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8
EN
Note
• These specifications are subject to change without notice.
• This monitor is clinically investigated according to the requirements of ISO 81060-2:2013. In the clinical validation study, K5 was used on 85
subjects for determination of diastolic blood pressure.
• IP classification is degrees of protection provided by enclosures in accordance with IEC 60529. This monitor and optional AC adapter are
protected against solid foreign objects of 12.5 mm diameter and greater such as a finger. The optional AC adapter is protected against vertically
falling water drops which may cause issues during a normal operation.
About a wireless communication interference
This product operates in an unlicensed ISM band at 2.4 GHz. In the event this Product is used near other wireless devices such as microwave and
wireless LAN, which operate on the same frequency band as this Product, there is a possibility that interference may occur. If interference occurs,
stop the operation of the other devices or relocate this Product away from other wireless devices before attempting to use it.
6. Correct Disposal of This Product (Waste Electrical & Electronic Equipment)
This marking shown on the product or its literature, indicates that it should not be disposed of, with other household wastes at the end of its
working life.
To prevent possible harm to the environment or human health from uncontrolled waste disposal, please separate this product from
other types of wastes and recycle it responsibly to promote the sustainable reuse of material resources.
Household users should contact either the retailer where they purchased this product, or their local government office, for details of
where and how they can return this item for environmentally safe recycling.
Business users should contact their supplier and check the terms and conditions of the purchase contract. This product should not be mixed with
other commercial waste for disposal.
Disposal of used batteries should be carried out in accordance with local regulations.
7. Important Information Regarding Electromagnetic Compatibility (EMC)
HEM-7157T manufactured by OMRON HEALTHCARE Co., Ltd. conforms to EN 60601-1-2:2015 Electromagnetic Compatibility (EMC) standard.
Further documentation in accordance with this EMC standard is available at:
Asia Pacific: https://www.omronhealthcare-ap.com/emc-information
Taiwan: https://www.omronhealthcare.com.tw/EMC
Korea: https://www.omron-healthcare.co.kr/product/HEM-7157T
Refer to the EMC information for HEM-7157T on the website.
8. Guidance and Manufacturer’s Declaration
• This blood pressure monitor is designed according to the European Standard EN 1060, Non-invasive sphygmomanometers Part 1: General
Requirements and Part 3: Supplementary requirements for electromechanical blood pressure measuring systems.
• Hereby, OMRON HEALTHCARE Co., Ltd., declares that the radio equipment type HEM-7157T is in compliance with Directive 2014/53/EU.
• This OMRON product is produced under the strict quality system of OMRON HEALTHCARE Co., Ltd., Japan. The Core component for OMRON
blood pressure monitors, which is the Pressure Sensor, is produced in Japan.
• Please report to the manufacturer and the competent authority of the Member State in which you are established about any serious incident
that has occurred in relation to this device.
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