Owner's Manual
Table Of Contents
- Installation and Operating Instructions
- Minimum requirements
- Withings Thermo description
- Setting up my Withings Thermo
- Customizing the settings of the Withings Thermo
- Using my Withings Thermo
- Using the Withings Thermo app
- Getting personalized advice
- Dissociating my Withings Thermo
- Cleaning and maintenance
- Specifications
- Document release overview
- Warranty
- Regulatory statements
- Quick Installation Guide
- Regulatory information
Disposal
Actuation
of
European directives
2002/95/EC
,
2002/96/EC
and
2003/108/EC
,
for
reduction in use
of
dangerous
substances
in
the
electric
and
electronic
device
and
for
garbage
disposal.
The symbol
applied
on
the
device
or
its packaging means
that
at
the
end
of
its useful life
the
product
must
not
be
disposed
of
with
domestic
waste.
At
the
end
of
devices useful life,
the
user
must
deliver
it
to
the
able
collecting
centers
for
electric
and
electronic
garbage,
or
give
back
to
the
retailer when purchasing
a
new
device. Disposing
of
the
product
separately prevents
possible negative consequences
for
the
environment
and
for
health, deriving from inadequate disposal. It also allows the
recovery
of
materials
of
which it's
made
up
in
order
to
obtain
an
important
saving
of
energy
and
resources and
to
avoid
negative effects
to
the
environment and health.
In
case
of
abusive
disposal
of
device
by
the
user, will
be
applied
administrative
endorsements in
compliance
with
current standard. The device
and
its parts is
marred
with
regard
to
disposal,
as
appropriate,
in
accordance
with
national
or
regional regulations.
Reference
to
standards
This
device
complies
with
the
following
normative
documents:
COUNCIL DIRECTIVE
93/42/
EEC
of
14
June
1993
concerning
medical
devices as
amended
by
Directive
2007
1
47/EC.
EN
ISO 80601-2-56: Particular
requirements
for basic safety
and
essential
performance
of
clinical
thermometers
for
body
temperature
measurement.
EN
ISO
12470
-5: "Clinical ther-
mometers"
• Part 5: Performance
of
infrared
thermometers
(with
maximum
device).
ASTM
E
1965
: ASTM Standard for Infrared Cl:nical
Thermometer.
This infrared
thermometer
meets
requirements established ;n ASTM Standard (E 1965-98). Full responsibility
for
the
confor-
mance
of
this
product
to
the
standard
is assumed
by
YA HORNG ELECTRONIC CO.,
LTD.
&
ATTEN ELECTRONIC
(DONGGUAN)
CO., LTD
188
industrial district, Ping Shan
Administra-
tive District, Tang Shia Town,
Dongguan,
Guangdong,
China.
EN
ISO 13485:
Medical
de
vices -
Ouality
management
systems - Requirements for regulatory
purposes
- Reference
to
standards contd. EN ISO14971:
Medical
devices -
Application
of
risk
management
to
medical devices. IEC/EN 60601-1:
Medical
electrical
equipment
- Part
1:
General requi-
rements for basic safety
and
essential
performance
IEC/EN 60601-1 -2:
Medical
electrical
equipment:
Part 1: General
requirements
for
basic safety
and
essential
performance
- col-
lateral standard
electromagnetic
compatibility. IEC/EN 60601-1-11 : General
requirements
for
basic safety
and
essential per-
formance
- Collateral Standard: Requirements
for
medi-
cal electrical
equipment
and
medical
electrical systems used
in
the
home
healthcare en-
vironment. EN300328
Electromagnetic
compatibility
and
Radio
spectrum
Matters (ERM);
Wideband
transmission systems;
Data
transmission
equipment
operating
in
the
2,4 GHz ISM
band
and
using
wide
band
modulation
techniques;
Harmonized
EN
covering
the
essential
requirements
of
article 3.2
of
the
Directive
2014/53/EU.
EN301489-1 Electromagnetic
com-
patibility
and
Radio
spectrum
Matters (ERM); Electr0Magnet1c
Compatibility
(EMC) standard
for
radio
equipment
and
services; Part
1:
Common
technical requirements. EN301489-17
Electromagnetic
compatibility
and
Radio
spectrum
Matters (ERM); ElectroMagnetic
Compa-
t1bt!1ty
(EMC) standard
for
radio
equipment
and
services; Part 1:
Common
technical require-
ments. EN 55011: Industrial, scientific
and
medical
equipment-Radiofrequency
disturbance
characteristics - Limits
and
methods
of
measurement. FCC part B
158
:
Electromagnetic
Compatibility.
FCC
Rule
Part
:
15.247
Cat: DSS
(Bluetooth)
FCC Rule Part: 15.247 Cat:
DTS
(B14.0). EN ISO
10993
-1:
Biological
evaluation
of
medical
devices - Part
1:
Evaluation
and
testing
within
a risk
management
process.
EN
ISO
10993
-5: Biological evaluation
of
medical
devices - Part 5: Tests
for
in
vitro cytotoxicity. EN ISO
10993
-10: Biological evaluation
of
medical devices -
Tests
for irritation
and
skin sensit1zat1on. EN ISO
1522
3-1:
Medical
devices
- Symbols
to
be
used
with
medical
device
labels,
labelling
and
information
to
be
supplied
.
Part 1: General requirements.