Tyco Electronics ET1528L - Manual (Page 40)

cabling may compromise electrical safety or CE Mark
Certification for emissions or immunity as required by the
following standards:
This Medical Electrical Equipment is required to have a
CE Mark on the manufacturer’s label which means that
the equipment has been tested to the following Directives
and Standards:
This equipment has been tested to the requirements for
the CE Mark as required by medical device Directive
(MDD) 93/42/EEC indicated in European Standard
EN60601-1 and EN60601-1-2 (including EN55011 Class
B).
D) General Information to all Users: This equipment
generates, uses and can radiate radio frequency energy. If
not installed and used according to this manual the equipment
may cause interference with radio and television
communications. There is, however, no guarantee that
interference will not occur in any particular installation due
to site-specific factors.
1) In order to meet emission and immunity requirements,
the user must observe the following:
a) Use only the provided I/O cables to connect this
digital device with any computer.
b) To ensure compliance, use only the provided
manufacturer’s approved power cord.
c) The user is cautioned that changes or modifications
to the equipment not expressly approved by the party
responsible for compliance could void the user’s
authority to operate the equipment.
2) If this equipment appears to cause interference with
radio or television reception, or any other device:
a) Verify as an emission source by turning the
equipment off and on.
b) If you determine that this equipment is causing the
interference, try to correct the interference by using
one or more of the following measures:
i) Move the digital device away from the affected
receiver.
ii) Reposition (turn) the digital device with respect
to the affected
receiver.
iii) Reorient the affected receiver’s antenna.