ActiGraph LLC 03 Manual Do Utilizador
actigraphcorp.com
49 E. Chase Street Pensacola, FL 32502
tel (850) 332-7900
fax (850) 332-7904
TAS14DOC07 User’s Manual
Page 6 of 21
Important Information and Symbols
The ActiGraph Link abides by the following regulations listed below and gives explanation into the
symbols that are found on each device.
symbols that are found on each device.
CAUTION: The battery is to only be changed by trained ActiGraph personnel. The battery
is only allowed to be connected in a certain manner and any incorrect replacement can
result in a hazard.
The devices are compliant with IEC (International Electrotechnical Commission) standards
for "Type BF Applied Part" - meaning they comply with requirements for user protection
against electrical shock. The housing of the device is the only part that is to come into
contact with the end user and is made out of Polycarbonate and/or Polyvinyl Chloride
materials. If you have any allergic reactions to Polycarbonate and/or Polyvinyl Chloride
materials, please consult your doctor before using an ActiGraph device.
CAUTION: Do not simultaneously wear and charge, service, or provide any maintenance
on the device. The end user should not be in the patient vicinity when being charged
CAUTION: Transporting or operating these devices outside of the temperature range of
-10
o
C to +55
o
C could lead to dangerous conditions and/or incorrect data collection.
CAUTION: Modification to ActiGraph devices is not permitted and will void all warranties
if tampered and/or modified. Do not modify the device in any way.
CAUTION: Do not swallow any part of this device. If a piece has been swallowed, contact
your local poison control hotline or seek medical attention as soon as possible.
NOTICE: Device does not have any contraindication(s)
NOTICE: Only use a USB 2.0 cable to connect to the charger. Only use ActiGraph’s
approved USB hubs to charge the device. Do not connect the device to anything else but
a computer and an ActiGraph approved USB hub.
NOTICE: No precautions need to be taken in the event of changes in the performance of
the device.
Class II medical device
1
A patient vicinity is areas in which PATIENTS are normally cared for and the space with surfaces likely to be contacted by the
PATIENT or an attendant who can touch the PATIENT. This encloses a space within the room 1,83 m (6 feet) beyond the perimeter
of the bed (examination table, dental chair, treatment booth, and the like) in its intended location, and extending vertically 2,29 m (7-
1/2 feet) above the floor.
of the bed (examination table, dental chair, treatment booth, and the like) in its intended location, and extending vertically 2,29 m (7-
1/2 feet) above the floor.