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8specifications – Lumiscope 1100 User Manual

Page 8

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Specifications:

Measurement Method

: Oscillometric

Measurement Range

: Pressure: 20~280mmHg; Pulse: 40~180 beats/min

Pressure Sensor

: Semi conductor

Accuracy

: Pressure: ± 3mmHg; Pulse: ± 5% of reading

Inflation : Manual

Inflation

Deflation

: Automatic Pressure Release Valve

Memory capacity

: 60 memories

Auto-shut-off

: 1 minute after last button operation

Operating Environment

: Temperature: 5 °C ~ 45 °C (41 °F~113 °F); Humidity: 40 ~ 85%

Storage Environment

: Temperature: -10 °C ~ 60 °C (14 °F~140 °F );

Humidity: 10 ~ 95%

Power Source

: 3V DC, two ‘AA’ Batteries

Dimensions

: 115 (L) X 94.5 (W) X 60.5 (H) mm

Weight

: 320 g (G.W.) (No Batteries)

Arm circumference

: Adult: 24 ~36 cm (9.4”~14.2”) (standard)

*Specifications are subject to change without notice.

Cautionary Notes:

1. The unit contains high-precision assemblies. Therefore, avoid extreme temperatures,

humidity, and direct sunlight. Avoid dropping or strongly shocking the main unit, and protect it
from dust.

2. Clean the blood pressure monitor body and the cuff carefully with a slightly damp, soft cloth.

Do not iron, wash or use chemical cleaner on the cuff. Never use thinner, alcohol or petrol
(gasoline) as cleaner.

3. Leaky batteries can damage the unit. Remove the batteries when the unit will not used for a

long period of time.

4. The unit should not be operated by children.
5. If the unit is stored near freezing, allow it to acclimate at room temperature before use.
6. Your Lumiscope Blood Pressure Monitor is not field serviceable. You should not use any tool

to open the device nor should you attempt to adjust anything inside the device. If you have
any problems, please contact the store or the doctor from whom you purchased your
Lumiscope Blood Pressure Monitor.

7. For users diagnosed with common arrhythmia (atrial or ventricular premature beats or atrial

fibrillation), diabetes, poor circulation of blood, kidney problems, or for users who have
suffered a stroke, the device might not be suitable for use.

8. Do not use on unconcious patients.