HOVERTECH HT-Air 2300 Air Supply User Manual
- June 9, 2024
- HOVERTECH
Table of Contents
- Symbol Reference
- Intended Use and Precautions
- Part Identification
- Air Supply Keypad Functions
- Product Specifications
- OPERATING CONDITIONS
- Cleaning
- PREVENTIVE MAINTENANCE
- INFECTION CONTROL
- Electromagnetic Compatibility Chart
- Returns and Repairs
- References
- Read User Manual Online (PDF format)
- Download This Manual (PDF format)
HT-Air® 2300
Air Supply
User Manual
Symbol Reference
**** | CE MARKING OF CONFORMITY |
---|---|
CAUTION | |
**** | OPERATING INSTRUCTIONS |
**MD** |
MEDICAL DEVICE |
HUMIDITY LIMITATION | |
AUTHORIZED REPRESENTATIVE | |
**SN** |
SERIAL NUMBER |
IMPORTER | |
**** | TYPE BF APPLIED PART |
**** | ALTERNATING CURRENT |
LATEX FREE | |
SINGLE PATIENT – MULTIPLE USE | |
**** | ELECTRICAL AND ELECTRONIC EQUIPMENT |
**UDI** |
UNIQUE DEVICE IDENTIFIER |
**** | KEEP DRY |
TEMPERATURE LIMITATION | |
MANUFACTURER | |
**LOT** |
LOT NUMBER |
**** | DATE OF MANUFACTURE |
**** | PROTECTIVE EARTH |
THIS END UP |
Intended Use and Precautions
The HT-Air® 2300 Air Supply provides six airflow options to inflate HoverTech’s air-assisted transfer, lift, and positioning devices. The Air Supply is used along with HoverTech’s air assisted devices to assist caregivers with patient transfers, positioning, turning and proning.
INTENDED CARE SETTINGS
Hospitals, long-term or extended care facilities
INTENDED USERS
- The caregiver/operator is the person handling the equipment.
- The patient is not the intended operator.
PRECAUTIONS
- 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.
- 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.
- When using the air supply in the MRI environment, a 25-ft. specialty MRI hose is required (available for purchase).
- Avoid electric shock. Do not open air supply.
- Reference product specific user manuals for operating instructions.
- Warning: To avoid the risk of electric shock, this equipment must only be connected to a supply main with protective earth.
- Warning: The HT-Air is not compatible with DC power supplies.
- Warning: The HT-Air is not intended for use with the HoverJack Battery Cart.
- Route the power cord in a manner to ensure freedom from hazard.
- Avoid blocking the air intakes of the air supply.
- Not for use in the presence of flammable anesthetics or in a hyperbaric chamber or oxygen tent.
Part Identification
CAUTION:
NO USER SERVICEABLE PARTS.
Only qualified service personnel shall perform repairs on the HoverTech
International Air Supply.
Air Supply Keypad Functions
ADJUSTABLE: For use with HoverTech air-assisted positioning devices. There are
four different 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).
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. The ADJUSTABLE
setting is a safety feature that can be used to ensure the patient is centered
on HoverTech air-assisted devices and to gradually accustom a patient who is
timid or in pain to both the sound and functionality of the inflated devices.
STANDBY: Used to stop inflation/air flow (Amber LED indicates STANDBY mode).
HOVERMATT 28/34: For use with 28″ & 34″ HoverMatts and HoverSlings.
HOVERMATT 39/50 & HOVERJACK: For use with 39″ & 50″ HoverMatts and HoverSlings
and 32″ & 39″ HoverJacks.
Product Specifications
Dimensions: | 12.5 x 7 x 7 inches (31.75 x 17.8 x 17.8 cm) |
---|---|
Weight: | 12.5 lbs (5.67 kg) |
Enclosure Material: | ABS rated UL94V-0/Stainless Steel |
Power Cord Set Length: | VDE Certified 15 feet (457 cm) |
Cord Type & Rating: | C13 90° Left, 10A, 250Vac |
Service Life: | 5 years |
Power Input: | 230Vac, 50 Hz, 6A (European version) |
Model #: HTAIR2300 (European Version) – 230Vac, 50Hz, 6A
CLASSIFICATION
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.
OPERATING CONDITIONS
Use Temperature: | 50° to 104° F (10° to 40° C) |
---|---|
Use Humidity: | 10% to 70% Non-Condensing |
Use Altitude: | 6,562ft / 2,000m |
Maximum Operation
Atmospheric Pressure Range:| 700 to 1,060 hPa
STORAGE AND TRANSPORT CONDITIONS
Storage/Shipping Temperature: | -40° to 158° F (-40° to 70° C) |
---|---|
Storage/Shipping Humidity: | 10% to 70% Non-Condensing |
CIRCUIT BREAKER
Max Operating Voltage: | 32Vdc; 250Vac, 50/60Hz |
---|---|
Current: | 6A |
Operating speed: | 5 to 30 seconds |
Size: | (0.54-0.55) inch x (0.625-0.635) inch |
Resettable Overload Capacity: | 10×12=120(A) |
Cleaning
Between patient use, clean and disinfect the surface of the air supply by
wiping it down with EPA approved hospital-grade disinfectant wipes or
disinfectant cleaner sprayed on a cleaning cloth. Follow disinfectant
manufacturer’s directions for dwell time and other instructions for use. Using
the disinfectant wipes/spray cleaner may degrade the graphics on the control
panel over time. Replacement panels can be purchased directly from HoverTech
International, if necessary.
NOTE: DO NOT SPRAY CLEANERS/LIQUIDS DIRECTLY ON THE AIR SUPPLY.
PREVENTIVE MAINTENANCE
Prior to use, a visual inspection should be performed on the air supply to
ensure the power cord is not frayed or nicked and that there is no visual
damage that would render the air supply unusable.
If any damage is found that would cause the air supply not to function as
intended, the air supply should be removed from use and returned to HoverTech
International for repair.
The air supply has air filters on either side of the motor. These filters can
be accessed by removing the small screws holding the filter covers in place.
It is recommended that the air filter is assessed per your facility’s
preventive maintenance schedule or annually. Filter should be cleaned if
clogged.
Remove the filter from the air supply and hold it under warm running water.
Allow the air filters to dry prior to placing back in the air supply. The
filter should be replaced when it is clogged with debris that does not break
free when it is washed. The filter should also be replaced if it begins to
lose its shape or deteriorate.
NOTE: IF AIR SUPPLY NEEDS TO BE DISPOSED, CHECK YOUR LOCAL / STATE / FEDERAL /
INTERNATIONAL GUIDELINES BEFORE DISPOSAL.
INFECTION CONTROL
When a HoverTech air supply is used in a patient room where isolation
protocols are being observed, the hospital should employ the same protocols/
procedures it utilizes for other equipment used in that patient room.
Between use with an airborne isolation patient, the air supply filters can be
removed and disinfected or replaced if hospital protocol requires. If the air
filters are disinfected, allow them to dry prior to placing back in the air
supply.
An air hose cover is available. These covers are disposable and come in a box
of 25 (Model #ASHC).
Electromagnetic Compatibility Chart
Guidance and manufacturer’s declaration – electromagnetic emissions
The HTAIR2300 is intended for use in the electromagnetic environment specified
below.
The customer or the user of the HTAIR2300 should assure that it is used in
such an environment.
Emission test | Compliance | Electromagnetic environment-guidance |
---|
RF emissions
CISPR 11| Group 1| The HTAIR2300 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
CISPR 11| Class A| The HTAIR2300 is suitable for use in all establishments,
including domestic establishments 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| Compliance
Guidance and manufacturer’s declaration – electromagnetic immunity
The HTAIR2300 is intended for use in the electromagnetic environment specified
below.
The customer or the user of the HTAIR2300 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| ± 6 kV contact ± 8 kV air| ± 6 kV
contact ± 8 kV air| Floors should be wood, concrete orceramic tile. If floors
are covered with
synthetic material, the relative humidity should be at least 30%
Electrical fast transient/ burst IEC 61000-4-4| ± 2kV for power supply lines ±
lkV for input/output lines| ± 2kV for power supply lines Not applicable| Mains
power quality should be that of a typical commercial or hospital environment.
Surge IEC 61000-4-5| ± 1kV line(s) to line(s) ± 2kV line(s) to earth| ± 1 kV
differential mode Not applicable| 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 s| <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 s| Mains power quality should be that of a
typical commercial or hospital environment.
Power frequency (50, 60 Hz) magnetic field IEC 61000-4-8| 3 A/m| 3 A/m| The
HTAIR2300 power frequency magnetic fields should be at levels characteristic
of a typical location in a typical commercial or hospital environment.
NOTE: UT is the a.c. mains voltage prior to application of the test level.
Electromagnetic Compatibility Chart
Guidance and manufacturer’s declaration – electromagnetic immunity
The HTAIR2300 is intended for use in the electromagnetic environment specified
below.
The customer or the user of the HTAIR2300 should assure 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 Vrms
3 V/m| Portable and mobile RF communications equipment should be used no
closer to any part of the HTAIR2300 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 MHz 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 metres (m). Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey, a should be less than the
compliance level in each frequency range.
Interference may occur in the vicinity of equipment marked with the following
symbol:
NOTE1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE2: 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, an electromagnetic
site survey should be considered. If the measured field strength in the
location in which the HTAIR2300 is used exceeds the applicable RF compliance
level above, the HTAIR2300 should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be necessary, such
as re-orienting or relocating the HTAIR2300.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less
than 3 V/m.
Electromagnetic Compatibility Chart
Recommended separation distance between portable and mobile RF communications
equipment and the HTAIR2300
The HTAIR2300 is intended for use in an electromagnetic environment in which
radiated RF disturbances are controlled. The customer or the user of the
HTAIR2300 can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment
(transmitters) and the HTAIR2300 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
---|---
150 kHz to 80 MHz
d =1,2VP| 80 MHz to 800 MHz
d =1,2VP| 800 MHz to 2,5 GHz
d =2,33/P
0,01| 0,12| 0,12| 0,23
0,1| 0,38| 0,38| 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 metres (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.
NOTE1: At 80 MHz and 800 MHz, the separation distance for the higher
frequency range applies.
NOTE2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures, objects
and people.
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
Attn: RGA #__
4482 Innovation Way
Allentown, PA 18109
For European companies, send returned products to:
Attn: RGA #____
Kista Science Tower
SE-164 51 Kista, Sweden
HoverTech International
4482 Innovation Way
Allentown, PA 18109
www.HoverMatt.com
Info@HoverMatt.com
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.
HT-Air2300Manual Rev. H
www.HoverMatt.com