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Smeg WD2145
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User Manual
WD2145-WD1160-WD4060-WD4190
Page 71 - 85
ELECTRICITY SUPPLY
MODEL
ELECTRICITY SUPPLY
INTEGRAL PROTECTIVE
DEVICES
Max voltage/power
There are three possible electrical
versions.
60cm models: The names of the models have
different suffixes to identify the power supply rating.
E.g. If the model does not have a suffix, e.g.
“WD4060” it will be three-phase, with neutral, 400V
between phases.
“WD4060-3” indicates three-phase model, 230V
between phases, no neutral.
“WD4060-1” indicates single-phase model.
WD2145
230V ~ / 50Hz / 14A / 3300W
FUSES 10.3x38 16 A ON POWER
SUPPLY
[L1, N]
WD2145,
variant cod.
860476 (UK
market)
230 V ~ / 50Hz / 13A /
3000W
FUSES 10.3x38 16 A ON
POWER SUPPLY
[L1, N] + 13 A “BS1362” FUSE
incorporated in UK “BS1363”
plug.
WD1160
WD4060
WD4190
400V 3N~ / 50Hz / 12A /
7000W
FUSES 10.3x38 16 A ON
POWER SUPPLY
[L1, L2, L3]
WD1160-3
WD4060-3
WD4190-3
230V 3~ / 50Hz / 19A /
7000W
FUSES 10.3x38 20 A ON POWER
SUPPLY
[L1, L2, L3]
WD1160-1
WD4060-1
WD4190-1
230V 1N~ / 50Hz / 12A /
2800W
FUSES 10.3x38 16 A ON POWER
SUPPLY
[L1, N]
OTHER DATA
DATA COMMUNICATION - PRINTER
CONNECTION
RS-232 PORT
MAX. NOISE LEVEL
50dB
AMBIENT CONDITIONS
USE
Indoor
ALTITUDE
Up to 1000m
AMBIENT TEMPERATURE
From 5°C to 40°C
MAX RELATIVE HUMIDITY
80% for temperatures up to 31°C with linear decrease to
50% at the temperature of 40°C
INSTALLATION CATEGORY (OR SURGE CATEGORY or
INSTALLATION CATEGORY)
II
ELECTRICAL INSULATION CLASS (ref. IEC 61140)
I
DEGREE OF POLLUTION
2 (ref. 61010-1, point 3.6.6.2)
STANDARDS AND CLASSIFICATION
CONFORMITY
- European directive 2006/95/CE [Safety]: European Standard EN61010-1:2001,
EN61010-2-040:2005
- European directive 2004/108/CE [Emc] : European Standard EN61326:2006
- European directive 2011/65/CE [RoHS 2] : European Standard EN 50581:2012
- European directive 93/42/CE, 2007/47/CE [MD]: European Standard
EN ISO 14971:2012, EN 62304:2006, EN62366:2008, EN ISO 15883-1:2009, EN
ISO 15883-2:2009
- Other: European Standard EN 61770:2009
MEDICAL DEVICE CLASSIFICATION WD
family only
class IIb medical devices (in accordance with the classification criteria
established by Directive 93/42 and subsequent additions and amendments,
extended and amended by EC Directive 2007/47).

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