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Specifications:
Measurement Method : Oscillometric
Measurement Range : Pressure: 20~280mmHg; Pulse: 40~180 beats/ minute
Pressure Sensor : Semi conductor
Accuracy : Pressure: ± 3mmHg; Pulse: ± 5% of reading
Inflation : Pump Driven
Deflation : Automatic Pressure Release Valve
Memory capacity : 60-set memory
Auto-shut-off : 1 minute after last button operation
Operating Environment : Temperature: 10 °C ~ 40 °C (50 °F~104 °F); Humidity: 40 ~ 85%
Storage Environment : Temperature: -5 °C ~ 60 °C ( 23 °F~140 °F ); Humidity: 10 ~ 95%
Power Source : 6V DC four LR06 (AA) Batteries
Dimensions : 105 (L) X 160 (W) X 68 (H) mm
Weight : 360g(G.W.) (No Batteries)
Arm circumference : Adult: 22 ~32 cm (8.7”~12.6”) (standard)
: Large adult: 32 ~42 cm (12.6”~16.5”) (optional)
K.B. : Short time operation 2 minutes.
*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 or wash the cuff or use chemical cleaners on it.
Never use thinner, alcohol or petrol (gasoline) as a cleaner.
3. Leaky batteries can damage the unit. Remove the batteries when the unit is not used for a
long 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 1130 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 from which you purchased your model 1130 or contact the Lumiscope Repair
Department at 1-800-672-8293.
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 from stroke, the device might not be suitable for use.
8. Do not use on unconscious patients.
Manufactured by: The Lumiscope Co., Inc.