Compliance Information - Philips DL8791 User Manual

Prob lem Possible Solution
cause
Blood flow in Try loosening the
the skin can strap a notch to
be impacted relieve some pressure,
by increased but make sure the
pressure on watch still retains a
the small snug fit.
blood vessels
in the skin
(e.g. when the
watch strap is
too tight).
Blood flow in Disregard inaccurate
the skin can measures during
be temporarily warm-up exercises
reduced and provide some
during warm- time for the blood
up exercises flow to the skin
as more blood to adjust to the
is directed to exercising conditions.
the muscles.
Blood flow in Try wearing long-
the skin can sleeved clothing
be temporarily to cover the watch
reduced when and starting the
going outside measurement inside.
when it is Disregard inaccurate
very cold as measurements during
more blood is the first couple of
directed to the minutes and provide
body's core. some time for the
blood flow to the
skin to adjust to the
exercising conditions.
Transmittance Try re-positioning the
of light through watch at bit higher
the skin can up on the wrist or
be influenced on the other wrist
by stark (if you place the
contrast in watch on the other
pigmentation arm, do not forget
of the skin to change the watch
(e.g. due to a placement setting in
pattern in a the app).
tattoo). This
could result
in inaccurate
optical
heart rate
measurement.
Assistance
For assistance, visit our website:
www.philips.com/support or call toll free
1­844­531­6861
You can also visit the help section in the app.
Online information is available 24 hours a day,
7 days a week.
Full Two­Year Warranty
Philips Electronics North America Corporation
warrants each new Philips product, model DL8791,
against defects in materials or workmanship for a
period of two years from the date of purchase and
agrees to repair or replace any defective product
without charge.
IMPORTANT: This warranty does not cover damage
resulting from accident, misuse or abuse, lack of
reasonable care, the affixing of any attachment
not provided with the product or loss of parts or
subjecting the product to any but the specified
voltage.*
NO RESPONSIBILITY IS ASSUMED FOR ANY
SPECIAL, INCIDENTAL OR CONSEQUENTIAL
DAMAGES.
In order to obtain warranty service, simply go to
www.philips.com/support or call toll-free
1-844-531-6861. It is suggested that for your
protection you return shipments of product by
insured mail, insurance prepaid. Damage occurring
during shipment is not covered by this warranty.
NOTE: No other warranty, written or oral, is
authorized by Philips Electronics North America
Corporation. This warranty gives you specific
legal rights, and you may also have other rights
which vary from state to state. Some states do not
allow the exclusion or limitation of incidental or
consequential damages, so the above exclusion
and limitations may not apply to you.
* Read enclosed instructions carefully.
Manufactured for: Philips Consumer Lifestyle,
A division of Philips Electronics North America
Corporation, P.O. Box 10313, Stamford, CT 06904.
PHILIPS and Philips Shield are registered
trademarks of Koninklijke Philips N.V.
© 2016 Philips Electronics North America
Corporation. All Rights Reserved.

Compliance information

Electromagnetic emissions and immunity
The device is approved according to EMC safety
standard IEC 60601-1-2. It is designed to be used
in typical domestic environments.
Table 1 Guidance and manufacturer's
declaration – electromagnetic emissions
- for all ME equipment and ME systems
Guidance and manufacturer's declaration –
electromagnetic emissions
The device is intended for use in the
electromagnetic environment specified below.
The customer or the user of the device should
assure that it is used in such an environment.
Emissions Com­ Electromagnetic
test pli ance environment ­
guidance
RF emissions Group 1 The device must
CISPR 11 emit electromagnetic
energy in order to
perform its intended
function. Nearby
electronic equipment
may be affected.
RF emissions Class B The device is
CISPR 11 suitable for use in
all establishments,
Harmonic Not
including domestic
emissions IEC applica-
establishments
61000-3-2 ble
and those directly
connected to the
Voltage fluc tu- Not
public low voltage
a tions/flick er applica-
power supply
emissions IEC ble
network that supplies
61000-3-3
buildings used for
domestic purposes.
Declaration – electromagnetic immunity
Guidance and manufacturer's declaration –
electromagnetic immunity.
The device is intended for use in the
electromagnetic environment specified below.
The customer or the user of the device should
assure that it is used in such an environment.
IMMU­ IEC Com­ Electromagnetic
NI TY 60601 pli­ environment –
test test ance guidance
level level
Elec- ± 6 kV ± 6 kV Floors should be
tro sta- contact con- wood, concrete or
t ic dis- ± 8 kV tact ceramic tile. If floors
charge air ± 8 kV are covered with
(ESD) air synthetic material,
IEC the relative humidity
61000- should be at least
4-2 30 %.
Elec tri- ± 2 ± 2 Electrical power
cal fast kV for kV for quality should be
tran- power pow er that of a typical
sient/ supply sup- commercial
b urst lines ply or hospital
IEC ± 1 kV lines environment.
61000- for ± 1 kV
4-4 input/ for
out put inpu t/
Lines out put
Lines
Surge ± 1 kV ± 1 kV Electrical power
IEC line(s) line(s) quality should be
61000- to to that of a typical
4-5 line(s) line(s) commercial
± 2 kV or hospital
line(s) environment.
to earth
IMMU­ IEC Com­ Electromagnetic
NI TY 60601 pli­ environment –
test test ance guidance
level level
Voltage <5 % UT <5 % Electrical power
dips, (>95 % UT quality should be
short dip in (>95 that of a typical
inter- UT) % dip commercial
rup tions for 0,5 in UT) or hospital
and cycle for 0,5 environment. If the
voltage 40 % cycle user of the device
vari a- UT (60 40 % requires continued
tions on % dip in UT operation during
power UT) (60 power interruptions,
supply for 5 % dip it is recommended
input cycles in UT) that the device
lines IEC 70 % UT for 5 be powered from
61000- (30 % cycl es an uninterruptible
4-11 dip in 70 % power supply or a
UT) UT (30 battery.
for 25 % dip
cycles in UT)
<5 % UT
(>95 %
dip in
UT) for
5 s
Power 3 A/m 3A/m Power frequency
fre- magnetic fields
quen cy should be at levels
(50/60 characteristic of a
Hz) typical location in a
mag- typical commercial or
net ic hospital environment.
field IEC
61000-
4-8
Note: UT is the a.c. electrical voltage prior to
application of the test level.
Declaration – electromagnetic immunity
Guidance and manufacturer's declaration –
electromagnetic immunity.
The device is intended for use in the
electromagnetic environment specified below.
The customer or the user of the device should
assure that it is used in such an environment.
Immunity IEC 60601 test Compliance
test level level
Conducted 3 Vrms 150 kHz 3 Vrms
RF IEC to 80 Mhz
61000-4-6
Radiated RF 3 V/m 80 MHz 3 V/m
IEC 61000- to 2,5 Ghz
4-3
Note 1: At 80 MHz and 800 MHz, the higher
frequency range applies.