HoMedics BPM83 Manual Del Usuario página 2

Intended Use
The BPM83 automatically measures adults' Systolic, Diastolic blood pressure and pulse rate by oscillometric method.
The measurement results are displayed on the LCD. Measurement position is at adult's upper arm. The intended use
of this over-the-counter device is for adults with upper arm circumference ranging from 220 mm to 420 mm (Approx.
8.7 ~ 16.6 inches) and for home use. When the device detects the appearance of irregular heartbeats such as atrial or
ventricular premature beats during measurement, an indicated symbol will appear with measuring readings.
This device is designed only for adults.
Type of Use/ Reuse
Multiple patient multiple use
Intended User
The Arm type blood pressure monitor is intended for both professional and consumer, and the patient is the intended
operator. Patient selection criteria: disabled persons are the exception: disabled persons need assistance by another
competent adult to use the device.
The CE marking with the Registration Number of
0598 the Notified Body. This denotes the compliance of
Regulation Medical Device Directive 93/42/EEC.
Medical Device
Manufacturer
Authorized representative in the European
Community
Date of manufacture
(YYYY-MM-DD or YYYY-MM)
Batch code LOT WWWXXXXX
LOT: Lot Number; WWW: working sheet; XXXXX:
serial no.
Serial number SN YYMWWWXXXXX
YY: year; M:month; WWW: working sheet; XXXXX:
serial no.
Keep dry
Temperature limit
Humidity limitation
Atmospheric pressure limitation
Caution
Consult the instruction for use
Disposal information: Should you wish to dispose
of the article, do so in accordance with current
regulations. Details are available from your local
authority.
WEEE 2012/19/EU Directives
This product fulfilling the requirements of the
RoHS
RoHS Directive 2011/65/EU.
INTRODUCTION
This product fulfilling the requirements of
the REACH Directive EC 1907/2006 and its
amendments, do not contain Substances of Very
REACH
High Concern in concentration above the limit of
0.1 %. No substance(s) is/are present in the parts
of the product above the concentration of 0.1 %
weight by weight.
Stand-by
Device classification type BF
This product meets the basic safety and essential
performance requirements indicated in the IP22
conditioning test (protection against solid foreign
objects of 12.5mm
vertically falling water drops when enclosure
tiled up to 15°)
The empty, completely flat batteries must
be disposed of through specially designated
collection boxes, recycling points or electronics
retailers. You are legally required to dispose of
the batteries.
Importer
Distributor
Model Number
Country of Manufacturer
Caution
Unique Device Identifier
2 I EN
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and greater and against