
83
Printer
Type
Thermal
Resolution
8 (dots/mm)
Printing speed
45 (mm/s)
Paper width
57 (mm)
17.5
Compliance
Item
Compliant with
Classi
fi
cation
Class I (on AC power) and Internally powered (on battery power)
Equipment not suitable for use in the presence of a
fl
ammable anaesthetic
mixture with air or with oxygen or nitrous oxide.
Mode of operation
Continuous
Type of protection
Type BF – Applied parts (NIBP De
fi
brillation-proof applied parts)
General Safety
93/42/EEC Medical Device Directive
US FDA 21 CFR 820 Code of federal regulations, Quality system
regulation
91/157/EEC Battery Declaration Directive
93/86/EEC Battery Disposal Directive
2006/66/EC Battery directive
2002/96/EC waste electrical and electronic equipment (WEEE)
ISO13485:2003 Quality Systems - Medical devices - Requirements for
regulating purposes
IEC60601-1:1998+A1:1991+A2:1995
General requirements for safety of medical electrical equipment
Speci
fi ca
tions
Содержание Smartsigns Liteplus
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