POC-WP21 Series User Manual iv
9. Improper installation of VESA mounting can result in serious personal injury!
VESA mount installation should be operated by professional technician, please
contact the service technician or your retailer if you need this service. The detail
operating procedure is specified in Appendix A.
10. Classification:
1). Supply Class I adapter
2). No applied part
3). IPX1
4). Continuous Operation
5). Not AP or APG category
11. Environmental protection: follow national requirements to dispose of unit.
12. Maintenance: to properly maintain and clean the surfaces, use only the
approved products or clean with a dry applicator.
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 ensur-
ing 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.)
Furthermore all configurations shall comply with the system standard IEC
60601-1-1. Anyone who connects additional equipment to the signal input part
or signal output part is configuring a medical system, and is therefore, responsi-
ble 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 out-
side of the patient environment. If in doubt, consult the technical services
department or your local representative.
Warning! This device is not suitable for use in the presence of flammable anes-
thetic mixture with air, oxygen, nitrous oxide, or for life support systems.
Caution! When servicing the device, always use replacement parts that are quali-
fied 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.