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Battery
LI+ (lithium-Ion), 3.0DC non-rechargeable for memory backup and real-time clock power; not a primary power
source when AC power is not present
Environment
The monitor may not meet its performance specifications if stored or used outside the temperature and humidity ranges listed below.
Temperature
Operation:
0 - 50°C (32 – 122°F)
Storage:
40 - 75°C (-40 - 167°F)
Relative humidity
Operation:
15 - 95% (non-condensing)
Storage:
10 – 95% (non-condensing)
EMC
EN 60601-1-2 with scale cables lot code 1103-01 or higher
Languages
Clinician:
English
Patient:
Menu selectable: English Audio (Male and Female voice) and Text
Modem Type:
33.6K baud
Compliance approvals:
FCC Part 15B
FCC Part 68
Connection:
RJ-11
Non-Invasive Blood Pressure
Manufacturer:
SunTech
Method of measurement:
Oscillometric
Blood pressure range:
20 to 260 mmHg (40 – 260 mmHg systolic, 20 – 200 mmHg diastolic)
Pressure Transducer Accuracy; +/- 3 mmHg between 0 mmHg and 300 mmHg, for operating conditions between 0° C and 50° C and less than 95%
relative humidity.
Patient safety:
Maximum cuff inflation time is limited to 50 seconds. Duration of blood pressure reading is limited to 130 seconds.
Redundant safety circuitry aborts reading if cuff pressure exceeds 300 mmHg or if cuff has been inflated for 180
seconds.
Calibration:
Recommended yearly
Safety standards:
Meets all relevant parts of AAMI SP-10-1992, IEC-60601-1, IEC-60601-2-30, EN1060-1, EN1060-3
Initial inflation pressure:
120-250 mmHg adult mode
Default inflation pressure:
175 mmHg (120-280 mmHg)
Oximeter module (optional)
Range:
0 - 99% Functional SpO
Accuracy:
±2 at 70 - 99% less than 70% is unspecified
Alarms:
None
Averaging:
8 pulse beat average
P.4510EN.01
GENESIS DM CLINICAL GUIDE
(1% increments)
2
12/5/2007
Index
79
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