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Omron HBP-1320 - Key Product Features; Unit Functions and Controls; Front and Back Unit Overview

Omron HBP-1320
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11
PM-1795-01-06/2018
EN 60601-1-6:2010+A1 :2015
EN 80601-2-30:2010+A1 :2015
EN 62304:2006+A1:2015
EN 62366:2008+A1:2015
EN ISO 10993-1:2009/AC:2010
EN ISO 10993-5:2009
EN ISO 10993-10:2013
EN ISO 14971:2012
EN ISO 81060-2 :2014
EN ISO 13485 :2016
2011/65/EU Restriction of Hazardous Substances (RoHS) : EN 50581 :2012
Operation and care
Cleaning and disinfecting should be performed in accordance with your facility’s
infection control practice.
Cleaning of the device
Wipe with a cloth that has been moistened with isopropyl alcohol diluted to 50 v/v%,
or ethyl alcohol (disinfection alcohol) diluted to 80 v/v% or less and wrung out.
Do not wipe the DC jack or allow it to become wet.
Warnings
The warning signs and symbol examples indicated below are intended to ensure safe
use of the product and prevent damage and injury to you and others. The signs and
symbols are explained below.
Warning: Indicates the matters in which death or severe bodily damage may arise as
a result of incorrect handling.
Caution: Indicates the matters in which bodily harm or material damage may arise as
a result of incorrect handling.
Storage/Setup
Warnings
• Install the unit in a location close to a power outlet where the AC adapter can be
easily disconnected. If the power cannot be quickly disconnected when an abnormal
condition occurs, an accident or fire may result.
• Do not use the cuff or AC adapter to lift the unit, it can also cause the unit to
malfunction.
• If the unit has broken down, contact your OMRON retail dealer or distributor.
• Do not use in combination with a hyperbaric oxygen therapy device, or in an
environment where combustible gas may be generated.
• Do not use in combination with magnetic resonance imaging (MRI) equipment. If
MRI is to be performed, remove cuff connected to the unit from the patient.

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