approved products or clean with a dry applicator.
Caution!
When servicing the device, always use replacement parts that are
qualified to Advantech standards. Advantech Digital Healthcare cannot
war-rant or endorse the safe performance of third-party replacement
parts for use with our medical device.
13.
Make sure the user does not allow contact between SIP/SOPs and the patient
at the same time.
14.
When networking with electrical devices, the operator is responsible for
ensuring that the resulting system meets the requirements set forth by the
following standards:
–
EN 60601-1 (IEC 60601-1)
Medical electrical equipment
Part 1: General requirements for safety
–
EN 60601-1-1 (IEC 60601-1-1)
Medical electrical equipment
Part 1-1: General requirements for safety
Collateral standard: Safety requirements for Medical electrical systems
–
EN 60601-1-2 (IEC 60601-1-2)
Medical electrical equipment
Part 1-2: General requirements for safety
Collateral standard: Electromagnetic compatibility; Requirements and tests
15.
Accessory equipment connected to analog and digital interfaces must be in
compliance with the respective nationally harmonized IEC standards (i.e. IEC
60950 for data processing equipment, IEC 60065 for video equipment, IEC
61010-1 for laboratory equipment, and IEC 60601-1 for medical equipment.)
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