Owner's Manual
Arm-type Fully Automatic
Digital Blood Pressure Monitor
Model
Contents
Safety Notice ...............................................................
Quick Start ................................................................. 10
Unit Operation ...........................................................
Testing ..................................................................... 15
Power Off ................................................................
Memory Check ........................................................
&
Maintenance ............................................................... 28
Specifications ............................................................. 30
Warranty .................................................................... 32
........................................................ 37
DBP-1383
0123
EC
REP
1
Safety Notice
Thank you for purchasing the DBP-13
using reliable circuitry and durable materials. Used properly, this unit will provide yeas of
02
satisfactory use.
06
Intended use: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.
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Please read this manual thoroughly before using the unit. Please retain this manual for
future reference. For specific information about your blood pressure, please
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CONSULT YOUR DOCTOR.
To avoid risk and damage follow all warning precautions. Operate unit only as intended.
12
Read all instructions prior to use.
WARNING SIGNS AND SYMBOLS USED
Caution
Mandatory
18
Prohibited
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Type BF Equipment
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Instructions For Use MUST be Consulted
SN
Serial Number
22
Discard the used product to the recycling
collection point according to local
regulations
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The product conforms to the requirements of the
Regulation (EU) 2017/745 MDR on medical devices
0123
Manufacturer
Authorised Representative in the European Community
EC
REP
Keep Dry
Keep off Sunlight
Manufacturing Date
MD
Medical Device
Document No.:JDBP-8304-002
Version: B
Date of Issue:2020.09.26
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)
Eiffestrasse 80, 20537 Hamburg, Germany
83
Blood Pressure Monitor. The unit has been constructed
The PATIENT is an intended OPERATOR.
2
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