Chapter 1: Introduction
Advisor
®
Service Manual 1-3
Z
Collect
separately
Disposal (EU Countries)
Under the Waste Electrical and Electronic Equipment (WEEE) Directive 2006/96/EC and
implementing regulations, all devices and service items within the scope of the Directive
purchased new after August 13, 2005 must be sent for recycling when ultimately becoming
waste. Devices and items must not be disposed of with general waste.
If purchased before that date, they may also be sent for recycling if being replaced on a
one-for-one, like-for-like basis (this varies depending on the country). Recycling instructions
to customers using Smiths Medical products are published on the internet at:
http://www.smiths-medical.com/recycle
Y
Disposal (other countries)
When disposing of this device, its batteries or any of its accessories, ensure that any
negative impact on the environment is minimized. Contact your local waste disposal service
and use local recycling or disposal schemes. Separate any other parts of the equipment
where arrangements can be made for their recovery; either by recycling or energy recovery.
The main batteries are potentially harmful and will require separate disposal according to
manufacturer’s instructions or local regulations.
Note: If applicable, EU, national or local regulations concerning waste disposal must
take precedence over the above advice.
KEYWORD
DEFINITION
WARNING
Tells you about something that could hurt the patient or hurt the operator
CAUTION
Tells you about something that could damage the monitor
NOTE
Tells you other important information
General Warnings, Cautions, and Notes
WARNING! Do not use this device in the presence of ammable anesthetics.
WARNING! ELECTRICAL SHOCK HAZARD when covers are removed. Unit is not user serviceable.
7
Refer servicing to qualied personnel.
WARNING! Do not plug the monitor into an outlet controlled by a wall switch.
WARNING! This device is intended for use by trained healthcare professionals. The operator must be
thoroughly familiar with the information in the operation manual before using the device.
WARNING! This monitor is not for apnea detection. The monitor has not been tested or validated for use
in apnea detection.
WARNING! This monitor is not for home use.
WARNING! Verify proper operating mode before attaching patient. See Select the Patient Type in the
1886R operation manual Chapter 3: Setting Up the Monitor.
WARNING! Do not use this device in the presence of magnetic resonance imaging (MR or MRI)
equipment.
WARNING! Operation of this device may be adversely aected in the presence of computed tomography
(CT) equipment.
WARNING! Operation of this device may be aected in the presence of strong portable and mobile
communications equipment.
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