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ResMed Ltd 2016.
DOC NO 378015
PAGE 2 of 35
– PRINTED MATERIALS
REV 5
REVISION 5
Changes trigger new document numbers for published multis if published multis are already available
Section Heading Summary of change
Languages/Country variations
Update of AMER SPA/POB exception:
Technical specifications: Remove
FCC ID: 2ACHL-AIR104G, 2ACHL-AIR103G
IC: 9103A-AIR104G, 9103A-AIR103G
The AirCurve 10 device complies with FCC Rules and Industry Canada
rules.
The AirCurve 10 device should be used at a minimum distance of 0.8" (2
cm) from the body during operation.
Additional information regarding the FCC Rules and IC compliance for this
device can be found on www.resmed.com/downloads/devices
Therapy data
Update paragraph to include ‘if wireless network is available’
Wireless – Notes section
Add a new paragraph under the bullet points:
Please be aware that within the wireless network the availability and
quality of the network may be affected by terrain, buildings and the
weather. Wireless communication depends on network availability.
Coverage is not available everywhere and varies by service.
Technical Specifications
classification
Update classification table to: IEC 60601-1:2005+A1:2012
Technical Specifications – wireless
module
Update the technology section with the following:
4G (USA and Canada only)
3G (USA and Canada only)
2G GSM (all regions except USA and Canada)
Technical Specifications – FCC
rules
Update with the following:
FCCID: 2ACHL-AIR104G, 2ACHL-AIR103G
IC: 9103A-AIR104G, 9103A-AIR103G
The AirCurve 10 device complies with FCC Rules and Industry Canada
Rules
REVISION 4
Backwards compatible change / Changes trigger new document numbers for published multis
Section Heading Summary of change
All Technical review: >378013-8#1
Data according to D000-0245 Machines Data Rev. 55
Caring for your device The following Legionella warning added after the first paragraph:
“Regularly clean your tubing assembly, water tub and mask to receive optimal
therapy and to prevent the growth of germs that can adversely affect your
health”.
The following LMR 880 was added to the list of warnings:
“Regularly check the antibacterial filter for signs of moisture or other
contaminants, particularly during nebulization or humidification. Failure to do so
could result in increased breathing system resistance.”
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