Barco MDRC-2122 WP, Руководство пользователя

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7. Important information
To fully disengage the power to the device, please disconnect the power cord from the AC inlet.
Power cords:
• Do not overload wall outlets and extension cords as this may result in fi re or electric shock.
• Mains lead protection (U.S.: Power cord): Power cords should be routed so that they are not likely to
be walked upon or pinched by items placed upon or against them, paying particular attention to cords
at plugs and receptacles.
• The power supply cord should be replaced by the designated operator only at all time.
• Use a power cord that matches the voltage of the power outlet, which has been approved and complies
with the safety standard of your particular country.
Grounding reliability
Grounding reliability can only be achieved when the equipment is connected to an equivalent receptacle
marked “Hospital Only” or “Hospital Grade” (located on product or power supply cord)
External equipment
External equipment intended for connection to signal input/output or other connectors, shall comply with
relevant UL/ EN/ IEC standard (e.g. UL/EN/IEC 60950 for IT equipment and UL/EN 60601-1 / IEC 60601
series for medical electrical equipment). In addition, all such combinations -systems- shall comply with the
standard IEC 60601-1-1, safety requirements for medical electrical systems. Equipment not complying
with UL/EN / IEC 60601-1 shall be kept outside the patient environment, as de
fi ned in the standard.
Equipment not complying with IEC 60601 must be kept outside the patient environment, as de fi ned in the
standard as at least 1.5 meters from the patient or the patient support.
Any person who connects external equipment to signal input, signal output, or other connectors has formed
a system and is therefore responsible for the system to comply with the requirements of IEC 60601-1-1.
If in doubt, speak with a quali
fi ed technician.
In locations where 240 V outlets are used, connect this display only on a center-tapped, 240 V, single-
phase supply.
Water and moisture
Never expose the device to rain or moisture. Never use the device near water - e.g. near a bathtub,
washbasin, swimming pool, kitchen sink, laundry tub or in a wet basement.
IP-x level for MDRC-2122 BL: Ordinary
IP-x level for MDRC-2122 WP and MDRC-2122 TS: Protection glass, IP32
Ventilation
Do not cover or block any ventilation openings in the cover of the set. When installing the device in a
cupboard or another closed location, heed the necessary space between the set and the sides of the
cupboard.
Installation
Place the device on a fl at, solid and stable surface that can support the weight of at least 3 devices. If you
use an unstable cart or stand, the device may fall, causing serious injury to a child or adult, and serious
damage to the device.
This apparatus conforms to:
CE (MDD 93/42/EEC class I product), CE-2004/108/EC, 2014/30/EU (Directive 2004/108/EC is repealed
with effect from 20 April 2016), IEC 60950-1:2005 + A1:2009 (2ND EDITION), IEC 60601-1 2ND ED:1988
+ A1:1991 + A2:1995, IEC 60601-1:2005 + A1:2012, ANSI/AAMI ES 60601-1:2005 + C1:2009 + A1:2012,
CAN/CSAC22.2 No. 60601-1-08:2008, DEMKO - EN 60601- 1:2006, EN 60601-1-2:2007, EN 60601-
1:2006+A11:2011, CCC - GB9254-2008 + GB4943-2001 + GB17625.1-2003 (MDRC-2122 BL and MDRC-
2122 WP only), KC, VCCI, FCC class B, ICES-001 Level B, FDA Class I device, RoHS
24 K5903049 EONIS 25/06/2015