Omron HEM-7361T, Instruction Manual

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8
EN
Durable period (Service
life)
Monitor: 5 years / Cuff: 5 years /
Optional AC adapter: 5 years
Operating conditions +10 to +40°C / 15 to 90% RH (non-
condensing) / 800 to 1060 hPa
Storage / Transport
conditions
-20 to +60°C / 10 to 90% RH (non-
condensing)
Weight Monitor: approximately 460 g (not
including batteries)
Arm cuff: approximately 163 g
Dimensions
(approximately value)
Monitor: 191 mm (W) × 85 mm (H) ×
120 mm (L) / Arm cuff:145 mm ×
532 mm (air tube: 750 mm)
Cuff circumference
applicable to the monitor
220 to 420 mm
Memory Stores up to 100 readings per user
Contents Monitor, arm cuff (HEM-FL31), 4 “AA”
batteries, Instruction Manual and
, setup instructions, storage case
Protection against electric
shock
Internally powered ME equipment
(When using only batteries)
Class II ME equipment (Optional AC
adapter)
Applied part Type BF (arm cuff)
Maximum temperature of
the applied part
Lower than +43°C
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 (other than HHP-OH01) is protected
against vertically falling water drops which may cause issues during a normal
operation. HHP-OH01 is protected against oblique 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.
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
Asia Pacific: https://www.omronhealthcare-ap.com/emc-information
Korea: https://www.omron-healthcare.co.kr/product/HEM-7361T
Taiwan: https://www.omronhealthcare.com.tw/EMC
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-7361T 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.