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This system comply with following EMC/EMI standards:
EN 60601-1-2:2007+AC:2010: Electromagnetic Compatibility
Emission: CISPR 11:2009+A1:2010, Class B
Immunity: IEC 61000-4-2:2008, IEC 61000-4-3:2010, IEC 61000-4-4:2012,
•
If you encounter technical problems with the monitor, contact a qualified
service technician or your retailer.
•
Users must not allow SIP/SOPs and the patient to come into contact at the
same time.
•
Grounding reliability can only be achieved when the equipment is connected to
an equivalent receptacle marked "Hospital Only" or "Hospital Grade".
•
The Mains isolation is by AC power supply cord.
•
Use a power cord that matches the voltage of the power outlet, which has been
approved and complies with the safety standard of your particular country.
•
WARNING - Do not modify this equipment without authorization of the
manufacturer.
•
WARNING: To avoid risk of electric shock, this equipment must only be
connected to a supply mains with protective earth.
•
CAUTION: Use suitable mounting apparatus to avoid risk of injury.
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Explanation of the graphical symbols:
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Classification
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Supplied by Class I power
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No applied parts
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No protection against the ingress of water: IPX0
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Mode of operation: Continuous Operation
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The equipment is not suitable for use in the presence of a flammable
anesthetic mixture with air or oxygen or nitrous oxide: Not AP or APG
category
vi
AS/NZS CISPR 11:2011
EN 61000-3-2:2006+A1:2009+A2:2009 and EN 61000-3-3:2008
IEC 61000-4-5:2005, IEC 61000-4-6:2008, IEC 61000-4-8:2009,
IEC 61000-4-11:2004
WARNING: Dangerous voltage.
ATTENTION: consult ACCOMPANYING DOCUMENTS.
Follow operating instructions or Consult instructions for use.
STAND-BY.
Direct current.
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