Hovertech HoverJack User manual

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HOVERJACK® Introduction .................................04
General System Information
AIR SUPPLY ........................................................... 17
Table of Contents
Part Identification - Air Patient Lift ........................................ 05
Part Identification - Air Supply .................................................. 06
Air Supply Keypad Functions .................................................. 07
Instructions for Use ............................................................ 08
Product Specifications/Required Accessories ............................. 09, 10
Electromagnetic Compatibility Chart ......................................... 11 - 14
Cleaning & Maintenance .................................................. 15
Frequently Asked Questions .................................................. 16
Symbol References ............................................................ 02
Intended Use and Precautions .................................................. 03
Components Parts List ............................................................ 28
Warranty Statement ............................................................ 29, 30
Returns and Repairs ............................................................ 31
Part Identification ............................................................ 18
Power Cord / Clamp Replacement ........................................ 19
Handle Replacement ............................................................ 20
Feet or Bumper Replacement .................................................. 21
Hose Removal ...................................................................... 22
Air Filter and Air Filter Cover Replacement ............................. 23
Dust Cover/Hose Attachment Snap Replacement ................... 24
Metal Cover Replacement ................................................. 25
Cord Strap Replacement ................................................. 26
Troubleshooting ..................................................................... 27

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Symbol Reference
Type BF Applied Part
This End Up
Attention! Please read
accompanying documents.
Keep Dry
Temperature
Declaration of Conformity to
Medical Device Directive Humidity
Functional Earth (Ground)
Alternating Current
Date of Manufacture
Underwriters Laboratory Agency Approval
120 V~:
Medical Equipment with respect to electrical
shock, fire and mechanical hazards only in
accordance with UL 60601-1,
IEC/EN 60601-1, CAN/CSA C22.2 No. 601.1
230 V~:
Medical Equipment with respect to electrical
shock, fire and mechanical hazards only in
accordance with UL 60601-1,
IEC 60601-1-2 CAN/CSA C22.2 No. 601.1
~

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Intended Use and Precautions
• Indications:
Patients unable to assist in their own vertical lift, such as after a fall. Patients whose
weight or girth poses a potential health risk for the caregivers responsible for lifting
or moving said patients.
• Contraindications:
Patients who are experiencing thoracic, cervical or lumbar fractures that are deemed
unstable: unless using in conjunction with a spinal board.
• Intended Care Settings:
Hospitals, Long term or extended care facilities
• Precautions:
Make sure Patient Safety Straps are secured before moving.
Never use Patient Safety Straps to pull the HoverJack® air patient lift, as they may tear.
Move the HoverJack® air patient lift using the Transport Straps at the head-end
and/or the handles located along the top perimeter.
When moving a patient on the inflated HoverJack® air patient lift, use caution and
move slowly.
Additional caregivers are recommended when moving a patient over 750 lbs / 340kg.
Never attempt to move a patient on an un-inflated HoverJack® air patient lift.
Route the power cord in a manner to ensure freedom from hazard.
Avoid blocking the air intakes of the air supply.
Never leave patient unattended on an inflated device.
Use this product only for its intended purpose as described in this manual. Only use attachments and
or accessories that are authorized by HoverTech International.
WARNING: For safety, always use a minimum of two caregivers while using the
HoverJack® air patient lift.
CAUTION: Avoid electric shock. Do not open Air Supply.
WARNING: Reference product specific user manuals for additional operating instructions.
HoverJack patient air lift system is not UL classified

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Introduction
Using the HoverJack® Air Patient Lift
In the event of a patient fall, the HoverJack® air patient lift is log-rolled under the
patient. The Hovertech Air Supply is then used to inflate each of the four (4) chambers
to lift the patient in a supine position from the floor to the bed or stretcher height.
This reduces the number of caregivers needed to lift a patient, while minimizing the
potential of further injuries to patient and the staff. The HoverJack® air patient lift
can be used anywhere a patient has fallen, even in confined spaces, such as a
bathroom. The friction-reducing material on the bottom of the patient lift allows
caregivers to easily transport the patient across any surface. The HoverJack® air
patient lift has a weight limit of 1900 pounds / 862 kg and is available in two widths
to accommodate most patients. See the HoverTech International Product Line in the
General System Information section of this manual.
The Principle of the HoverJack® Technology
Recognized as the industry standard for safe patient lifting, the HoverJack® air
patient lift allows caregivers to safely lift patients who have fallen without gathering a
lift team. The HoverJack® air patient lift has four chambers that inflate sequentially to
lift patients from the floor to bed or stretcher height in a supine position, maximizing
patient comfort and minimizing the risk of injury to the patient and their caregivers.
Once the HoverJack® air patient lift is inflated, the HoverMatt® transfer mattress can
be used with the same air supply unit for safe and easy lateral patient transfer to a
bed or stretcher.
The Purpose of the HoverJack® Technology
Consistent utilization of the HoverJack® air patient lift dramatically reduces back
injuries to staff that are caused by manually lifting patients who have fallen.
In addition, fewer staff members are required and the patient is lifted in a very
comfortable manner. When considering Fall Prevention guidelines, the HoverJack®
air patient lift is a critical component of a program that addresses the safety of the
patient and the caregiver if a patient does fall.

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Part Identification - Air Patient Lift
Red Deflate Cap and Valve
(4 Total)
Transfer Handles (8)
Patient Safety Straps (2)
(DO NOT USE TO TRANSFER)
Label Includes:
Model#, Serial# and
Instructions for use.
Inflate Cap and Valve
(4 Total)
Transport Strap

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Part Identification - Air Supply
Air Filter Cover
Hose Nozzle
Hose
Hose Release Button
Control
Panel Label
Carrying Handle/
Attachment Hook
Power Cord
Strap
Power Cord
(US/UK/Euro)

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Air Supply Keypad Functions
The Adjustable Keypad function has four different settings. Pressing the
button once will result in the lowest inflation setting available. A second
press of the button increases the air pressure and rate of inflation. Pressing
the button a third time will again increase the rate of inflation. A fourth press
of the button results in the highest inflation rate and air pressure available
for HoverTech Accessories. The STANDBY button may be pressed at any time
to cease all air flow.
NOTE: The LED will indicate the inflation speed by the number of flashes
(i.e. two flashes equals the second inflation speed).
All of the settings in the Adjustable range are substantially lower than the
HoverMatt® and HoverJack® settings. The Adjustable function is not to be
used for transferring; it is only for use with HoverTech Accessories, which
require a lower pressure for slow inflation.
Standby: Used to stop inflation/air flow.
HoverMatt® 28 /34: For use with 28” & 34” HoverMatt® Air Transfer
Mattresses.
HoverMatt® 39 /50 & HoverJack®: For use with 39” & 50” HoverMatt® Air
Transfer Mattresses and 32” & 39” HoverJack® Air Patient Lifts.
Transfer Speed High
Adjustable/
Pressure Setting
Transfer Speed LowStandby
Power IndicationAdjustable Speed
Indication

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Instructions for Use
1. Place HoverJack® air patient lift on floor next to the patient, making sure the chamber with
Valve #4 is on the top and the chamber with Valve #1 is against the floor.
For safety, always use a minimum of two caregivers when operating the
HoverJack® air patient lift.
2. Make certain that all four red-capped deflation valves are capped tightly to maintain
inflation.
3. Log roll patient onto the deflated HoverJack® air patient lift and position patient with feet at
the valve end where indicated.
4. The patient can be placed on top of the HoverJack® air patient lift using the HoverMatt® Air
Transfer System. (See HoverMatt® instructions). If the HoverMatt® is used, make certain that
the HoverMatt® and patient are properly centered on the HoverJack® air patient lift. Always
deflate the HoverMatt® air transfer system prior to inflating the HoverJack® air patient lift.
Using buckles, secure patient safety straps around the patient.
5. Plug HoverTech International Air Supply power cord into an electrical outlet.
6. Hold hose against inlet Valve #1 of HoverJack® air patient lift.
7. Turn on Air Supply to the highest inflation level to begin inflation with valve #1.
8. When fully inflated, remove hose. Valve will automatically close, keeping chamber inflated.
9. Using the same process, move to Valve #2, Valve #3 and Valve #4 in exact succession.
10.Turn off air supply by pressing standby button and cap valves.
11.Transfer from HoverJack® air patient lift onto adjacent surface using theHoverMatt® air
transfer system. Transfer without the HoverMatt® air transfer system may cause injury.
12.If it is necessary to lower patient down to the floor, release air by opening the uppermost
red deflate valve #4. When chamber #4 is fully deflated, move in succession downward to
fully deflate HoverJack® air patient lift. Caution: DO NOT RELEASE ALL CHAMBERS ALL AT
ONCE.
NEVER LEAVE PATIENT UNATTENDED ON INFLATED HOVERJACK® AIR
PATIENT LIFT.
HOVERJACK®
Use for sizes: 32 & 39

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Product Specifications/Required Accessories
• Classification:
EQUIPMENT NOT SUITABLE FOR USE IN THE PRESENCE OF A FLAMMABLE
ANESTHETIC MIXTURE WITH AIR, OR WITH OXYGEN OR NITROUS OXIDE.
Not for use with Oxygen or Oxygen Enriched Atmospheres.
Type of Protection against electric shock: CLASS I EQUIPMENT
Degree of protection against electric shock: TYPE BF APPLIED PART
Protection against ingress of water: Ordinary (not protected).
Mode of operation: CONTINUOUS OPERATION
To remove supply mains, unplug equipment from wall
• Patient Weight Limit: 1,900lbs / 862kg
• Use Temperature: 50° to 104° F (10° to 40° C)
• Use Humidity: 10% to 70% Non-Condensing
• Storage/Shipping Temperature: -40° to 176° F (-40° to 80° C)
• Storage/Shipping Humidity: 10% to 70% Non-Condensing
• Power Input: 120 V~, 60 Hz, 10 A (North American version)
230 V~, 50 Hz, 6 A (European Version)
• Air Supply Dimensions: 12.5 x 7 x 7 inches (31.75 x 17.8 x 17.8 cm)
• Air Supply Weight: 11 lbs. (5 kg)
• Air Supply Material: Fire Retardant ABS/Stainless Steel
• Power Cord Length: 15 feet (457 cm)

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Product Specifications/Required Accessories
Material: Topside Material: nylon oxford
Underside Material: Teflon® impregnated polyester
Construction: RF-Welded
Width: 32” (81cm) or 39” (99 cm)
Length: 72” (183 cm)
Height: 30” (76 cm) Inflated (each chamber 7 1/2” [19 cm])
Required Accessory:
HoverTech International Air Supply
Part# HTAIR1200 (North American Version)
Part# HTAIR2300 (European Version)
All HoverTech International Products are Latex-Free.
For a full product listing go to www.HoverMatt.com.

Electromagnetic Compatibility Chart
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EMC: Table 1
Guidance and Manufacturer’s Declaration – Electromagnetic Emissions
The HoverTech International Air Supply is intended for use in the electromagnetic environment
specified below. The customer or the user of the HoverTech International Air Supply should ensure
that it is used in such an environment.
Emissions Test Compliance Electromagnetic Environment Guidance
RF emissions
CISPR11 Group 1
The HoverTech International Air Supply uses 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
CISPR11 Class A The HoverTech International Air Supply 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
For HTAIR-2300 ONLY

Electromagnetic Compatibility Chart
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For HTAIR-2300 ONLY
EMC: Table 2
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
The HoverTech International Air Supply is intended for use in the electromagnetic environment
specified below. The customer or the user of the HoverTech International Air Supply should ensure
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
± 6 kV contact
± 8 kV air
± 6 kV contact
± 8 kV air
Floors should be wood, concrete
or ceramic tile. If floors 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 supply
mains
± 1 kV for
input/output lines
Mains power quality should be
that of a typical commercial or
hospital environment.
Surge
IEC 61000-4-5
± 1 kV line(s) to
line(s)
± 2 kV line(s) to
earth
± 1 kV line(s) to
line(s)
± 2 kV line(s) to
earth
Mains power quality should be
that of a typical commercial or
hospital environment.
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
< 5% UT
(> 95% dip in UT)
For 0,5 cycle
40% UT
(60% dip in UT)
For 5 cycles
70% UT
(30% dip in UT)
For 25 cycles
< 5% UT
(>95% dip in UT) for
5 seconds
< 5% UT
(> 95% dip in UT)
For 0,5 cycle
40% UT
(60% dip in UT)
For 5 cycles
70% UT
(30% dip in UT)
For 25 cycles
< 5% UT
(>95% dip in UT) for
5 seconds
Mains power quality should be
that of a typical commercial or
hospital environment. If the user
of the HoverTech International Air
Supply requires continued
operation during mains
interruptions, it is recommended
that the HoverTech International
Air Supply be powered from an
uninterruptible power supply or a
battery.
Power Frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic fields
should be at levels characteristic
of a typical commercial or
hospital environment.
NOTE: U
T
is the AC mains voltage prior to application of the test level

Electromagnetic Compatibility Chart
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EMC: Table 3
Guidance and Manufacturer’s Declaration –Electromagnetic Immunity
The HoverTech International Air Supply is intended for use in the electromagnetic environment
specified below. The customer or the user of the HoverTech International Air Supply should ensure
that it is used in such an environment.
Immunity test IEC 60601
test level
Compliance
level Electromagnetic environment - guidance
Conducted RF IEC
61000-4-6
Radiated RF IEC
61000-4-3
3 Vrms
150 kHz to
80 MHz
3 V/m
80 MHz to
2.5 GHz
3 V
3 V/m
Portable and mobile RF communications equipment
should be used no closer to any part of the
HoverTech International Air Supply, including cables,
than the recommended separation distance
calculated from the equation applicable to the
frequency of the transmitter
Recommended separation distance
d= 1.2 √P
d=1.2 √P 80 to 800 MHz
d=2.3 √P 800 MHz to 2.5 GHz
Where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in meters (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site surveya,
should be less than the compliance level in each
frequency rangeb.
Interference may occur in the vicinity of equipment
marked with the following symbol:
NOTE 1: At 80 MHZ and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects, and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted
theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, and
electromagnetic site survey should be considered. If the measured field strength in the location in which the
device is used exceeds the applicable RF compliance level above, the device should be observed to verify
normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-
orienting or relocating the device.
b Over the frequency range 150 kHz to 80 MHz, the field strengths should be less than 3 V/m.
For HTAIR-2300 ONLY

Electromagnetic Compatibility Chart
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
EMC: Table 4

Recommended separation distances between portable and mobile RF
communications equipment and the HoverTech International Air Supply
The HoverTech International Air Supply is intended for use in an electromagnetic environment in
which radiated RF disturbances are controlled. The customer or the user of the HoverTech
International Air Supply can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and the
HoverTech International Air Supply as recommended below, according to the maximum output power
of the communications equipment.
Rated maximum
output power of
transmitter
W
Separation distance according to frequency of transmitter
m
15 kHz to 80 MHz
d=[3.5/V1]√P
80 MHz to 800 MHz
d=[3.5/V1]√P
800 MHz to 2.5 GHz
d=[7/E1]√P
0.01 0.12 0.12 0.23
0.10 .38 .38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation
distance d in meters (m) can be estimated using the equation applicable to the frequency of the
transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects, and people.

For HTAIR-2300 ONLY

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Cleaning & Maintenance
HoverJack® Air Patient Lift Cleaning Instructions
The HoverJack® air patient lift is constructed of nylon oxford. The HoverJack® air patient lift
may be covered with a sheet or other protective piece to help keep it clean. The HoverJack®
air patient lift can be wiped down with phenolic disinfectants, quaternaries, or other similar
type solutions as per hospital protocol for stretchers, or pads and/or bed mattresses.
Note: If using a protective sheet while moving a patient, make sure it doesn’t get caught
under the HoverJack® air patient lift. This could be a potential hazard.
*The HoverJack® air patient lift should not be laundered.
HoverJack® Air Patient Lift Maintenance Instructions
The HoverJack® air patient lift should be periodically inspected to ensure the following:
•Alldeflationvalvesareequippedwitharedcap.
•Theredcapsareintact.
•AllpatientsafetystrapsareattachedtotheHoverJack®airpatientlift.
•Allbucklesareintactandoperational.
•PullhandlesareallattachedtotheHoverJack®airpatientlift.
•Inflationvalvesareallself-sealingwithnoevidentleakage.
•TherearenopuncturesortearsintheHoverJack®airpatientlift.
Air Supply Cleaning and Maintenance
The air supply has an air filter on either side of the motor. These filters can be accessed by
removing the small screws holding the filter cover in place. Filters should be cleaned by hold-
ing under warn running water. Allow to air dry. As preventive maintenance, filter cleaning
should be performed monthly.
The Air Supply can be cleaned by wiping down using a damp cloth with soap and water or
mild neutral detergent. Dry using a clean, dry cloth or disposable paper towels.
*Do not spray cleaners or liquids directly on the air supply.
NOTE: CHECK YOUR LOCAL/STATE/FEDERAL/INTERNATIONAL GUIDELINES BE-
FORE DISPOSAL.

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Frequently Asked Questions
1. Can you over inflate the HoverJack® air patient lift and cause it to burst?
No, not if you are using the HoverTech International Air Supply. The HoverJack® air
patient lift has been tested under conditions that would “over-inflate” using this air supply.
2. If you open the red-capped valves, does the HoverJack® air patient lift deflate very
quickly, causing it to be unstable and the patient to fall?
Yes, if you open the red-capped valves all at one time. However, opening the redcapped
valves one at a time, beginning at the top chamber, permits the HoverJack® air patient
lift to deflate rather slowly, but steadily. The HoverJack® air patient lift remains stable
when deflated properly.
3. If we want the HoverJack® air patient lift to lift the patient a moderate amount, do all of
the chambers have to be inflated for it to be stable?
No. The HoverJack® air patient lift is made to be stable regardless of how many
chambers are inflated. However, the chambers MUST be inflated consecutively from the
floor up. In other words, if you only want to inflate 3 chambers, you must inflate
chambers 1, 2 & 3.
4. Will the HoverJack® air patient lift raise a very heavy patient?
Yes. The HoverJack® air patient lift has been successfully tested under the weight of 1900
pounds / 862 kg. When lifting heavy patients, extra caution must be taken to center them
properly on the HoverJack® air patient lift.

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AIR SUPPLY
NO USER SERVICEABLE PARTS.
Only qualified service personnel shall perform repairs on the HoverTech
International Air Supply.

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Part Identification
Handle /
Attachment Hook
Dust Cover
Hose Attachment Snap
Air Filter
Air Filter Cover
Hose
Bumpers Power Cord
(US/UK/Euro)
Power Cord
Strap
Foot
Information Labels
Power Cord Clamp
Grounding Pin
Used for a Ground Continuity (Bond) Test.
Circuit Breakers
Metal Cover
Control Panel
Label

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Power Cord / Clamp Replacement

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Handle Replacement
1. Remove the damaged handle by unscrewing the socket head screw from the barrel
nut using two 5/32” allen wrenches as shown.
2. Attach the new handle by reversing the process. When tightening the screw be sure
that the handle can rotate easily. The screw is treated with thread lock to secure it in
place.
Carrying Handle/
Attachment Hook
5/32” Allen
Wrench
5/32” Allen
Wrench
Socket
Head Screw
Barrel Nut