7. Important information
Power cords:
• Utilize a UL-listed detachable power cord, 3-wire, type SJ or equivalent, 18 AWG min., rated 250 V
min., provided with a hospital-grade type plug 5-15P configuration for 120V application, or 6-15P for
240V application.
• Do not overload wall outlets and extension cords as this may result in fire 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.
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 defined in the standard.
Equipment not complying with IEC 60601 must be kept outside the patient environment, as definedinthe
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 qualified technician.
In locations where 240 V outlets are used, connect this display only on a center-tapped, 240 V, single-
phase supply.
Wa ter 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 fo r MDRC-2122 WP: 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 flat, 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/ 10
8/EC, IEC 60950-1:2005 + A1:2009 (2ND EDI-
TION), IEC 60601-1 2ND ED:1988 + A1:1991 + A2:1995, UL 60601-1 1ST EDITION, CAN/CSA-C22.2
NO. 601.1-M90:2005, 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, CCC - GB9254-
2008 + GB4943-2001 + GB17625.1-2003, KC, VCCI, FCC class B, ICES-001 Level B, FDA Class I de-
vice, RoHS
National Scandinavian Deviations for CL. 1.7.2:
Finland: "Laite on liitettävä suojamaadoituskoskettimilla varustettuun pistorasiaan"
24
K5903049 EONIS 19/02/2014
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