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• Protection Class: Class I
(8) Operating Environment
• Room Temperature:
• Relative Humidity:
• Altitude:
• Pollution:
• Installation Category
(Overvoltage Category):
• For indoor use only.
(9) Storage and Transport Environmental Conditions
• Temperature:
• Humidity:
(10) Conforming Standards
• The model for 100, 110 and 120 V areas is a UL-listed product.
• The model for 220,230 and 240 V areas satisfies the EU IVD Directive (In vitro diagnostic medical
device directive).
(GM approved product : In vitro diagnostic medical device)
• The model for 220, 230 and 240 V areas satisfies the EU LV Directive (Low Voltage Directive).
• The model for 220, 230 and 240 V areas satisfies the EU EMC Directive. (EN 61326)
Chapter 10 Technical Specifications
Model for 220, 230, 240 V Areas
• Input voltage:
Select from 220 V, 230 V or 240 V AC by relocating
the fuse holder in the AC inlet.
• Frequency:
50/60 Hz
• Voltage fluctuation: ±10%
• Rated current:
0.4 A max.
• Fuse rating:
250 V, 1A, time-lag low-breaking type, 5×20 miniature
fuse ×2
• Power Cord:
Use only the following power supply cord. Using the
wrong power cord could result in danger or fire.
The protection Class I equipment should be connected
to PE (protective earth) terminal.
• Approved according to EU/EN standards,
0° to 40°C
85% Max. No condensation should form.
2000 m Max.
Degree 2
Category 2
-20° to +60°C
max. 90%RH (non-condensing)
(The model for 100, 110 and 120 V areas is not covered by the FCC.)
86
3 conductor grounding Type H05VV-F, 3 m long
maximum, rated at 250 V AC minimum.
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