Copyright © 2013, Condor Instruments Ltda.
5
Av. Brigadeiro Luis Antonio, 551, cj 124 - Cep:01318-000
Introduction
Before using the device, read the user manual as a whole.
Indications of Use
The ActTrust is an ultra-compact, lightweight, wrist-worn activity, temperature and ambient light monitor that can
be used to analyze circadian rhythms, automatically collect and store data for sleep parameters, and assess
activity in any instance where quantifiable analysis of physical motion is desirable. The device is intended to
monitor limb or body movements during daily living and sleep.
Contraindications
There are no contraindications to the use of the device.
Adverse Effects
Patients should inform your doctor and discontinue use immediately if they experience itching or irritation in the
contact area of the device with the skin.
Maintenance
Sterilization is not required for nay part of the product.
PRECAUTIONS
Inspections and repairs should only be performed by an authorized agent. Under no circumstances should you
attempt to open or personally carry out repairs or maintenance of the device.
This product must be inspected by a Condor authorized service center five years from the date of manufacture,
before that, the device is intended to provide a safe and reliable operation provided that it is operated and
maintained in compliance with the instructions provided by Condor. The details concerning the Condor warranty
applicable are provided with the device from its original purchase. Of course, like all electrical devices, be careful
and request inspection at a Condor authorized service center if any malfunctions are detects.
Warnings and General Precautions
Warnings
A
warning
to the possibility of personal injury.
•
Before using the device, read the entire manual.
•
The device and its accessories must be used only for the purpose for which they are intended.
•
Only use accessories and parts that are original and approved by Condor.
Additional equipment connected to medical electrical equipment must comply with the respective IEC or ISO
standards (p. Ex., IEC 60950 relating to data processing equipment). In addition, all configurations must meet
the requirements for medical electrical systems (see IEC 60601-1-1 or clause 16 of the 3rd Ed. Of IEC 60601-1,
respectively). Anyone who connects additional equipment to medical electrical equipment configures a medical
system and is therefore responsible for the system to comply with the requirements for medical electrical
systems. It called attention to the fact that local laws take precedence over the above requirements. If in doubt,
contact your local representative or service department.
Training and Qualification
Any operator must have read the manual and have the computer skills necessary to configure the device
The analysis should only be made by people who are qualified to make them
