Product Manual

Manual Information
2040604-012D SEER
®
Light 1-11
system configuration must meet the requirements of the EN/IEC 60601-
1-1 medical electrical systems standard.
The use of ACCESSORY equipment not complying with the equivalent
safety requirements of this equipment may lead to a reduced level of
safety of the resulting system. Consideration relating to the choice shall
include:
 use of the accessory in the PATIENT VICINITY/ENVIRONMENT;
and
 evidence that the safety certification of the ACCESSORY has been
performed in accordance with the appropriate EN/IEC/UL 60601-1
(medical) or EN/IEC/UL 60950 (information technology), and EN/
IEC 60601-1-1 safety standard(s).
Classification
The SEER Light Connect is classified according to EN/IEC 60950.
The SEER Light recorders and controllers are classified, according to
EN/IEC/UL 60601-1, as:
Type of protection against electrical shock Internally Powered Equipment
Degree of protection against electrical
shock
Type B Equipment
Degree of protection against harmful
ingress of water
Ordinary Equipment (enclosed equipment without protection against ingress of water)
Degree of safety of application in the
presence of a flammable anesthetic
mixture with air or with oxygen or nitrous
oxide
Equipment not suitable for use in the presence of a flammable anesthetic mixture with
air or with oxygen or nitrous oxide
Method(s) of sterilization or disinfection
recommended by the manufacturer
Not applicable
Mode of operation Continuous operation