Digicare Biomedical Technology
Operators Manual Multi-parameter Patient Monitor " LifeWindow Lite LW8 "
3
• Two Temperature channels;
• Two Invasive Pressure channels;
• Pulse (from SpO
2 ,
NIBP, IP1 or IP2) rate;
• NIBP Systolic, Diastolic and mean arterial pressure;
• End-tidal CO2 concentration (EtCO2) – Mainstream or Sidestream;
• Inspired CO2 concentration (inCO2) – Mainstream or Sidestream;
• Respiration rate (from EtCO2 waveform);
• Inspired Fraction of O2 ( FIO2 );
CONFIGURATION CODE
Electrocardiogram – 3 Lead ECG........................................................................................ E
Electrocardiogram – 5 Lead ECG.......................................................................................5E
Pulse Oximetry and Plethysmogram ................................................................................. S
FIO2 – Inspired Fraction of Oxygen ................................................................................. F
CO2 - Sidestream Capnography .................................................................................
C
CO2 - Mainstream Capnography .............................................................................
M
CO2 DualCap – Mainstream and Sidestream Capnography .............................................. D
Non-invasive Blood Pressure - NIBP ..........................................................................
N
Invasive Pressure (up to two channels) .........................................................................
#P
Temperature (up to two channels) ...................................................................................... #T
The applied parts are classified accordingly to the degree of electrical isolation from the patient
and defibrillation protection.
• The ECG patient connection is DEFIBRILLATION PROOF type CF applied part.
• The Invasive Pressure connection is type CF applied part and is not DEFIBRILLATION
PROOF.
• The Temperature connection is type BF applied part and is not DEFIBRILLATION PROOF.
• The SpO2 is type BF applied part and is not DEFIBRILLATION PROOF.
• All other patient connections are NOT DEFIBRILATION PROOF type B applied part.
2 - CAUTIONS
The LifeWindow™ Lite LW8 was designed and tested accordingly to the ELECTRO-MAGNETIC
COMPATIBILITY Standard IEC601-1-2. However, the operator is responsible to verify if the
monitor is been affected or affecting others electrical equipment. Equipments like electrocautery
and image scanners can generate interference and cause degradation of the
LifeWindow™ Lite LW8 performance. To avoid this situation, it should be installed as far as
possible of those equipment.
3- CONTRAINDICATIONS
The LifeWindow™ Lite LW8 series is NOT intended to be used during MRI (magnetic
resonance imaging).
The LifeWindow™ Lite LW8 is NOT suitable for use in the presence of a flammable anaesthetic
mixture with air or with oxygen or nitrous oxide.
E. UNPACKING AND ACCESSORIES
Carefully remove the monitor and its accessories form the shipping carton. Save the packing
materials in case the monitor must be shipped or stored. Ensure your LifeWindow
Lite LW8
has the items listed in the SHIPPING LIST inside the carton.
Summary of Contents for LifeWindow Lite LW8
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