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Safety Information
Equipment Classification
As per the International Electrotechnical Commission standard IEC 60601-1,
and the European standard EN 60601-1, Medical Electrical Equipment, General
Requirements for Safety, the NeuroMove® is classified as follows:
Type BF Equipment
A Type BF piece of equipment is one that provides a particular degree
of protection against electric shock, particularly regarding allowable
leakage current. A Type BF applied part is one that is floating above
ground and is isolated from all other parts of the equipment.
Internally Powered Equipment
The NeuroMove® is classified as an internally powered device. Note:
Use only with supplied battery charger:
Input range: 100-240 VAC, 50-60 Hz. Output: 12 VDC, 500 mA.
Electromagnetic Compatibility
Conforms to IEC 60601-1-2.
Temperature
Operating temperature range: 0° - 50° C (32° - 122° F)
Storage temperature range: -20° - 70° C (-4° - 158° F)
Humidity
Operating relative humidity range: 0-95%, non-condensing
Transport and storage relative humidity range: 0-95%, non-condensing
Pressure
Operating pressure range: 500-1060 hPa
Transport and storage pressure range: 500-1060 hPa
Water Ingress
Ordinary equipment. This device has protection against
ingress of water.
Flammable Anesthetics
This device is not suitable for use in the presence of a flammable
anesthetic mixture with air, or in the presence of a flammable
anesthetic mixture with oxygen or nitrous oxide.
Disinfection
The enclosure and patient cable may be disinfected and cleaned with
a 70% isopropyl alcohol solution.
