:
Read, understand, and practice the precautionary operating
instructions. Know the limitations and hazards associated with
using the DQAPT. Observe the precautionary and operational
decals placed on the unit.
Improper installation, operation or maintenance of DQAPT may
result in malfunctions of this unit or other devices.
To avoid the risk of electric shock, the DQAPT must only be
connected to supply mains with protective earth.
MAINS PLUG is used as the isolation means to isolate form
supply mains. Do not position the product so that it is difficult to
operate the mains plug.
Ensure that the power cord is easily detachable in an emergency
situation.
Take care not to allow water to enter the device. Liquid
penetration could damage the device. Keep cables and electric
components away from water and high humidity.
Do not connect or disconnect the device from plug with wet
hands.
Before you plug the DQAPT into a main socket please check that
the voltage of the device stated on the marking corresponds with
the voltage of the power supply.
Do not press, bend or damage the electric cable.
Avoid connecting more devices to the same multiple plug
(Overheating risk).

10
Do not use in the following circumstance: the mixture of the flammable
anesthetic gas and air; the mixture of the flammable anesthetic gas
and oxygen or nitrous oxide, or other flammable agents.
In case of display failure or other obvious defects, switch the
device off immediately, and notify a certified service technician.
Adjustments or replacement of components may result in the
equipment failing to meet the requirements for interference
suppression.
Use the device only for the intended purpose as defined in this
manual
If experiencing any pain, nausea, circulatory weakness, the
training should be stopped right away and your doctor should be
consulted.
During training, if the motor is out of control, please press the
emergency stop button immediately to stop training.
Please stop the device if there is abnormal circumstance during
the process of the training. If the device smokes please press the
OFF button and turn it off, disconnect the power cord and contact
with the distributor as soon as possible.
No modification of this equipment is allowed.
Prior to replace the fuse of the device, make sure that the device
is turned off and the power cord has been disconnected.
Do not remove the covers. This may cause unit damage,
malfunction, electrical shock, fire, or personal injury.. If a
malfunction occurs, discontinue use immediately, disconnect the
Mains Power Cord from the outlet, and contact the after-sale
service department of COMPASS for service.
Never perform unauthorized service work. All service work must
be performed only by service technicians who have been
authorized by the manufacturer.
Do not perform maintenance when the patient uses the unit.

11
During the process of operation, constantly watch patients and
instrument case, always pay attention to whether the abnormal
conditions occur.
Please pull the plug before move the device and try to avoid
vibration during moving the device.
If the device has not been used for a long time (≥2 weeks), please
check and make sure the device and accessories are in good
conditions before use.
The DQAPT should be kept out of the reach of children.
Do not use this device on infants or people not capable of
expressing their intensions. May cause an accident or ill health.
Do not use this device in places with high-intensity magnetic field ,
electromagnetic wave and impulse voltage.
Do not use this device in places with corrosive gas and sunlight.
Do not use this device in places with chemicals.
Please make sure all the electrical cables are connected correctly
and safe before use.
Pay attention that your feet have enough space while adjusting
the arm trainer in height. When using the leg trainer, the legs must
not collide with the arm trainer.
Before starting your training, make sure that the supporting
module of the handlebar or the arm trainer is tightened and that
your legs or arms are secured properly.
Ensure before each training session that the screws of all
adjustable parts of the device (handlebar, supporting module, calf
support) are tightened and intact. In case they get loose during
the operation you have to stop the training immediately and
tighten the screws.
Suitable clothing must always be worn. Wide trousers, long towels

12
and scarves that could get caught or tangled in pedal crank must
not be worn (especially during leg training). Shoes with shoe laces
must not be worn, either.
Before starting leg training, the arm trainer has to be swiveled
back so that the patient can hold on the handlebar.
Before each leg training, you must check whether the patient’s
feet are in the correct position on the LE pedals and have been
secured with straps.
Only put patient’s feet into the LE pedals while seated. Do not put
patient’s feet into the LE pedals while standing. Hands are not
allowed into the LE pedals.
While the pedals are moving, you should not make any
mechanical adjustments to the device. Never try to grab hold of
any moving parts.
Please train only after you have switched on the DQAPT.
The device performs a self-check when it is turned on or release
emergency stop. DO NOT approach the movement area of the
ARM and LEG trainer of the device.
Please avoid the excessive vibration of the device, and operate
the touch screen should be gently.
The training parameters should be set by the doctor or under the
doctor’s the professional guidance.
Do not exceed 20 minutes in the first training.
Do not clean the main unit with organic solvent such as gasoline
or diluents, otherwise damage will be happened to the main unit
such as deformation and falling off of the paint.
Clean the device using a dry soft cloth. Do not use cleaning
solvents or other chemical substances in order to avoid any
damages.
Do not use bleach to clean the straps. Do not put the straps under
high temperature or high pressure to sterilize.

13
Please dispose of the equipment and other accessories according
to local regulations.
FCC
Changes or modifications not expressly approved by the party
responsible for compliance could void the user’s authority to operate the
equipment.
This equipment has been tested and found to comply with the limits for a
Class B digital device, pursuant to Part 15 of the FCC Rules. These
limits are designed to provide reasonable protection against harmful
interference in a residential installation. This equipment generates, uses
and can radiate radio frequency energy and, if not installed and used in
accordance with the instructions, may cause harmful interference to
radio communications. However, there is no guarantee that interference
will not occur in a particular installation.
If this equipment does cause harmful interference to radio or television
reception, which can be determined by turning the equipment off and on,
the user is encouraged to try to correct the interference by one or more
of the following measures:
-- Reorient or relocate the receiving antenna.
-- Increase the separation between the equipment and receiver.
-- Connect the equipment into an outlet on a circuit different from
that to which the receiver is connected.
-- Consult the dealer or an experienced radio/ TV technician for
help.
FCC ID: 2AXDGDQAPT

14
This device complies with Part 15 of the FCC Rules. Operation is
subject to the following two conditions:
1) this device may not cause harmful interference, and
2) this device must accept any interference received, including
interference that may cause undesired operation.
Bluetooth®
The Bluetooth®word mark and logos are owned by the Bluetooth SIG,
Inc. and any use of such marks by Compass Health Brands, Corp. is
under license.
Communication between the device and the heart rate sensor is via
Bluetooth.
Bluetooth Specifications:
Bluetooth Version: 4.0
Frequency Range: 2.402 GHz - 2.48 0GHz
Modulation Type: GFSK
Effective Radiated Power: 0 dBm
Quality of Service (QoS)
Throughput: > 6.4Kb/s
Latency: < 500ms
Packet Error Rate: <10%

15
EMC Guidance
The DQAPT needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided.
This device has been thoroughly tested and inspected to assure proper
performance and operation.
Do not use the DQAPT simultaneously with other therapeutic
device (such as microwave), to avoid mis-operation.
Do not place or use the DQAPT nearby radio, television, copy
machine and fax machine.
Keep the DQAPT away from active HF surgical equipment and
the RF shielded room of a medical device for magnetic resonance
imaging, where the intensity of EM disturbances is high.
Use of the DQAPT adjacent to or stacked with other equipment
should be avoided because it could result in improper operation. If
such use is necessary, this equipment and the other equipment
should be observed to verify that they are operating normally.
Portable RF communications equipment (including peripherals
such as antenna cables and external antennas) other than the
specified heart rate sensor to be used with the DQAPT should be
used no closer than 30 cm (12 inches) to any part of the DQAPT,
including cables specified by the manufacturer. Otherwise,
degradation of the performance of this equipment could result.
Use of accessories, transducers and cables other than those
specified or provided by the manufacturer of the DQAPT could
result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in improper
operation.

16
Cable Information:
Item
Cable Length
Manufacturer
Power cord
2.5 m
Ching Cheng Wire Material Co., Ltd.
Guidance and manufacture’s declaration – electromagnetic
emission
The DQAPT is intended for use in the electromagnetic environment
specified below. The customer of the user of the DQAPT should
assure that it is used in such an environment.
Emission test
Compliance
Electromagnetic
environment –guidance
RF emissions
CISPR 11
Group 1
The DQAPT use RF energy
only for its internal function.
Therefore, its RF emissions are
very low and are not likely to
cause any interference in
nearby electronic equipment.
RF emissions
CISPR 11
Class A
The DQAPT is suitable for use
in all establishments, other than
domestic and those directly
connected to the public
low-voltage power supply
network that supplies buildings
used for domestic purposes.
Harmonic
emissions
IEC 61000-3-2
Class A
Voltage
fluctuations/ flicker
emissions
IEC 61000-3-3
Complies

17
Guidance and manufacture’s declaration – electromagnetic
immunity
The DQAPT is intended for use in the electromagnetic environment
specified below. The customer or the user of DQAPT should assure
that it is used in such an environment.
Immunity
test
IEC 60601
test level
Compliance
level
Electromagnetic
environment -
guidance
Electrostatic
discharge
(ESD)
IEC
61000-4-2
±8 kV contact
±2,4,8,15 kV
air
±8 kV contact
±2,4,8,15 kV
air
Floors should be wood,
concrete or ceramic tile.
If floor are covered with
synthetic material, the
relative humidity should
be at least 30%.
Electrical
fast
transient/
burst
IEC
61000-4-4
±2 kV for
power supply
lines
±1 kV for
input/output
lines
±2 kV for
power supply
lines
Mains power quality
should be that of a
typical commercial or
hospital environment.
Surge
IEC
61000-4-5
±0.5kV, ±1
kV line(s) to
lines
±0.5kV, ±1
kV, ±2 kV
line(s) to
earth
±0.5kV, ±1
kV line(s) to
lines
±0.5kV, ±1
kV, ±2 kV
line(s) to
earth
Mains power quality
should be that of a
typical commercial or
hospital environment.
Voltage
dips,short
interruption
0% UT; 0.5
cycle (0°,45°,
90°,135°,180
0% UT; 0.5
cycle (0°,45°,
90°,135°,180
Mains power quality
should be that of a
typical commercial or

18
sand
voltage
variations
onpower
supply
inputlines
IEC
61000-4-11
°,225°,270°
and 315°)
0% UT; 1
cycle and
70% UT;
25/30 cycles
Single
phase: at 0°
0% UT;
250/300
cycles
°,225°,270°
and 315°)
0% UT; 1
cycle and
70% UT;
25/30 cycles
Single
phase: at 0°
0% UT;
250/300
cycles
hospital environment. If
the user of the DQAPT
requires continued
operation during power
mains interruptions, it is
recommended that the
DQAPT be powered
from an uninterruptible
power supply or a
battery.
Power
frequency
(50/60Hz)
magnetic
field IEC
61000-4-8
30 A/m
30 A/m
Power frequency
magnetic fields should
be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment.
NOTE UTis the a.c. mains voltage prior to application of the test
level.