7. Specifications
EN
33
Notes:
• These specifications are subject to change without notice.
• In the clinical validation study, the 5th phase was used on 85 subjects for determination of diastolic blood
pressure.
• This device has not been validated for use on pregnant patients.
• IP classification is degrees of protection provided by IEC 60529.
• This device fulfils the provisions of EC directive 93/42/EEC (Medical Device Directive).
• This device is designed according to the European Standard EN1060, Non-invasive
sphygmomanometers Part 1: General Requirements and Part 3: Supplementary
requirements for electromechanical blood pressure measuring systems.
• This OMRON device is produced under the strict quality system of OMRON HEALTHCARE
Co., Ltd., Japan. The core component for OMRON devices, which is the Pressure Sensor, is
produced in Japan.
This Product operates in the unlicensed ISM band at 2.4GHz. In case this Product is used
around the other wireless devices including microwave and wireless LAN, which operate same
frequency band of this Product, there is a possibility that interference occurs between this
Product and such other devices. If such interference occurs, please stop the operation of other
devices or relocate this Product before using this Product or do not use this Product around the
other wireless devices.
The
Bluetooth
®
Smart
word mark and logos are registered trademarks owned by Bluetooth SIG,
Inc. and any use of such marks by OMRON HEALTHCARE Co., Ltd. is under license. Other
trademarks and trade names are those of their respective owners.
Apple and the Apple logo are trademarks of Apple Inc., registered in the U.S. and other countries.
App Store is a service mark of Apple Inc.
Android and Google Play are both trademarks of Google Inc.
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