Omron JPN750 Instruction Manual page 9

Note
• These specifications are subject to change without notice.
• This monitor is clinically investigated according to the requirements of EN ISO 81060-2:2014 and complies with EN ISO 81060-2:2014 and
EN ISO 81060-2:2019+A1:2020. In the clinical validation study, K5 was used on 85 subjects for determination of diastolic blood pressure.
• This monitor has not been validated for use on pregnant patients.
• 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 HHP-CM01 is protected against vertically
falling water drops which may cause issues during a normal operation. The optional AC adapters HHP-OH01, HHP-BH01 and HHP-BFH01 are
protected against oblique falling water drops which may cause issues during a normal operation.
• Operation mode classification complies with IEC 60601-1.
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.
7. Important Information regarding Electromagnetic Compatibility (EMC)
This device conforms to the EN 60601-1-2:2015 Electromagnetic Compatibility (EMC) standard.
Further documentation in accordance with this EMC standard is available at
https://healthcare.omron.com/electro-magnetic-compatibility
8. Guidance and Manufacturer's Declaration
• This blood pressure monitor 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 product is produced under the strict quality system of OMRON HEALTHCARE Co., Ltd., 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.
EN
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