iHealth BP3 Bedieningshandleiding - Pagina 3
Blader online of download pdf Bedieningshandleiding voor {categorie_naam} iHealth BP3. iHealth BP3 11 pagina's. Fully automatic arm cuff electronic blood pressure dock
Ook voor iHealth BP3: Gebruikershandleiding (12 pagina's), Snelstarthandleiding (2 pagina's)
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The Blood Pressure Dock is for use with iPod touch
, iPhone
or iPad
.
The iHealth Blood Pressure Dock is made for the following models:
iPod touch 4th generation
iPod touch 3rd generation
iPod touch 2nd generation
iPhone 4S
iPhone 4
iPhone 3GS
iPhone 3G
iPhone
iPad 2
iPad
iHealth is a trademark of iHealth Lab Inc.
"Made for iPod", "Made for iPhone", and "Made for iPad" mean that an electronic
accessory has been designed to connect specifically to iPod, iPhone, or iPad,
respectively, and has been certified by the developer to meet Apple performance
standards. Apple is not responsible for the operation of this device or its
compliance with safety and regulatory standards. Please note that the use of this
accessory with iPod, iPhone, or iPad may affect wireless performance. iPad,iPhone,
and iPod Touch are trademarks of Apple Inc.,registered in the U.S. and other
countries.
CONTRAINDICATION
It is inappropriate for people with serious arrhythmia to use this Electronic
Sphygmomanometer.
PRODUCT DESCRIPTION
Based on Oscillometric methodology and silicon integrated pressure sensor, blood
pressure and pulse rate can be measured automatically and non-invasively. The
measurement results include blood pressure and pulse rate will displayed on iPod
touch, iPhone, or iPad and can be stored in the memory with date and time stamp.
The Electronic Sphygmomanometer corresponds to the below standards: IEC
60601-1:1988 A1:1991+A2:1995(Medical electrical equipment-Part1:General
requirements for safety) ,IEC 60601-1-2 2007(Medical electrical equipment-
Part1:General requirements for safety; Collateral Standard-Electromagnetic
compatibility-Requirements and tests) ,EN 1060-1: 1995 + A1: 2002 + A2: 2009
(Non-invasive sphygmomanometers - Part 1: General requirements), EN 1060-3:
1997 + A1: 2005 + A2: 2009 (Non-invasive sphygmomanometers - Part 3:
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