Owner's Manual
Arm-type Fully Automatic
Digital Blood Pressure Monitor
DBP-6179
Model
Arm Type
Arm Type
Contents
Safety Notice ...............................................................
Quick Start ................................................................. 10
Unit Operation ...........................................................
Testing ................................................................ 15
Power Off .............................................................17
Memory Check and Last 3 Test Average
Maintenance ............................................................... 26
Specifications ............................................................. 28
Warranty .................................................................... 30
...................................................
0123
EC
1
Safety Notice
Thank you for purchasing the DBP-6179 Blood Pressure Monitor. The unit has been
02
constructed using reliable circuitry and durable materials. Used properly, this unit will
provide yeas of satisfactory use.
06
The digital blood pressure monitor is intended for measurement the systolic and diastolic
blood pressureand pulse rate from upper-arm of adults and adolescents over the age of 12
by using a non-invasive technique. The device can be reusable for clinical use and home use.
All functions can be used safely and values can also be read out on the LCD DISPLAY.
The measurement position is placed only on the upper-arm of an adult. This PATIENT is an
intended OPERATOR.
Please read this manual thoroughly before using the unit. Please retain this manual for
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future reference. For specific information about your blood pressure, please
CONSULT YOUR DOCTOR.
To avoid risk and damage follow all warning precautions. Operate unit only as intended.
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Read all instructions prior to use.
WARNING SIGNS AND SYMBOLS USED
.............18
SN
0123
EC
REP
MD
36
Date of Issue: 2020.06
Importer
The product is in compliance with the requirements of the Regulation
(EU) 2017/745 MDR on medical device, "0123" is the identification
number of notify body
JOYTECH Healthcare Co., Ltd.
No.365, Wuzhou Road, 311100 Hangzhou, Zhejiang Province,
PEOPLE'S REPUBLIC OF CHINA
Shanghai International Holding Corp. GmbH (Europe)
REP
Eiffestrasse 80, 20537 Hamburg, Germany
Caution
Mandatory
Prohibited
Type BF Equipment
Instructions For Use MUST be Consulted
Serial Number
Discard the used product to the recycling collection
point according to local regulations
The product conforms to the requirements of the
Regulation (EU) 2017/745 MDR on medical devices
Manufacturer
Authorised Representative in the European Community
Keep Dry
Keep off Sunlight
Manufacturing Date
Medical Device
Represents transport and storage temperature limits
Represents transport and storage humidity limits
Document No. : JDBP-7904-002
Version: Z
2
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