Copyright © 2022, Condor Instruments Ltda. 3
Professor Tulio Street Ascarelli, 290 - Vila Madalena, São Paulo, SP - Cep:05449-020
Introduction
Before using the device, read the manual in its entirety.
Indications for use
ActLumus is an ultra-compact and lightweight monitor of activity, temperature and ambient pulse light that can be
used to analyze circadian rhythms, automatically collect and store data for sleep parameters, and valiate activity
in any instance where quantifiable analysisof physical motion is desired. The device is intended to monitor limb
or body movements during daily life and sleep.
Contraindications
There are no contraindications to the use of the device.
Adverse effects
Patients should tell their doctor and discontinue use immediately in case they experience itching or irritation in
the skin contact area of the device.
Maintenance
Sterilization is not required for any part of the product.
PRECAUTIONS
Inspections and repairsshould only be carried out by an authorised agent. Under no circumstances should you
attempt to open, or personally repair or maintain the device.
This product must be inspected by an authorized Condor service centre five years after the date of manufacture.
Prior to this, the device is intended to provide safe and reliable operationprovided that its use and maintenance
complies with the instructions provided by Condor. Details regarding the applicable Condor warranty are provided
with the device from your original purchase. Obviously, like all electrical devices, you should be careful and request
inspection of the device at a Condor authorized service center if you detect anomalies in it.
General Warnings and Precautions
Notices
Thevision for the possibility of bodily injury.
• Before using the device, read the manual in its entirety.
• The device and accessories should only be used for the purpose for which they are intended.
• Use only original and Condor approved accessories and parts.
Additional equipment connected to electrical medical equipment must comply with the respective IEC or ISO
standards (e.g. IEC 60950 for data processing equipment). In addition, all configurations must meet the
requirements for electrical medical systems (see IEC 60601-1-1 or clause 16 of the 3rd ed. of IEC 60601-1,
respectively). Anyone who connects additional equipment to electrical medical equipment configures a medical
system and is therefore responsible for the system meeting the requirements for electrical medical systems.
Attention is drawn to the fact that local legislation has precedence over the above-mentioned requirements. If in
doubt, consult your local representative or technical assistance department.
WARNING: The use of this adjacent equipment or other equipment should be avoided, as it may result in improper
operation, If this use is necessary, it is advisable that this and the other equipment be observed to verify that they
are operating normally
WARNING: The use of accessories, transducers and cables other than those specified or supplied by the
MANUFACTURER of this equipment could result in high electromagnetic emissions or reduced electromagnetic
immunity from this equipment and result in improper operation
WARNING: Portable RF communication equipment (including peripherals such as antenna cables and external
antennas) should not be used within 30 cm of any part of the (EQUIPMENT IN OR IN SYSTEM), including cables
specified by the MANUFACTURER, otherwise performance degradation of this equipment may occur
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