Aeon A310L Manual De Usuario página 5

used no closer than 30 cm (12 inches) to any part of the A310L Pulse Oximeter, including cables specified by the
manufacturer. Otherwise, it may result in a degradation of the performance of this equipment.
High-pressure sterilization cannot be used on the device.
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IF ANY: a list of all cables and maximum lengths of cables (if applicable), transducers and other accessories that are

replaceable by the responsible organization and that are likely to affect compliance of the me equipment or me system
with the requirements of clause 7 (emissions) and clause 8 (immunity). accessories may be specified either generically
(e.g., shielded cable, load impedance) or specifically (e.g., by manufacturer and equipment or type reference).
IF ANY: the performance of the me equipment or me system that was determined to be essential performance and a

description of what the operator can expect if the essential performance is lost or degraded due to em disturbances (the
defined term "essential performance" need not be used).
Cautions:
Keep the operating environment free of dust, vibrations, corrosive, or flammable materials, and extremes of temperature

and humidity.
Do not operate the unit, if it is damp or wet because of condensation or spills. Avoid using the equipment immediately

after moving it from a cold environment to a warm, humid location.
Never use sharp or pointed objects to operate the front-panel switches.
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The batteries must be taken out from the battery compartment, if the device will not be used for a long time.
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The device shall only be used with the battery cover closed.
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The batteries must be disposed of properly, according to local regulation after their use.
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Keep the device away from children and pets to avoid swallowing.
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1.3 Definitions and Symbols
Symbol
Type BF Equipment
Indicates the item is a medical device
Information of manufacturer, including name and
address
Temperature limitation
For its disposal, this product must be sent to
separate collection facilities for recovery and
recycling
Follow the instructions for use
Cautions ： The information you should know to protect the equipment from possible damage.
Note ： The important information you should know.
Warning ： The information you should know to protect patients and medical staff from possible injury.
ME Medical Electronics Equipment.
Note: [1][2][3] Batch code, Date of manufacture and Serial No. are printed on the label on the battery cover.
2 Introduction
2.1 Intended use
The A310L Pulse Oximeter is a non-invasive device intended for spot checking of functional oxygen saturation of arterial
hemoglobin (SpO ) and pulse rate (PR). This portable device is suitable for non-professional adult patients of any color in
2
Table 3: Description of symbol
Description
5
Symbol Description
Batch code [1]
Indicates a carry that contains unique
device identifier information
Date of manufacture
Serial No.
[3]
Information
representative
IP22
Anti-dust & Anti-water class
English
[2]
of EU authorized