Technical Information - F&P Airvo 2 PT101 Serie Manual Del Usuario

5. TECHNICAL INFORMATION

SYMBOL DEFINITIONS
Caution Type BF ATTENTION
Hot Surfaces Applied Part Consult
accompanying
documents
PRODUCT SPECIFICATIONS
295 mm x 170 mm x 175 mm
Dimensions
(11.6" x 6.7" x 6.9")
2.2 kg (4.8 lb) unit only,
Weight 3.4 kg (7.5 lb) packaged in bag
incl. accessories
Supply frequency 50-60 Hz
100-115 V 2.2 A (2.4 A max)
Supply voltage/current
220-240 V 1.8 A (2.0 A max)
Sound pressure level Alarms exceed 45dbA @ 1 m
Auditory alarm pause 115 seconds
The serial port is used for
Serial port 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
Warm-up time
flow rate of 35 L/min and
starting temperature 23 ± 2 °C
(73 ± 3 °F)
Designed to conform to the requirements of:
IEC 60601-1
UL 60601-1 The unit complies with the electromagnetic compatibility requirements of IEC 60601-1-2. In
CSA C22.2/No. 601.1 certain circumstances, the unit may affect or be affected by nearby equipment due to the
AS 3200.1.0 effects of electromagnetic interference. If this should happen, try moving the unit or the
EN 60601-1 location of the unit causing interference, or alternatively consult your healthcare provider.
ISO 8185
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.
OPERATING CONDITIONS
Ambient temperature
Humidity
Altitude
Mode of operation
STORAGE AND TRANSPORT CONDITIONS
The unit should be stored and transported in environmental conditions of -10 °C to 60 °C (14 °F to 140 °F),
10 to 95% RH, non-condensing.
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.
Do not Drip Proof Alternating
throw away Current
Target temperature
settings
Humidity
Maximum temperature
of delivered gas
Flow range (default)
Flow range
(Junior Mode)
Maximum oxygen input 60 L/min
Oxygen analyzer
accuracy
18 - 28 °C (64 - 82 °F)
10 - 95% RH
0 - 2000 m (6000 ft)
Continuous operation
A – 13
Class ll Power 93/42/EEC
Double
On/Off Class IIa
Insulated
(Standby)
37, 34, 31 °C
>33 mg/L at 37 °C target
>10 mg/L at 34 °C target
>10 mg/L at 31 °C target
43 °C (109 °F)
(in accordance with ISO 8185:2007)
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
)
2