F&P Airvo2 Manual Del Usuario página 18

PRODUCT SPECIFICATIONS
Dimensions
Weight
Supply frequency
Supply voltage/current
Sound pressure level
Auditory alarm pause
Expected service life
Serial port
Warm-up time
*
Flow rates are measured in BTPS (Body Temperature/Pressure, Saturated)
† Inrush current may reach 50A
OPERATING CONDITIONS
Ambient temperature
Humidity
Altitude
Mode of operation
WARNING
• Do not use the unit at an altitude above 2000 m (6000 ft) or outside a temperature range of 18 - 28 °C (64 - 82 °F).
Doing so may affect the quality of the therapy or injure the patient.
Designed to conform to the
requirements of:
IEC 60601-1:2005 + A1:2012
IEC 60601-1-2:2014
ANSI/AAMI 60601-1:2005/(R) 2012
CAN/CSA-C22.2 No. 60601-1:2014
EN 60601-1:2006 + A1:2013
ISO 80601-2-74:2017
Accessory equipment connected to the serial port of the device must be certified to either IEC 60601-1 or IEC 60950-1.
Furthermore all configurations shall comply with the system standard IEC 60601-1-1. Anyone who connects additional
equipment to the signal input part or signal output part configures a medical system and is therefore responsible for
ensuring that the system complies with the requirements of the system standard IEC 60601-1-1. If in doubt, consult the
technical services department or your local representative.
DISPOSAL INSTRUCTIONS
Unit Disposal Instructions
This unit contains electronics. Please do not discard with regular waste. Return to Fisher & Paykel
Healthcare or dispose according to local guidelines for disposing of electronics. Dispose according to Waste
Electrical and Electronic Equipment (WEEE) directive in European Union.
Consumables Disposal Instructions
Place the interface, breathing tube and chamber in a waste bag at the end of use. Hospitals should discard
according to their standard method for disposing of contaminated product.
295 mm x 170 mm x 175 mm
(11.6" x 6.7" x 6.9")
2.2 kg (4.8 lb) unit only,
3.4 kg (7.5 lb) packaged in bag
incl. accessories
50-60 Hz
100-115 V 2.2 A (2.4 A max†)
220-240 V 1.8 A (2.0 A max†)
Alarms exceed 45dbA @ 1 m
115 seconds
5 years
The serial port is used for
downloading product data,
using F&P Infosmart™ software.
10 minutes to 31 °C (88 °F),
30 minutes to 37 °C (98.6 °F)
using a MR290 chamber with
flow rate of 35 L/min and
starting temperature 23 ± 2 °C
(73 ± 3 °F)
18 - 28 °C (64 - 82 °F)
10 - 95% RH
0 - 2000 m (6000 ft)
Continuous operation
The unit complies with the electromagnetic compatibility requirements of
IEC 60601-1-2. In certain circumstances, the unit may affect or be affected by
nearby equipment due to the effects of electromagnetic interference. Excessive
electromagnetic interference may affect the therapy delivered by the unit.
If this should happen, try moving the unit or the location of the unit causing
interference, or alternatively consult your healthcare provider. To avoid potential
interference, do not place any part of the device or accessories within 30 cm
(12") of any portable or mobile radio frequency communication equipment.
Target temperature
settings
Humidity performance
Maximum temperature
of delivered gas
Maximum surface
temperature of applied
parts
Flow range (default)
Flow range
(Junior Mode)
Maximum oxygen input 60 L/min
Oxygen analyzer
accuracy
STORAGE AND TRANSPORT CONDITIONS
AIRVO
Ambient temperature
Humidity
Tube & chamber kits
Ambient temperature
Humidity
The unit may require up to 24 hours to warm up or cool down
from the minimum or maximum storage temperature before it is
ready for use.
A – 14
37, 34, 31 °C
>33 mg/L at 37 °C target
>12 mg/L at 34 °C target
>12 mg/L at 31 °C target
43 °C (109 °F)
(in accordance with ISO 80601-2-74)
44 °C (111 °F)
(in accordance with ISO 80601-2-74)
10-60 L/min*
2-25 L/min*
< ± 4 %
(within the range 25-95% O
Operating conditions:
18-28 °C (64-82 °F),
30-70% RH
-10 - 60 °C (14 - 140 °F)
10 - 95% RH, non-condensing
-10 - 50 °C (14 - 122 °F)
10 - 95% RH, non-condensing
)
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