HID-2334 User Manual
HID-2334 Quick Reference Guide
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10. Environmental protection: follow national requirements to dispose of unit.
11. Maintenance: to properly maintain and clean the surfaces, use only the approved
products or clean with a dry applicator.
12. Make sure the user not to contact SIP/SOPs and the patient at the same time.
13. 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
14. 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 60601-1 certified equipment outside of the patient environment. If in doubt,
consult the technical services department or your local representative.
