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2010-8401CE-E
February 2018
Page 4 of 8
Humidifier - Figure 3
Cannula - Figure 4
Flow adjustment knob (Fig 1-1)
ABS
Cabinet air filter (Fig 2-9)
Polyester
Mains cable (Fig 2-8)
PVC
Inlet Filter (Fig 5)
Polypropylene
Humidifier
Polypropylene
Casters
Nylon
Pipe/Tubing
Aluminum, PVC,
polyurethane and/or
silicone
2.5
Accessories and Spare Parts
The accessories used with the
device
must be oxygen
compatible,
designed
for
oxygen
therapy
use,
biocompatible and comply with the general requirements
of the FDA Quality System Regulation or the 93/42/EEC
European Directive, or any other applicable regulatory
requirements.
The accessories below, available from
Nidek Medical
Products, Inc.
and our distributors, comply with these
requirements. Contact your equipment supplier to obtain
these accessories.
Accessories
Part Ref
Humidifier (1 to 5 LPM)
9012-8774
Cannula with 2m (7ft) tubing (1 to 5 LPM)
9012-8780
Extension Tubing 7.7m (25 ft)
9012-8781
Tubing Adapter
9012-8783
Petroleum and oil based lubricants, lotions and cosmetics
are flammable and the use of them while operating the
device is hazardous.
Improper patient connection to and use of the cannula
may result in injury, including strangulation. To reduce the
risk of this occurring, avoid situations that might cause the
cannula or hose to become entangled about the patient’s
neck and do not attach more than 15.5m (50 ft) in length
of tubing.
Ears, nose and neck may become irritated after prolonged
exposure to the cannula. For relief, only a water based
lubricant is recommended.
Nasal passages may become irritated after prolonged
exposure to the product gas. If this occurs, consult your
physician about using a humidifier during treatment.
The use of certain administration accessories and/or spare
parts which are not recommended by the manufacturer
may reduce its performance and void the manufacturer’s
responsibility.
Spare Parts
Part Ref
Cabinet air filter (Fig 2-9)
8400-1025
Inlet Filter (Under Fig 2-9)
8400-1180
Ventilation Grill (Fig 2-9)
8400-0108
Casters
8300-8068
Mains Cable Wrap
8400-0022
Please consult the Nuvo Lite Maintenance Manual (PN
2010-8405) for instructions on replacing any above spare
parts.
3
UNPACKING AND INSPECTION
The Oxygen Concentrator is packaged to protect the
device from damage while being transported and stored.
After the device is removed from the package, inspect
for damage. If damage is detected, please contact your
equipment provider.
If you do not plan to use your
device
immediately, please
consult the Environmental Storage Conditions below.
Environmental Storage Conditions:
The
device
should be stored in a dry area, with an
ambient temperature between -20°C to 60°C (0°F to
140°F) at 15-95% relative humidity. It must be stored,
transported and used in the vertical position only.
Oxygen concentration can be affected after prolonged
periods of storage – check device before use.
4
INSTALLATION AND OPERATION
4.1
Installation
Environmental Operating Conditions:
The device should be operated in a dry area, with an
ambient temperature between 10°C to 40°C (50°F to
105°F) at 15-95% relative humidity. The device can be
operated at an altitude of up to 2200m (7500ft) at a
temperature of 21°C (70°F) without causing product
degradation.
DO NOT use in explosive atmosphere.
To avoid risk of fire and explosion the concentrator should
be kept away from heat sources, incandescent sources,
solvents, Aerosols, etc.
Unit should be placed and operated in a well-ventilated
space that is free of pollutants or fumes and protected
from the elements with adequate lighting.
Unit should be placed and operated in a space where the
position and storage of the mains cable (Fig 2-8) and
oxygen tubing do not present a tripping hazard. The
mains cable should be easily accessible for disconnection.
For patient safety and benefit, no modification to the
equipment is allowed. It is also not recommended to
interconnect the device with any equipment or
accessories not specified in this guide.
