Specifications - Lumiscope 1146 Manual De Instrucciones

Tensiómetro digital de muñeca completamente automático
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Specifications

Model No.
Lumiscope 1146
Display
LCD Digital Display
Measuring Principle
Oscillometric Method
Measurable
13.5~21.5cm (5.3''~8.5'')
Circumference of Wrist
Electric Shock Protection
Internal power supply appliance type B
Backlight
White
Pressure
0 to 299 mmHg (0~39.9 kPa)
Measurement
Range
40 to180 Pulses/min
Pulse
Pressure
Accuracy
Pulse
3 Digits Display of mmHg or kPa
Pressure
LCD
Pulse
3 Digits Display
Indication
Symbol
Memory/IHB/Heartbeat/Low Battery,etc.
Specifications
The unit satisfies the requirements of IEC60601-1 Medical electrical equipment,
EN1060-1: Non-invasive sphygmomanometer, EN1060-3: Non-invasive
sphygmomanometer,IEC80601-2-30: Medical electrical equipment.
The unit satisfies the requirements of EN60601-1: Medical electrical equipment
Part 1: General requirements for basic safety and essential performance;
EN60601-1-2: Medical electrical equipment Part 1-2: General requirements for
basic safety and essential performance – Collateral standard: Electromagnetic
compatibility – Requirements and tests; EN1060-1:Non-invasive
sphygmomanometers – Part 1: General requirements; EN1060-3: Non-invasive
sphygmomanometers – Part 3: Supplementary requirements for
electro-mechanical blood pressure measuring system. EN1060-4: Non-invasive
sphygmomanometers – Part 4: Test procedures to determine the overall
system accuracy of automated non-invasive sphygmomanometers.
3 mmHg (0.4kPa)
5% of reading
33
35
Specifications
Inflation
Automatic by Internal Pump
Rapid Air Release
Automatic by Air Valve
Memory 180 (2*90) Sets of Measurement Values
Memory Function
Power Source
2 AAA Alkaline Batteries
Automatic Power-Off
In 2 Minutes
Gross Weight
Approx. 170g (Batteries not included)
Temperature
Operating
Environment
Humidity
Barometric Pressure
Storage
Temperature
Environment
Humidity
Specifications
The unit has passed the EMC Test.
Blood pressure measurements determined with this device are equivalent to
those obtained by a trained observer using the cuff/stethoscope auscultatory
method, within the limits prescribed by the American National Standard,
Manual, electronic, or automated sphygmomanometers.
The risk of patient and user can be lowered to an acceptable level.
Specifications are subject to change without notice due to improvements in
performance.
Applied parts include cuff.
The device, accessories, and packaging must be disposed of correctly at the
end of their usage. Please follow Local Ordinances and Regulations for
disposal.
Protection Class: Internally powered equipment
Applied Part Type: Type B
Moisture Protection: IPX0, continue operation
10 ~ 40 C (50 ~ 104 F)
15 ~ 90%RH (Noncondensing)
80~105 kPa
-20 ~ 60 C (-4 ~ 140 F)
10 ~ 95% RH (Noncondensing)
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