Cleaning And Maintenance; Specifications; Spare Parts And Accessories; Electromagnetic Compatibility - Maxtec UltraMax O2 Instructions For Use Manual

6.0 CLEANING AND MAINTENANCE
Use caution to prevent any fluid from entering the UltraMax O2.
DO NOT soak or immerse the UltraMax O2 in fluid.
DO NOT autoclave or expose the UltraMax O2 to ethylene oxide sterilization.
6.1 Cleaning
Wipe down the exterior surfaces of the UltraMax O2 with a moist cloth and mild hand or dish
soap (pH 6-8).
6.2 Maintenance
Replace the batteries with high quality AA Alkaline or Lithium batteries.
DO NOT use rechargeable batteries.
When not in use for periods greater than 30 days, remove the batteries to protect the
•
UltraMax O2 from potential battery leakage.
Store the UltraMax O2 between -15˚C and 60˚C (5˚F - 140˚F)
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7.0 SPECIFICATIONS
Oxygen
Oxygen Measurement Range
(from a concentrator) ......................................................................................................... 20.9 - 96%
Oxygen Measurement Accuracy .......................................................................±1.5 % of full scale at
Oxygen Measurement Resolution ..................................................................................0.1% Oxygen
Flow
Flow Measurement Range ................................................................................................... 0 - 10 LPM
Flow Measurement Accuracy ................................................................................................ ±0.2 LPM
Flow Measurement Resolution ................................................................................................0.1 LPM
Pressure
Pressure Measurement Range ............................................................0.5 - 50 (PSI), 3.4 - 344 (kPa)
Pressure Measurement Accuracy .............................................................. ±0.5% (PSI), ±0.5% (kPa)
Pressure Measurement Resolution .......................0.1 (PSI), 0.1 up to 199, 1 from 200 to 344 (kPa)
Response Time ................................................................................................................. ≤17 seconds
Warm-up Time .....................................................................................................................< 1 second
Operating Temperature ..............................................................................15˚C - 40˚C (59˚F-104˚F)
Storage Temperature ..................................................................................-15˚C - 60˚C (5˚F-140˚F)
Pressure ....................................................................................................................800 - 1000 mBars
Humidity ...................................................................................................0 - 95% (non-condensing)
Power Requirements ..............................................................2 AA Alkaline batteries (2 x 1.5 Volts)
Battery Life ...................................................................................≥ 1,100 hours (16,500 read cycles)
Low Battery Indication ........................................................... "Low Battery" icon displayed on LCD
Dimensions ....................................................3.16" x 5.10" x 1.04" (80.3mm x 129.5mm x 26.4mm)
Weight .............................................................................................................................0.4 lbs (181 g)
8.0 SPARE PARTS AND ACCESSORIES
8.1 Included with Your Unit
PART NUMBER
R211M11
RP46P05
8.2 Optional Accessories
PART NUMBER
R221P15
Repair of this equipment must be performed by a qualified service technician experienced in
repair of portable hand held medical equipment.
WWW.MAXTEC.COM • (800) 748-5355
constant temperature and optimal flow*
ITEM
Operating Manual and Instructions for Use*
Gas Sample Tubing
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Soft Cover
Equipment in need of repair shall be sent to:
Maxtec
Customer Service Department
2305 South 1070 West
Salt Lake City, UT 84119
(Include RMA number issued by Customer Service)
9.0 ELECTROMAGNETIC
COMPATIBILITY
The information contained in this section (such as separation distances) is in general spe-
cifically written with regard to the UltraMax O2. The numbers provided will not guarantee
faultless operation but should provide reasonable assurance of such. This information may
not be applicable to other medical electrical equipment; older equipment may be particularly
susceptible to interference.
Note: Medical electrical equipment requires special precautions regarding electromagnetic
compatibility (EMC) and needs to be installed and put into service according to the EMC infor-
mation provided in this document and the remainder of the instructions for use this device.
Portable and mobile RF communications equipment can affect medical electrical equipment.
Cables and accessories not specified within the instructions for use are not authorized. Using
other cables and/or accessories may adversely impact safety, performance and electromag-
netic compatibility (increased emission and decreased immunity).
Care should be taken if the equipment is used adjacent to or stacked with other equipment;
if adjacent or stacked use is inevitable, the equipment should be observed to verify normal
operation in the configuration in which it will be used.
ELECTROMAGNETIC EMISSIONS
This equipment is intended for use in the electromagnetic environment specified below.
The user of this equipment should assure that it is used in such an environment.
COMPLIANCE
EMISSIONS
ACCORDING TO
RF Emissions Group 1
(CISPR 11)
CISPR Emissions Class A
Classification
Harmonic Emissions Class A
(IEC 61000-3-2)
Voltage Fluctuations Complies
5
ELECTROMAGNETIC ENVIRONMENT
The UltraMax O2 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.
The UltraMax O2 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.
NOTE: The EMISSIONS characteristics of this
equipment make it suitable for use in industrial
areas and hospitals (CISPR 11 class A). If it is used
in a residential environment (for which CISPR
11 class B is normally required) this equipment
might not offer adequate protection to radio-
frequency communication services. The user
might need to take mitigation measures, such
as relocating or re-orienting the equipment.
ENGLISH