Fora DUO ultima D40, Руководство пользователя

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D40 Owner’s Manual
EN-25
Specifications
System performance
Power Source
Four 1.5V AA alkaline batteries or one 3.7V rechargeable
Li-ion battery
Device Dimensions (w/o cuff) 147 (L) x 105 mm (W) x 80 mm (H), 500g with batteries
Memory Maximum 864 memory records
Power Saving
Automatic power off if system idle for 3 minutes (normal
mode) or 5 minutes (RF mode).
System Operating Condition 10°C to 40°C (50°F to 104°F), below 85% RH
Device Storage/Transport
Condition
-20°C to 60°C (-4°F to 140°F), 5 - 95% RH
Power Supply Input DC +6V / 1A (max) via Power Plug
Blood glucose measurement performance
Measurement Unit mg/dL or mmol/L
Linear Range 20 to 600 mg/dL (1.1 to 33.3mmol/L)
Precision ±5 % (CV)
Accuracy
±15 mg/dL (0.83 mmol/L) when glucose < 75mg/dL (4.2
mmol/L)
±20% when glucose
≥
75mg/dL (4.2 mmol/L)
Ketone Warning glucose value is over 240 mg/dL (13.3 mmol/L)
Blood pressure measurement performance
Pressure Range 0 - 300 mmHg
Heart Rate Range 40 -199 beat per minute
Measurement Unit mmHg
Systolic Measurement Range 55 mmHg -255 mmHg
Diastolic Measurement Range 25 mmHg -195 mmHg
Maximum Inflation Pressure 280 mmHg
Accuracy of Pressure ±3 mmHg or ±2% of reading
Accuracy of Pulse Rate ±4% of reading
This device has been tested to meet the electrical and safety requirements of: IEC/EN 60601-1,
IEC/EN 60601-1-2, IEC/EN 61010-1, IEC/EN 61010-2-101, IEC/EN 61326-2-6, EN 301 489-17, EN
300 328.
Reference to Standards:
• EN 1060-1 / EN 1060-3, NIBP-requirements
• IEC 60601-1 General requirement for safety
• IEC 60601-1-2 Requirements for EMC
• EN 1060-4, NIBP clinical investigation
• AAMI/ANSI /IEC 80601-2-30, ANSI/AAMI/ISO 81060-2, NIBP requirements