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WMP-226(V)/227(V) User’s manual
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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
Accessory equipment connected to
the 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.) Furthermore all configurations shall comply with the
system standard IEC 60601-1-1. Everybody who connects
additional equipment to the signal input part or signal output part
configures a medical system, and is therefore, responsible that
the system complies with the requirements of the system
standard IEC 60601-1-1. The unit is for exclusive interconnection
with IEC 60601-1 certified equipment in the patient environment
and IEC 60XXX certified equipment outside of the patient
environment. If in doubt, consult the technical services
department or your local representative.