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SPIROHOME
®
FDA DOSSIER
Document No
SUS-FDAD
Publication Date
24.02.2019
USER MANUAL - PERSONAL
SPIROHOME
®
Revision Number
00
Revision Date
--
Page
3 / 44
1.Preface
1.1 Spirohome
®
Personal user manual version history
Version Number
Publication Date
Description
Rev.00
24.02.2019
Initial version for market launch
This revision of the Spirohome
®
Personal user manual applies to Spirohome
®
Personal devices
with a serial number between
S011900001-S011900150
.
Version histories of all Spirohome
®
user manuals can be found on the Spirohome
®
website
For any queries relating to the revision history of the user manual or product, please contact
your Spirohome
®
dealer or manufacturer.
1.2 Intended use of the Spirohome
®
Personal
The Spirohome
®
Personal is a prescription device for diagnostic spirometry testing of adult and
pediatric patients over the age of 5 who have been diagnosed with a chronic pulmonary disease
including, but not limited to, asthma, chronic obstructive pulmonary disease and cystic fibrosis.
It
is to be operated in the home setting by competent adult patients or caregivers of
patients.
1.3 About this user manual
This user manual should be read by users of the device prior to operating the Spirohome
®
Personal. Store this user manual in a clean and easily accessible place for future reference.
1.4 Legal Information
Contents of the user manual may be subject to change. Please refer to the Spirohome
®
website
for the latest version of user manuals. No part of this manual may be reproduced without the
written permission from Inofab.
© İnofab Sağlık Teknolojileri A.Ş, Ankara, Turkey. All rights reserved.
Spirohome
®
is a registered trademarks of İnofab Sağlık Teknolojileri A.Ş.
Spiroway
®
s a registered trademarks of İnofab Sağlık Teknolojileri A.Ş.
Bluetooth
®
is a registered trademark of Bluetooth SIG, Inc.
1.5 Electromagnetic Compatibility
Spirohome
®
Personal User Manual Rev.00 Feb 2019 İnofab Sağlık Teknolojileri A.Ş.
ODTÜ Teknokent / Silikon Blok K:1 No:15-A Çankaya / Ankara / Turkiye
.io
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