Hovertech Q2 ROLLER User manual

TABLE OF CONTENTS
Intended Use and Precautions........................................2
Part Identification - Q2Roller...........................................2
Part Identification - Air Supply........................................2
Air Supply Keypad Functions..........................................3
Instructions for Use ........................................................3
Product Specifications/Required Accessories..................3
Cleaning & Maintenance ...............................................4
Returns and Repairs........................................................4
Lateral Turning Device
User Manual
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User Manual
2| HoverTech International Q2RollerManual Rev. G
Intended Use and Precautions
INDICATIONS FOR USE
Patients who are unable to turn or laterally position themselves
CONTRAINDICATIONS
Patients who are experiencing thoracic, cervical or lumbar fractures that are
deemed unstable
INTENDED CARE SETTINGS
Hospitals, long-term or extended care facilities
PRECAUTIONS
• Ensure the Q2Roller meets the patient’s needs before using.
• Always use a minimum of two caregivers when operating the Q2Roller.
• Ensure valves are not in contact with the patient while on the Q2Roller.
• Product should only be used by trained personnel.
• Only use attachments and/or accessories that are authorized by
HoverTech International.
• Use of this device with products or accessories not authorized
by HoverTech International could result in injury or equipment
malfunction and may void the Manufacturer’s Warranty. HoverTech
International will not be held responsible for any injuries or damages
caused due to the improper use of this device.
• Use the Q2Roller according to instructions.
• Only for use with the HT-Air air supply adjustable button.
• Make sure patient is centered on the Q2Roller before inflating.
Reference Center Line Indicator on the Q2Roller.
• Caregivers must ensure patient is attended and stabilized during
Q2Roller inflation, deflation or when inflated at angles greater than
30 degrees.
• Do not launder.
• Reference product-specific user manuals for additional operating
instructions.
PRECAUTIONS – HOVERTECH INTERNATIONAL
AIR SUPPLY
• Route the power cord in a manner to ensure freedom from hazard.
• Avoid blocking the air intakes of the air supply.
• Use this product only for its intended purpose as described in this
manual.
• CAUTION: Avoid electric shock. Do not open air supply.
Part Identification - Q2Roller
Center Line Indicator
Black Inflation Valve (2)
Red Deflation Valve (2)
Turning Chambers
Securing Apron
Air Filter
Cover
Hose
Nozzle
Hose
Hose Release Button
Control Panel Label
Carrying Handle/
Attachment Hook
Power
Cord
Strap
Power
Cord
WARNING: The HT-Air is not compatible with DC power supplies.
The HT-Air is not intended for use with the HoverJack Battery Cart.
CAUTION: NO USER SERVICEABLE PARTS.
Only qualified service personnel shall perform repairs on the
HoverTech International Air Supply.
Part Identification - Air Supply

User Manual
Q2RollerManual Rev. G www.HoverMatt.com | 3
Air Supply Keypad Functions
Transfer
Speed
High
Adjustable/
Pressure
Setting
Transfer
Speed
Low
Standby (Amber LED)
Power IndicationAdjustable Speed
Indication
(Green Flashing LED)
Green LEDs
The ADJUSTABLE keypad function has four dierent settings.
Each press of the button increases the air pressure and rate
of inflation. The Green Flashing LED will indicate the inflation
speed by the number of flashes (i.e. two flashes equals the
second inflation speed).
STANDBY: Used to stop inflation/air flow (Amber LED indicates
STANDBY mode).
Instructions for Use
1. Ensure the red deflation valves are capped tightly before beginning
inflation.
2. Place the Q2Roller on the bed mattress, and center using the Center
Line Indictor.
3. Tuck the securing apron of the Q2Roller under the bed mattress to
keep it in place during use.
4. Remove the backing from the adhesive strips on the Q2R Pad, and
center it on top of the Q2Roller (if the patient is already on the
mattress, place the device and pad under the patient using a
log-rolling technique).
5. With the patient centered on the device, ensure all bed/stretcher
rails are up, or follow your facility’s protocol.
6. Locate the inflation valve on the OPPOSITE side of the turn direction,
and place the air supply hose over the valve. Press the ADJUSTABLE
button on the HT-Air keypad to initiate air flow. If necessary, press this
button up to 3 more times to increase air flow and rate of inflation.
7. When the turn is complete, remove the hose from the valve and press
the STANDBY button on the air supply keypad to stop air flow. Cham-
ber may not need to be fully inflated to achieve desired position.
8. To quickly deflate the Q2Roller, remove the red cap from the deflation
valve. To slowly deflate or adjust the chamber, depress the center of
the black inflation valve.
Product Specifications/Required Accessories
Q2ROLLER®LATERAL TURNING DEVICE
Material: Polyurethane
Construction: RF Welded
Width:
Chambers: 46.5" (118 cm)
(combined chamber width)
Apron: 72" (183cm)
Length: Chambers: 44.5" (113 cm)
Apron: 44" (112 cm)
LATEX FREE
Model #: HTR-200
Patient Weight Limit: 600 lbs. (272 kg)
Single-Patient Use
Q2R®PAD
Material: Non-Woven, Breathable PE
Construction: Thermal Bonding
Width: 39” (99 cm)
Length: 39” (99 cm)
Model #: HTR-CHX-5PACK (5 ea.)
Model #: HTR-CHX-CASE (50 ea.)
REQUIRED ACCESSORY:
Model #: HTAIR1200 (North American Version) – 120V~, 60 Hz, 10A
Model #: HTAIR2300 (European Version) – 230V~, 50 Hz, 6A
Model #: HTAIR1000 (Japanese Version) – 100V~, 50/60 Hz, 12.5A
Model #: HTAIR2356 (Korean Version) – 230V~, 50/60 Hz, 6A

User Manual
4| HoverTech International Q2RollerManual Rev. G
Cleaning & Maintenance
CLEANING
The Q2Roller is a single-patient use device. If the device becomes soiled,
completely wipe it down using a germicidal cleaner (phenolic disinfectant,
quaternary solution or other intermediate level disinfectant according to
facility procedure) to disinfect. For best results, follow the cleaner manufac-
turer’s recommended dwell time and instructions for use. Apply germicidal
cleaner directly into hard-to-reach areas. Let air dry. Do not launder.
INFECTION CONTROL
The Q2R Pad is recommended to cover the Q2Roller to keep the device from
getting soiled (also available for separate purchase). Other materials, such as
pads or linens, may also be placed on top of the Q2Roller to keep it clean.
If the Q2Roller is used on an isolation patient, the hospital should employ
the same protocols/procedures it utilizes for the bed mattress and/or for
the linen in that patient room.
AIR SUPPLY CLEANING AND MAINTENANCE
See air supply manual for reference.
NOTE: CHECK YOUR LOCAL/STATE/FEDERAL/INTERNATIONAL GUIDELINES
BEFORE DISPOSAL.
PREVENTIVE MAINTENANCE
Prior to use, a visual inspection should be performed on the Q2Roller to
ensure that there is no visible damage that would render the Q2Roller
unusable.
The Q2Roller should be periodically inspected to ensure the following:
• All inflation valves are self-sealing with no evidence of leakage
• There are no punctures or tears in the Q2Roller
If any damage is found that would cause the Q2Roller not to function as
intended, the Q2Roller should be discarded.
4482 Innovation Way
Allentown, PA 18109
800.471.2776
Fax [phone]
www.HoverMatt.com
[e-mail]
Returns and Repairs
All products being returned to HoverTech International (HTI) must have a
Return Goods Authorization (RGA) number issued by the company. Please
call 800-471-2776 and ask for a member of the RGA Team, who will issue
you an RGA number. Any product returned without an RGA number will
cause a delay in the repair time.
Returned products should be sent to:
HoverTech International
4482 Innovation Way
Allentown, PA 18109
Attn: RGA #______________________
Phone: [phone]
Fax: [phone]
For European companies, send returned products to:
Attn: RGA #____________
Kista Science Tower
SE-164 51 Kista, Sweden
www.Etac.com
[e-mail]

HoverTech Symbols
ManualSymbols, Rev. A www.HoverMatt.com
Date Revised: 5/20/21
CE MARKING OF CONFORMITY
CAUTION
OPERATING INSTRUCTIONS
MEDICAL DEVICE
HUMIDITY LIMITATION
AUTHORIZED REPRESENTATIVE
SERIAL NUMBER
SINGLE PATIENT – MULTIPLE USE
ELECTRICAL AND ELECTRONIC EQUIPMENT
UNIQUE DEVICE IDENTIFIER
KEEP DRY
TEMPERATURE LIMITATION
MANUFACTURER
LOT NUMBER
HoverTech International
4482 Innovation Way
Allentown, PA 18109
www.HoverMatt.com
[email protected]
These products comply with
the standards applicable for
Class 1 products in the
Medical Device Regulation
(EU) 2017/745 on medical
devices.
CEpartner4U , ESDOORNLAAN 13,
3951DB MAARN, THE NETHERLANDS.
www.cepartner4u.com
In case an adverse event in relation to the
device, incidents should be reported to
our authorized representative,
CEPartner4u. CEPartner4u will forward
information to the manufacturer.