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Philips ST80i - Page 27

Philips ST80i
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Important Patient and Safety Information
ST80i Stress Test System Instructions for Use xv
Ce dispositif doit accepter tout brouillage reçu, y compris un brouillage susceptible de
provoquer un fonctionnement indésirable.
This ISM device complies with Canadian ICES-001.
Cet appareil ISM est conforme à la norme NMB-001 du Canada.
Proper patient preparation is important for proper application of ECG electrodes and
operation of the device.
Use wireless PIM belts and NIBP cuffs appropriate for the patient’s size.
Patient lead sets should be checked for cracks or breakage in its exterior properties prior to
use.
The wireless PIM includes LEDs that indicate battery power level, wireless signal quality,
and lead contact status. When the wireless PIM is powered on, the battery power level
LED is lit. You can click the power button anytime to check the status of the battery,
wireless signal, or lead contacts.
As defined by IEC 60601-1 and IEC 60601-2-25, the device is classified as follows:
Internally powered
Type CF applied parts
Ordinary equipment
Not suitable for use in the presence of flammable anesthetics or flammable mixtures
of air, oxygen, or nitrous oxide
Continuous operation

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