Symbol for “THE OPERATION
GUIDE MUST BE READ”
Symbol for “TYPE BF APPLIED
PARTS”
Symbol for “MANUFACTURER”
Symbol for “ENVIRONMENT
PROTECTION - Electrical waste
products should not be disposed of
with household waste. Please
recycle where facilities exist. Check
with your local authority or retailer
for recycling advice”
Symbol for “SERIAL NUMBER”
Symbol for “DIRECT CURRENT”
Symbol for “RECYCLE”
Symbol for “MANUFACTURE DATE”
Caution: These notes must be
observed to prevent any damage
to the device.
SN
INTRODUCTION
INTRODUCTION
General Description
Measurement Principle
Safety Information
Indications for Use
Contraindications
Thank you for selecting the Pylo PY-802-LTE arm type blood pressure monitor.
The monitor features blood pressure measurement, pulse rate measurement and digital result
storage. Readings taken by the PY-802-LTE are equivalent to those obtained by a trained observer
using the cuff and stethoscope auscultation method. This manual contains important safety and
care information, and provides step by step instructions for using the product.
Please read this manual thoroughly before using the product.
This product uses the Oscillometric Measuring Method to detect blood pressure.
Before every measurement, the unit establishes a “zero point” equivalent to the atmospheric
pressure prior to inflating the cuff. Meanwhile, the unit detects pressure oscillation generated by
beat-to-beat pulsatile, which is used to determine the systolic pressure and diastolic pressure as
well as pulse rate.
The signs below might be in the user manual, labeling or other components.
They are the requirement of standard and using.
Features:
• 78*92mm Digital LCD display
• Measuring during inflation technology
• LTE-M wireless communication
The Pylo PY-802-LTE is a digital blood pressure monitor intended for use in measuring blood
pressure and heartbeat rate on users with an arm circumference ranging from 22cm to 42cm
(about 8¾˝-16½˝).
It is intended for adult indoor use only.
1.The device should not be used by any person who is suspected to be or is pregnant .
2.The device is not suitable for use on patients with implanted electrical devices such as cardiac
pacemakers or defibrillators.
3
2
