Speci Cations - Omron M7 Intelli IT Manual De Instrucciones

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6. Speci cations

Product Category
Electronic Sphygmomanometers
Product description
Automatic Upper Arm Blood Pressure
Monitor
Model (Code)
M7 Intelli IT (HEM-7361T-EBK) /
X7 Smart (HEM-7361T-ESL)
Display
LCD digital display
Cuff pressure range
0 to 299 mmHg
Blood pressure
SYS: 60 to 260 mmHg
measurement range
DIA: 40 to 215 mmHg
Pulse measurement range 40 to 180 beats / min.
Accuracy
Pressure: ±3 mmHg
Pulse: ±5% of display reading
Inflation
Automatic by electric pump
Deflation
Automatic pressure release valve
Measurement method
Oscillometric method
Bluetooth
Transmission method
Wireless communication Frequency range: 2.4 GHz (2400 -
2483.5 MHz) / Modulation: GFSK
Effective radiated power: < 20 dBm
Operation mode
Continuous operation
IP classification
Monitor: IP20
Optional AC adapter: IP21
Rating
DC6 V 4.0 W
Power source
4 "AA" batteries 1.5 V or optional
AC adapter (INPUT AC 100 - 240 V
50/60 Hz 0.12 - 0.065 A)
®
Low Energy
Battery life
Approximately 1000 measurements
(using new alkaline batteries)
The number of times may decrease when
using Afib mode because one Afib indication
consists of 3 regular measurements.
Durable period (Service
Monitor: 5 years / Cuff: 5 years /
life)
Optional AC adapter: 5 years
Operating conditions
+10 to +40°C / 15 to 90% RH
(non-condensing) / 800 to 1060 hPa
Storage / Transport
-20 to +60°C / 10 to 90% RH
conditions
(non-condensing)
Weight
Monitor: approximately 460 g
(not including batteries)
Arm cuff: approximately 163 g
Dimensions
Monitor: 191 mm (W) × 85 mm (H) ×
(approximately value)
120 mm (L) / Arm cuff:145 mm ×
532 mm (air tube: 750 mm)
Cuff circumference
220 to 420 mm
applicable to the monitor
Memory
Stores up to 100 readings per user
Contents
Monitor, arm cuff (HEM-FL31), 4 "AA"
batteries, Instruction Manual
Protection against
Internally powered ME equipment
electric shock
(When using only batteries)
Class II ME equipment (Optional AC
adapter)
Applied part
Type BF (arm cuff )
Note
• These specifications are subject to change without notice.
• This monitor is clinically investigated according to the requirements of
ISO 81060-2:2013. In the clinical validation study, K5 was used on 85 subjects
for determination of diastolic blood pressure.
• This device has been validated for use on pregnant and pre-eclampsia patients
according to the Modified European Society of Hypertension Protocol*.
• This device has been validated for use on diabetic (Type II) population**.
and
, setup instructions, storage case
EN
EN8

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Este manual también es adecuado para:

X7 smartHem-7361t-ebkHem-7361t-esl

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