Specifications - Alvita MA801f Manual De Instrucciones

13. Dispose of device, batteries, components and accessories according to local
regulations.
14. This monitor may not meet its performance specification if stored or used
outside temperature and humidity ranges specified in Specifications.
Store between 10 – 90% RH
Store between 700 – 1060hPa

Specifications

Blood pressure measurements determined with MA801f are equivalent to those
obtained by a trained observer using cuff/stethoscope auscultation method, within
the limits prescribed by the American National Standard, Electronic or Automated
Sphygmomanometers. This unit is to be used by adult consumers in a home
environment. Do not use this device on infants or babies.
Measurement Method Oscillometric
Measurement Range Pressure: 30~260 mmHg; Pulse: 40~199 beats/ minute
Pressure Sensor Semi conductor
Accuracy Pressure: ± 3mmHg; Pulse: ± 5% of measurement
Inflation Pump Driven
Deflation Automatic Air Release Valve
Memory capacity 60 memories for each zone x 2 zones
Auto-shut-off 1 minute after last button operation
Operation Environment 10°C~40°C (50°F~104°F); 40%~85% RH; 700~1060 hPa
Storage and Transportation -10°C~60°C (14°F~140°F); 10%~90% RH; 700~1060 hPa
Environment
DC Power Source DC 6V four AA Batteries
Dimensions 160 (L) X 111 (W) X 75 (H) mm
Weight 310g (G.W.) (w/o Batteries)
Arm circumference Adult: 24~40 cm (9.4"~15.7")
14
m
90RH
10
n
1060hPa
700
Cuff materials Outer fabric: Nylon
Air bag: PVC
Tubing: PVC
Connector: ABS
Limited Users Adult users
Type BF: Device and cuff are designed to provide special protection
against electrical shocks.
IP Classification IP21: Protection against harmful ingress of water and particulate
matter
*Specifications are subject to change without notice.
This Blood Pressure Monitor complies with the European regulations and bears the CE mark "CE 0120".
The quality of the device has been verified and conforms to the provisions of the EC council directive
93/42/EEC (Medical Device Directive), Annex I essential requirements and applied harmonized standards.
EN 1060-1: 1995/A2: 2009 Non-invasive sphygmomanometers - Part 1 - General requirements
EN 1060-3: 1997/A2: 2009 Non-invasive sphygmomanometers - Part 3 - Supplementary requirements
for electro-mechanical blood pressure measuring systems
EN 1060-4: 2004 Non-invasive sphygmomanometers - Part 4: Test Procedures to determine the overall
system accuracy of automated non-invasive sphygmomanometers.
This blood pressure monitor was designed for long service time. To ensure accurate measurements, this
monitor is recommended to be re-calibrated every 2 years.
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