Arjo AtmosAir Velaris User manual

INSTRUCTIONS FOR USE
AtmosAir Velaris
Hybrid mattress system
04.AAV.00EN_02 • 10/2021

2
Design Policy and Copyright
® and ™ are trademarks belonging to the Arjo group of companies.
© Arjo 2021.
As our policy is one of continuous improvement, we reserve the right to modify designs without prior notice.
The content of this publication may not be copied either whole or in part without the consent of Arjo.
WARNING
To avoid injury, always read this Instructions for use and accompanied documents
before using the product.
Mandatory to read the Instructions for use.

3
Contents
Foreword . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
Safety instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Parts designation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Control panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Run/Standby button and light . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Lock button and light. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Audio offlight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Weight select buttons and lights . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Audio alarm pause button and light . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Power fail light. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
System fault light. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Low pressure light. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Skin IQ light. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Product description - Alternating pressure pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Repeater light . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Hanging brackets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Power cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Skin IQ port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Audio on/offswitch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Day/Night mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Product description - Standard and Plus mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Covers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Mattress connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Connect the pump to the mattress. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Disconnect the pump from the mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Handles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Non-slip base . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Cable management loops. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Product description - Stretcher (ST) mattress . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Covers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Handles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Non-slip base . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Product description - Seat cushion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Covers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Handle. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Non-slip base . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

4
Assemble the hybrid mattress system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Assemble the Standard, Plus and ST mattresses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Reactive therapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Patient position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Active therapy (Standard or Plus mattress) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Patient position . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
System start-up. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Turn-offand remove the pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Store the pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
Homecare use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Cleaning and disinfection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Clean and disinfect . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Care and preventive maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Troubleshooting and alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Technical specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
List of standards and certificates . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
Electromagnetic compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47

5FOREWORD 5FOREWORD
Foreword
Thank you for purchasing the AtmosAir Velaris®hybrid mattress system.
Customer contact information
For questions regarding this product, supplies, maintenance, or other Arjo products and services,
contact Arjo, an Arjo authorised representative or visit www.arjo.com.
Read and fully understand this IFU before using the product
The information in these Instructions For Use (IFU) is necessary for the proper operation and
maintenance of your device. It will help to protect your product and make sure that it performs to your
satisfaction. The information in this IFU is important for your safety. You must read and understand the
IFU to help prevent possible injury. Unauthorised modifications on any Arjo device can affect its safety
and performance. Arjo cannot be held responsible for any accidents or incidents resulting from such
modifications to its products.
Service and support
Routine maintenance before every use or every week (in long-term care) is necessary to maintain
the safety and reliability of the product. See the Care and preventive maintenance section for more
information. If you require further information or spare parts, see Customer contact information.
Serious incident
If a serious incident occurs in relation to this medical device, affecting the user, or the patient, then the
user or patient should report the serious incident to the medical device manufacturer or the distributor.
In the European Union, the user should also report the serious incident to the Competent Authority in
the member state where they are located.
Definitions in this IFU
WARNING
CAUTION
NOTE
Warning means: Safety warning. Failure to understand
and obey this warning may result in injury to you or
others.
Caution means: Failure to follow these instructions
may cause damage to all or parts of the system or
device.
Note means: This is important information for the
correct use of this system or device.

6 INTENDED USE6 INTENDED USE
Intended use
The AtmosAir Velaris hybrid mattress system is intended for use by caregivers1in acute care,
long-term care and home care facilities, including private homes.
The hybrid mattress system is indicated for the prevention and management of pressure injuries. It
should be used as part of an individualised, comprehensive pressure injury protocol. This includes:
repositioning, nutritional support and skin care. The surface should be selected based on full
assessment of the patient needs.
The hybrid mattress system represents one aspect of a pressure injury management protocol. All other
aspects of care should be considered by the healthcare professional.
If existing wounds do not improve, or the patient’s condition changes the overall therapy regimen
should be reviewed by the healthcare professional.
As guidance the system when used in an unpowered reactive mode is indicated for patients that are
deemed to be ‘At Risk’ of a pressure injury. If the system is used in conjunction with the pump, the
patients with a ‘higher risk profile’ may be considered.2
The above are guidelines only and should not replace clinical judgement.
The Standard mattress system is for patients within the weight range of 40 kg (90 lb) to 250 kg (550 lb).
Heavier patients weighing up to 454 kg (1000 lb) should use the Plus (bariatric) mattress system.
The hybrid mattress system should only be used for the purpose specified in this Instructions for Use.
Any other use is prohibited.
1 Caregiver may be a healthcare professional or lay person who operates this medical device.
2 European Pressure Ulcer Advisory Panel, National Pressure Injury Advisory Panel and Pan
Pacific Pressure Injury Alliance. Prevention and Treatment of Pressure Ulcers/Injuries:
Clinical Practice Guideline. The International Guideline. Emily Haesler (Ed).
EPUAP/NPIAP/PPPIA: 2019, Chapter 4 Risk Factors and Risk Assessment

7INTENDED USE 7INTENDED USE
Contraindications
In powered active alternating mode with the pump,- Do not use the hybrid mattress system with
patients with an unstable cervical, thoracic and/or lumbar fracture, cervical traction, and skeletal
traction. For any other conditions that may be complicated by a moving surface, do not use the hybrid
mattress system.
In the non-powered reactive mode without the pump, - It may be possible to use the surface for
patients with unstable cervical, thoracic and/or lumbar fracture, cervical traction, and skeletal traction
if assessed by a healthcare professional as suitable to do so. Ongoing assessment and continuous
monitoring of the patient is advised.
Patient assessment
Facilities should establish regular assessment routines. Caregivers should assess each patient before
using the product. The patient weight must not exceed:
• 250 kg (550 lb) for the Standard mattress
• 454 kg (1000 lb) for the Plus (bariatric) mattress
• 250 kg (550 lb) for the Stretcher (ST) mattress
• 250 kg (550 lb) for the Seat cushion
If the patient does not meet these criteria an alternative medical device/system shall be used.
Expected service life
The expected service life of the AtmosAir Velaris system elements is:
• Mattress – 5 Years
• Seat Cushion – 5 Years
• Pump – 7 Years
The expected service life of this device is subject to preventive maintenance being carried out in
accordance with the instructions for care and maintenance found in this Instructions for Use.

8 SAFETY INSTRUCTIONS
Safety instructions
WARNING
To avoid risks of tripping or strangulation,
always use the cable management for the
power cable.
WARNING
To avoid injury, keep the mains power socket
and plug accessible at all times. To safely cut
offthe pump’s power supply, remove the plug
from the mains outlet.
WARNING
To avoid pressure injury, make sure that
the hybrid mattress system is assembled
correctly.
WARNING
To avoid bodily injury, do not use the
mattress or ST mattress as a patient
movement device.
WARNING
To avoid injury and/or unsafe product, do not
use unapproved accessories or attempt to
modify, disassemble or otherwise misuse the
hybrid mattress system.
WARNING
Do not attempt to service or maintain the
pump while it is in use. CPR
Level the bed and disconnect the Velaris pump (if
connected). Lower the side rails and initiate CPR as
detailed in the facility protocols.
WARNING
To avoid falls and injury, make sure that
cables and the tube-set are positioned
correctly. Keep cables away from moving bed
parts or other possible entrapment areas.
WARNING
To avoid pressure injury the patient must
not wear clothing that may cause areas of
localized high pressure due to creases,
seams, etc. Objects in pockets must be
avoided for the same reason.
WARNING
To avoid reduced benefits from the mattress,
do not place extra layers between the patient
and the mattress.
CAUTION
To avoid damage to the device, do not use
sharp objects or electrical heat under the
blankets on or under the hybrid mattress
system.
CAUTION
To avoid damage, do not expose the device
to naked flames, such as cigarettes. This is
especially important for the mattress. A leak
in the mattress (Standard and Plus) may
propagate the fire.

9PREPARATION 9PREPARATION
Preparation
Bed frame recommendation
The mattress range is designed to be used on Arjo bed frames. See Technical specifications on page
38 of this IFU.
The mattress range (Standard, Plus and ST) may also be used with other bed frames or trolleys
(non-Arjo). The clinician or caregiver should assess the needs and determine which mattress and
bed frame to use. See the bed frame IFU for compatible mattress sizes. Find the dimensions of all
mattresses in section Measurements and compatibility on page 40.
Actions before first use
1. Visually check the package for damage. If the package is damaged, contact the transport agency.
Do NOT use the product.
2. Read this IFU.
3. Check that all parts of the product are supplied: Compare to section Parts designation on page
10. If any part is missing or damaged – do NOT use the product.
4. Recycle the packaging according to local regulations.
5. Choose a designated area where this Instructions for Use should be kept and is easily accessible at
all times.
Actions before every use
Inspect the hybrid mattress system according to section Care and preventive maintenance on page
34. If any item is damaged - do NOT use the product.
Action after each patient
Clean and disinfect the product after each patient according to section Cleaning and disinfection on
page 30.

10 PARTS DESIGNATION
1
5
4
3
2
6
Control panel
Parts designation
1. Run/Standby button and light
2. Lock button and light
3. Audio OFF light
4. Weight decrease button (-)
5. Weight selected light
6. Weight increase button (+)
7. Power fail light
8. Audio alarm pause button and light
9. Low pressure light
10. System fault light
11. Skin IQ connected light
Skin IQ
AtmosAir Velaris
40 60 80 100 130 170 210 250 350 450 kg
154698
1110
732
1. Control panel (with lights)
2. Repeater light
3. Tube-set connector
4. Hanging brackets
5. Skin IQ port
6. Power cable
Alternating pressure pump

11PARTS DESIGNATION
1. Detachable top cover
2. Mattress connector
3. Mattress connector cavity
4. Non-Slip strips
5. Detachable bottom cover
6. Handles
7. Cover attachment zip with zip flap
8. Cable management loops
Standard and Plus mattress
1
7
6
5
2, 3
4
8

12 PARTS DESIGNATION
1
5
4
3
2
1. Detachable top cover
2. Non-Slip strips
3. Detachable bottom cover
4. Cover attachment zip with zip flap
5. Handles
Stretcher (ST) mattress

13PARTS DESIGNATION
1. Detachable top cover
2. Cover attachment zip with zip flap
3. Non-Slip strip
4. Detachable bottom cover
5. Handle
Seat cushion
1
5
4
2
3

14 CONTROL PANEL
Control panel
Run/Standby button and light
See Figure 1
The Run/Standby button switches the pump between
Run mode and Standby mode.
In Run mode the light is on.
For Standby mode, press and hold the button for two
seconds. The light turns off.
Lock button and light
See Figure 2
To lock the control panel, press and hold the Lock
button for 2 seconds. When locked the light turns on.
To unlock all control panel buttons, press and hold
the Lock button for two seconds. When unlocked the
light turns off.
The control panel buttons automatically lock after 60
seconds if no control panel button is pressed.
Audio offlight
See Figure 3
The Audio offlight turns on when the Audio
notifications and alarms have been permanently
disabled.
See Audio on/offswitch on page 18
Figure 1
Figure 2
Figure 3

15CONTROL PANEL
Weight select buttons and lights
See Figure 4
The default weight is set and the light is on at 100 kg
(220 lb).
• Press the - button to reduce the patient weight.
Minimum value is 40 kg (90 lb).
• Press the + button to increase the patient weight.
Maximum value is 450 kg (1000 lb).
For each button press the weight reduces/increases
by one step.
The selected weight is indicated by a green light.
The Plus mattress weight settings (350 kg and 450
kg) are indicated by a blue light when selected.
Always round up the patient’s weight to the next
higher value.
Audio alarm pause button and light
See Figure 5
Press the Audio alarm pause button to silence the
audible alarm for 15 minutes. The light turns on.
Press the button again to cancel the alarm pause.
40 60 80 100 130 170 210 250 350 450
kg
Figure 4
Figure 5

16 CONTROL PANEL
Power fail light
See Figure 6
If a power failure is detected the power failure light
turns on and an alarm sounds.
Active (alternating) therapy is not possible during
power failure conditions.
System fault light
See Figure 7
If an internal fault of the pump is detected during
Built-In Self-Test (BIST) or during therapy, the
system fault light turns on and an alarm sounds
Low pressure light
See Figure 8
If the mattress fails to achieve the target pressure,
the low pressure light turns on and an alarm sounds.
Skin IQ light
See Figure 9
The Skin-IQ light turns on when a Skin-IQ coverlet is
connected to the Skin IQ power outlet port.
See Figure 13.
Figure 6
NOTE
To turn the pump offand cancel the alarm
during a power outage, press and hold the
run/standby button for two seconds.
Figure 7
Figure 8
Skin IQ
Figure 9

17PRODUCT DESCRIPTION - ALTERNATING PRESSURE PUMP
Product description - Alternating pressure pump
Repeater light
See Figure 10
During normal operation the repeater light is on and
green.
During a fault condition, the repeater light will turn
yellow.
Hanging brackets
See Figure 11
Use the hanging brackets to mount the pump at the
foot end of the bed.
The pump can also be placed on a flat surface near
the bed and the mattress connector.
Power cable
See Figure 12
Position the power cable in the cable management
loops on the left side of the mattress.
See Figure 22 on page 21.
Figure 10
Skin IQ
AtmosAir Velaris
40 60 80 100 130 170 210 250 350 454
kg
Figure 11
Figure 12
Skin IQ
AtmosAir Velaris
40 60 80100 130 170 210 250 350 454
kg

18 PRODUCT DESCRIPTION - ALTERNATING PRESSURE PUMP
Skin IQ port
See Figure 13
Only use the Skin IQ port with the Skin IQ power
cable to provide power to the Skin IQ coverlet.
See Allowed combinations on page 39.
For instructions on how to use Skin IQ, see the Skin
IQ IFU.
Audio on/offswitch
See Figure 14
The Audio on/offswitch disables all pump sound
notifications. Use it when it has been determined that
audio output could be disturbing for the patient.
The Audio on/offswitch is located underneath the
side panel cover. The cover can only be removed by
a service technician.
Set the switch to position A to disable all audio
output. Set the switch to position B to enable all
audio output.
Day/Night mode
A light sensor automatically reduces the brightness
of the pump lights in low ambient light.
Figure 13
A
B
Figure 14
NOTE
The Audio on/offswitch should only be used
by qualified personnel under direction of the
responsible organisation.

19PRODUCT DESCRIPTION - STANDARD AND PLUS MATTRESS
Covers
The mattress top and bottom welded covers are
co-joined by a zip.
Mattress connector
The mattress connector is located at the foot end of
the mattress. See Figure 15
The mattress connector is used to connect the
mattress to the pump.
Connect the pump to the mattress
1. Locate the connector at the foot end of the
mattress and pull it out of the pocket slightly.
See Figure 16.
2. Hold the mattress connector in your left hand and
press the connectors together. Make sure that
the pump tube-set connector clicks into place on
both sides (double-click). See Figure 17.
3. Push the connectors back into the cavity and
reposition the zip flap. See Figure 18.
Figure 15
Figure 16
Figure 17
Figure 18
Product description - Standard and Plus mattress

20 PRODUCT DESCRIPTION - STANDARD AND PLUS MATTRESS
Disconnect the pump from the mattress
1. Locate the connector inside the connector cavity,
near the foot end of the mattress. See Figure 19.
2. Firmly squeeze the two buttons on the top and
bottom of the pump connector and pull it away
from the mattress connector. See Figure 20.
3. Push the mattress connector back into the
connector cavity. See Figure 21.
Figure 19
Figure 20
Figure 21