Amico ice 30m, Инструкция по установке и эксплуатации

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Installation Considerations
• All Amico lamps are supplied with a flange with a graduated circle diameter of 310 mm (12.2") and six bores with
a diameter of 17 mm (0.67"). The flange supports the vertical suspension tube. It is attached to the solid ceiling
by means of a ceiling anchorage ring.
• The ceiling anchorage plate has six precisely positioned M16 threaded bolts. This makes it possible to fasten and
adjust the lamp without causing dust or dirt after all building work has been completed.
• The ceiling anchorage ring is not required for a combination pendant and LED configuration.
• During mounting, take care to ensure that neither the flange nor the attachment elements are in contact with
reinforcement components of the solid ceiling.
• The forces arising when the widely extending articulated arms tilt do make it necessary to drill very carefully with
a certified hammer drill, paying close attention to the drilling tolerances.
• The suspension tube of the lamp or lamp combination must be adjusted vertically to prevent the lamp body
from moving. For this purpose, the M16 counter nuts on the attaching bolt must be adjusted accordingly.
• For false ceilings, the suspension tubes for all lamps can be mounted directly through to the solid ceiling. The
opening required for this purpose can be closed once the work has been completed. This can be completed by
using the ceiling cover with a diameter of 450 mm (17.7") or a covering plate.
• Amico Clinical Solutions Corp. can only be made responsible for the safety of the light if repairs and alterations
are carried out by Amico Clinical Solutions Corp. or a company that guarantees to observe the safety regulations.
• Amico Clinical Solutions Corp. cannot be made liable for personal or material damages if the light is operated
inexpediently or incorrectly or used for purposes other than those for which it is intended.
• Please read the instructions carefully to install your lighting system and to avoid any damages to the device. Pay
attention to the instructions for use when handling the lamp.
• This device has not been designed for use in potentially explosive areas. According to the Medical Device
Regulation the light is classified under class I in Canada and class II in US per FDA.
• This device requires connection to a back-up system (done on site and provided by the facility) in the event
of interruption of the supply mains for safety service. The back-up system shall restore power within five (5)
seconds.