Classifications - Fisher & Paykel SleepStyle Auto Guía De Uso Y Cuidado

Outlet air temperature
Noise level
Water chamber volume
Standards compliance
Cellular modem
Bluetooth technology
FCC compliance
Data recording
Service life
General

8.4 CLASSIFICATIONS

Mode of operation
Electric shock protection
Ingress protection
Maximum = 38 °C (100 °F)
Sound pressure level 28 ±1.5 dBA; average sound power level <35 dBA.
380 mL up to the maximum water-level line
IEC 60601-1:2012; IEC 60601-1-2:2014; IEC 60601-1-2:2007; IEC 60601-1-11:2015;
ISO 80601-2-70:2015; ISO 5356-1:2004; ISO 17510-1:2007; ISO 8185:2007
UMTS 3G: Bands 1, 2, 5, 6, 8, 19
GSM 2G: 850 MHz/900 MHz/1800 MHz/1900 MHz
2402 – 2480 MHz
This device has been tested and found to comply with the limits for a Class B digital
device, pursuant to part 15 of the FCC Rules. These limits are designed to provide
reasonable protection against harmful interference in a residential installation. This
device generates, uses, and can radiate radio frequency energy and, if not installed
and used in accordance with the instructions, may cause harmful interference to
radio communications. However, there is no guarantee that interference will not
occur in a particular installation. If this device does cause harmful interference to
radio or television reception, which can be determined by turning the device off and
on, the user is encouraged to try to correct the interference by one or more of the
following measures:
• Reposition or relocate the receiving antenna.
• Increase the separation between the device and receiver.
• Connect the device into an outlet on a circuit different from that to which the
receiver is connected.
• Consult your healthcare provider or your Fisher & Paykel Healthcare
representative for help.
The InfoUSB will store up to 5 years of summary efficacy data, 365 days of detailed
efficacy data, and 140 hours of high-resolution pressure, leak and flow data. Without
an InfoUSB, the device's internal memory is capable of storing up to 1 year of
summary efficacy data, 30 days of detailed efficacy data, and 20 hours of high-
resolution pressure, leak, and flow data.
Device
Breathing tubes
Water chamber
Air filter
The patient is an intended operator.
Continuous operation
Type BF
IP22
5 years
12 months
12 months
3 months
ENGLISH A-21