Speci Cations - Omron M7 Intelli IT Manual De Instrucciones

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