Contec CMS-50f User manual

After
setting
,
short
press
the button
to
select
“
Exit
”
，
then
long
press
the button
to
exit the
system
menu
and
return to
main
menu
.
5.3
.
5
Bluetooth
setting
Under
main
menu
,
short
press
the button
to
select
“
Bluetooth
”
，
then
long
press
the
button
to
enter
its
selection interface
as
shown
in
Figure
10
and
Figure
11
.
When
the Bluetooth is
“
ON
’
，
if
there is
no
data
to
be
transmitted
,
the Bluelooih will
turn
off
automatically
after
a
few
seconds
.
Note
:
under data
transmitting
state
by
Bluetooth
,
the Bluetooth
can
not
be turned off
.
Table
4
：
cathode
.
)
Guidance
and
manufacturer
'
s
declaration
-
electromagnetic
Immunity
Battery
life
Charge
and
discharge
:
no
less
than
500
times
Recycling garbage
WEEE
(
2012
/ 19 /
EU
)
The
[
Code
SI
]
is intended for
use
in
the
electromagnetic
environment
specified
below
.
The
customer
or the
USB
Output
voltage
: DC
5
V
Output
current
:
1000
mA
user
of the Pulse
Oximeter
should
assure
that
i
(
is used
in
such
an
environment
Adapter specification
I MM
UN
I
Test
Freque
Band Modul
alien b
)
TY
Dimensions and
Weight
Modulation Distance
Battery
anode
Battery
cathode
a
)
Service
a
)
TEST
LEVEL
(
V
/
m
)
Dimension
61
mm
(
L
)
>
：
56
mni
(
W
)
x
24 mm
(
H
)
b
)
(
m
)
ncy
(
MHz
)
(
W
)
(
MHz
)
Weight
About
60
g
(
including
a
lithium
battery
)
It
means
this
pulse
is
protected
against
harmful effects of
dripping
water
when tilled
at
15
°
.
Pulse
modulation
Turn
Off
81
?
Yes
E
3
Turn
On
BT
?
IP 22
RST RESET
hole
Yi
'
h
Q
380
Note
1
:
the claims of
SpC
>
2
accuracy
shall be
supported
by
clinical
study
measurements
taken
over
the full
range
.
By
artificial
inducing
,
get
the stable
oxygen
level
to
the
range
of
70
%
to
100
%
SpO
：
.
compare
the
Sp
( )
：
values collected
by
the
secondary
standard
pulse
oximeter
equipment
and the tested
equipment
al
the
used for
(
he
accuracy
analysis
.
(
li
is
applicable
for the
probes
385
TETRA
400
K
8 0
,
3
27
—
390
b
)
18
Hz
FMc
)
±
5
kHz
Humidity
limitation
Temperature
limitation
time
,
to
form
paired
data
,
which
430
GMRS
460
,
FRS
460
equipped
.
450
2
0
,
3 28
-
470
deviation
1 kHz
sine
II
There
are
12
healthy
volunteers
(
male
:
6
.
female
:
6
;
age
:
18
-
50
;
skin color
:
black
:
2
,
light
:
8
,
while
:
2
)
data
in
the clinical
report
.
Note
2
:
because
pulse
oximeter
equipment
measurements
are
statistically
distributed
,
only
about
hvo
-
thirds
of
pulse
oximeter
equipment
measurements
can be
expected
to
fall
within
土
Amis
of the value measured
by
a
CO
-
OXIMETER .
Figure
10
Bluetooth
“
ON
”
interface
Figure
11
Bluetooth
“
OFF
”
interface
Atmospheric
pressure
limitation
0
Radiated
This
way
up
5.3
.
6
Shutdown
Under
the
main
menu
interface
,
short
press
the button
to
select
“
Power
off
1
’
，
then
long
press
the button
to
turn
off
the device
.
710
Pulse
modulation
RF
704
LTE
Band
IEC
610
00
-
4
-
3
(
Test
sped
flea
tions for
ENCLO
SURE
PORT
1
MMUN
ITYto
745
02
0
,
3
9
r
-
787
13
,
17
b
)
5.3
.
7
E
\
il
main
menu
780
Under
main
menu
,
short
press
the button
to
select
“
Exit
”
，
then
long
press
the button
to
exit the
main
menu
and
return to
the
measurement
interface
.
5.4
Data
upload
5.4
.
1
Wired
transmission
Connect
the
device
to
computer
by
the
USB
cable
,
upload
the
data
after
connecting
with the
PC
software
properly
,
refer
to
“
Software
operating
instruction
”
for
details
.
Note
:
Ihe
PC
software
can
be downloaded from
our
official website
.
5.4
.
2
Bluetooth wired transmission
Turn
for d
5.5
Charging
Power
adapter
can
be selected
to
charge
for Ihe device
.
It
indicates
that
the device is
charging
when the indicator is
orange
,
the
charging
is
finished
when the
indicator
turns
to
green
.
5.6
Reset
Use
a
pointed
and hard
object
(
for
example
,
a
paper
clip
)
to
press
Ihe
reset
button inside of the
RESET
hole
,
to reset
the device
.
217
Hz
Note
3
:
Patient simulator has been used
to
verily
the
pulse
rate
accuracy
,
it
is stated
as
the
root
-
mean
-
square
difference between the
PR
measurement
value and the value
set
by
simulator
.
Note
4
:
percentage
modulation of infrared
signal
as
the indication of
pulsating signal strength
,
patieut
simulator has been used
to
verify
ils
accuracy
under conditions
of
low
perfusion
.
SpO
?
and
PR
values
are
different due
to
low
signal
conditions
,
compare
Ihcm with the known
SpO
:
and
PR
values of
input
signal
.
Note
5
:
optical
sensors as the
light
-
emitting
components
,
will
affect other medical devices
applied
the
wavelength
range
.
The
information
may
be useful for the
clinicians
who
carry
out
the
optical
treatment
.
For
example
,
photodynamic
therapy
operated
by
clinician
.
810
GSM
800
/
900
,
TETRA
870
Close
the sound
prompt
Pulse
modulation
800
800
,
2
0
,
3 28
b
)
O
iDEN
820
,
CDMA
850
,
LTE
Band
5
930
Open
the sound
prompt
Pause
Ihe sound
prompt
18
Hz
ou the device
Bluetooth
and
the
PC
software
to
upload
data
,
refer
to
“
Software
operating
instruction
'
d x
etails
.
0
-
山
Close
ihe
PR
sound
Menu
/
Power
button
RF
1720
GSM
1800
;
CDMA
1900
;
GSM
1900
;
DECT
;
LTE
Band
1
.
3
,
4
,
25
;
UMTS
wireless
1845
comm
u
n
ications
equipme
Pulse
Recyclable
Open
the
PR
sound
1700
modulation
2
0
,
3 28
b
)
-
1990
Prompt
condition
delay
Prompt
signal generation delay
State
1970
nt
)
Bluetooth icon
(
Bluetooth
wired device
)
217
Hz
Manufaclure Dale
Low
vo
I
tag
cprompt
20
ms
Is
6.1
Cleaning
and
Disinfecting
The device
must
be turned
off before
cleaning
,
and
it
should
not
be
immersed into
liquid
.
Please take
out
the
internal
battery
before
cleaning
,
do
not
immerse
it
into
liquid
.
Use
75
%
alcohol
to
wipe
the device enclosure
,
and
use
liquid
soap
or
isopropanol
to
wipe
the watchband
for
disinfection
,
nature
dry
or
clean
it
with clean and soft cloth
.
Do
noJ
spray any
liquid
on
the device
directly
,
and avoid
liquid
penetrating
into the device
.
6.2
IVIainlcnancc
A
.
Check
the
main
unit and
all
accessories
periodically
to
make
sure
that
there is no visible
damage
that
may
affect
user
’
s
safety
and
monitoring
performance
.
It
is
recommended
lhai
the device
should
be
inspected
weekly
at
least
.
When
there
is obvious
damage
,
stop
using
it
.
B
.
Please
clean and disinfect the
device be
fore
/
after
using
it
according
to
the
User
Manual
(
6.1
)
.
C
.
Plcasc
charge
the
battery
in
lime when low
battery
appears
.
D
.
Recharge
the
battery
soon after over
-
discharge
.
The device should be
recharged
every
three months when
it
is
not
used
for
some time
.
It
can extend the
battery
life
following
this
guidance
.
E
.
The device
need
not to
be
calibrated
during
maintenance
.
6.3
Transportation
and
Storage
A
.
The
packed
device
can
be
transported
by ordinary
conveyance
or
according
io
transport
contract
.
During
traiLsporlation
,
avoid
strong
shock
,
vibration and
splashing
with
rain
or snow
,
and
it
can not
be
material
.
B
.
The
packed
device should be stored
in
room
with
no
corrosive
gases
and
good
vcnlilation
.
Temperature
:
-
40
°
C
~
60
°
C
;
Humidity
:
<
95
SpO
:
prompt
330
ms
20
ms
Sensor
Off
The
probe
is disconnected
.
Finger
Out
The
finger
is
not
inserted
.
Bluetooth
,
WLAN
,
802.11
b
/
g
/
n
,
RFID
2450
,
LTE
Band
7
Pulse
rate
prompt
330
ms
20
ms
Pulse
modulation
Probe
error
prompt
16
ms
20
ms
Sensor
Fault
2400
-
2570
Recording
Probe failure
R
*
2450
2
0
,
3 28
b
)
217
Hz
Material
code
Batch
No
.
P
/
N
LOT
EMC
1
.
The
finger
clip
falls off
Pulse
modulation
5240
Tabic
1
:
WLAN
802.11
5100
5500
0
-
2
0
,
3
9
2
.
Probe
error
3
.
Signal inadequacy
indicator
Alarm
inhibit
Guidance
and
manufacturer
’
s declaration
-
electromagnetic
emission
-
5800
b
)
a
/
n
5785
The Pulse
Oximeter
is intended for
use
in
the
electromagnetic
environment
specified
below
.
The
purchaser
or
Ihe
user
of the device should
assure
that
it
is used
in
such environment
.
217
Hz
NOTE
If
necessary
to
achieve the
IMMUNITY
TEST
LEVEL
,
the distance between the
transmitting
antenna
and the
ME
EQUIPMENT
or
ME
SYSTEM
may
be reduced
to
I
pcnnitlcd
by
IEC
61000
-
4
-
3
.
Note
：
Your
device
may
not
contain
all
the
following
symbols
.
The
I m
test
distance is
sPo
2
Emission
test
Compliance
|
see
note
1
]
RF
emissions
C
1
SPR
11
Group
I
a
)
For
some
services
,
only
tlic
uplink frequencies
are
included
.
b
)
The carrier shall be modulated
using
a
50
%
duly
cycle
square
wave
signal
.
c
)
As
an
alternative
to
FM
modulation
,
50
%
pulse
modulation
at
18
Hz
may
be
used because while
it
does
not
rq
^
rcscnt
actual modulation
,
it
would be
worst
case
.
transported
mixed with toxic
,
harmful
,
Display
range
0
%
-
99
%
Table
2
:
Measured
range
0
%
~
100
%
Guidance
and manufacturer
’
s
dcclaratiou
-
clcctromagnctic immunity
70
%
-
100
%
:
士
2
%
;
The Pulse
Oximeter
is intended for
use
in
the
electromagnetic
environment
specified
below
.
The
purchaser
or
Ihe
user
of ihe Pulse
Oximclcr
should
assure
lhat
it
is used
in
such environment
.
Accuracy
|
see
note
2
]
The
MANUFACTURER
should consider
reducing
the minimum
separation
distance
,
based
on
RISK MANAGEMENT
,
and
using
higher
IMMUNITY
TEST LEVELS
that
reduced
LEVELS
shall
be ailculated
using
the
following
equation
:
0
%
-
69
%
:
unspecified
.
Trouble Possible
Reason
Solution
appropriate
for the are
1
.
The
finger
is
not
properly
positioned
.
2
.
The
finger
is
shaking
or
the user
is
moving
.
3
.
The device
is
not
used
in
environment
required
by
the
manual
.
4
.
Thc
device works
abnormally
.
Resolution
1
%
.
separation
distance
.
Minimum
separation
distances for
higher
IMMUNITY TEST
1
.
Please insert the
finger properly
and
again
.
2
.
Lcl the user
keep
calm
3
.
Please
use
the device
in
normal
Immunity
test
IEC
60601
test
level
Compliance
level
measure
PR
E
=
M
Electrostatic
discharge
(
ESD
)
IEC
61000
-
4
-
2
±
8
kV
contact
±
8
kV
contact
The values
can
not
be
displayed normally
or
stably
Display
range
30
bpm
250
bpra
d
土
15
k
V
air
土
15
kV
air
Where
P
is the maximum
power
in
W
,
d is Ihe minimum
separation
distance
in
ra
,
and
E
is the
IMMUNITY
TEST
LEVEL
in
V
/
m
.
Measured
range
30
bpm
~
250
bpm
Power
frequency
(
50
/
60
Hz
)
magnetic
field
IEC
61000
-
4
-
8
4
.
Please
contact
ihe after
-
sales
.
±
2
bpm
during
the
pulse
rate
range
of
30
bpm
99
bpm
and
±
2
%
during
the
pulse
rate
range
of
100
bpm
-
250
bpm
.
30
A
/
m
30
A
/
m
Accuracy
|
see
note
31
1
.
Low
battery
or the
battery
is
drained
away
.
2
.
The device works
abnormally
.
The device
can not
be
1
.
Please
charge
the
battery
.
2
.
Please
contact
the
after
-
sales
.
Resolution
turned
on
arning
Don
'
t
near
active
HFSURGICAL
EQUIPMENT
and the
KF
shielded
room
of
an
ME
SYSTEM
for
magnetic
resonance
imaging
,
where the
intensity
of
EM
DISTURBANCES
is
high
.
Use
of this
equipment
adjacent
to
or
stacked with other
equipment
should be avoided because
it
could result
in
improper operation
.
If
such
use
is
necessary
,
this
equipment
and the other
equipment
should be observed
to
verify
that
they
are
operating
normally
.
Use
of accessories
,
transducers and cables other
than
those
specified
or
provided
by
the
manufacturer of this
equipment
could result
in
increased
electromagnetic
emissions
or
decreased
electromagnetic immunity
of
this
equipment
and result
in
improper operation
.
”
Portable
RF
communications
equipment
(
including
peripherals
such
as
antenna
cables and
external
antennas
)
should
be used
no
closer
than
30
cm
(
12
inches
)
lo
any
part
of
the
device
including
cables
specified
by
Che
manufacturer
.
Otherwise
,
degradation
of Ihe
performance
of
this
equipment
could result
.
Active medical devices
are
subject
to
special
EMC
precautions
and
Ihey
must
be installed and
used
in
accordance
、
vilh these
guidelines
.
Table
3
:
Low
perfusion
0.4
%
:
1
.
The device
enters
into the
energy
saving
mode
.
2
.
Low
battery
.
I
.
Please
conlacl
(
he
after
-
sales
.
2
.
Please
charge
the
battery
3
.
Please
conlacl
(
lie after
-
sales
.
Guidance
and manufacturer
’
s
declaration
—
electromagnetic irmnunity
Accuracy
under low
perfusion
[
see
note
41
The
display
disappears
suddenly
.
The Pulse
Oximeter
is intended for
use
in
the
electromagnetic
environment
specified
below
.
The
customer
the
user of the Pulse
Oximeter
should assure
that
it
is used
in
such environment
.
PR
:
±
2
bpm
during
the
pulse
rate
range
of
30
bpm
-
99
bpm
and
士
2
%
during
the
pulse
rate
range
of
100
bpm
250
bpm
.
3
.
The device works
abnormally
.
The device
can
not
be
used for full time after
charge
.
1
.
The
battery
is
not
charged
fully
.
2
.
The device works
abnormally
.
1
.
Please
charge
the
battery
.
2
.
Please
contact
the
after
-
sales
.
IEC
60601
test
level
Compliance
level
Immunity
test
der normal and ambient
light
conditions
,
the
SpO
?
deviation
Light
interference
%
Radiated
RF
10
V
/
m
80
MHz
-
2.7
GHz
10
V
/
m
80
MHz
-
2.7
GHz
The
battery
can
not
be
full
charged
even after
10
hours
charging
lime
.
Continuous
bar
-
graph display
,
the
higher display
indicates the
stronger
pulse
.
IEC
61000
-
4
-
3
Pulse
Intensity
The
battery
works
abnormally
.
Please
contact
the after
-
sales
.
NOTE
1
Al
80
MHz
and
800
MHz
,
the
higher
frequency
range
applies
.
NOTE
2
These
guidelines
may
not
apply
in
all
situations
.
Electromagnetic propagation
is affected
by
absorption
and
reflection from
structures
,
objects
and
people
.
Upper
and
lower
limit
of
measured values
1
.
The device is
not
operated
according
lo
the manual
.
2
.
The device works
abnormally
.
1
.
Please
operate
the device
according
to
the manual
.
2
.
Please
contact
the after
-
sales
.
SpO
：
0
%
100
%
The data
can
not
be
stored
.
Field
strengths
from fixed
transmitters
,
such
as
base
stations for
radio
(
cellular / cordless
)
telephones
and land
mobile radios
,
amateur
radio
,
AM
and
FM
radio broadcast and
TV
broadcast
cannot
be
predicted
theoretically
with
accuracy
.
To
assess the
electromagnetic
em
ironment due
to
fixed
RF
transmitters
,
ail
electromagnetic
site
survey
should
be
considered
.
If
the
measured field
strength
in
the location
in
which
the Pulse
Oximeter
is used
exceeds the
applicable
RF
compliance
level
above
,
the Pulse
Oximeter
should be observed
to
verify
normal
operation
.
If
abnormal
performance
is observed
,
additional
measures
may
be
necessary
,
such
as
reorienting
or
relocating
the Pulse
Oximeter
.
h
Over
the
frequency
range
150
KHz
to
80
MHz
,
field
strengths
should
be
less
than
3
V
/
m
.
PR
0
bpm
-
254
bpm
a
A
Optical
sensor
|
see
note
51
Note
：
Red
light Wavelength
:
about
660
nm
,
optical
output
power
：
<
6.65
mW
When
the device is disturbed
,
(
he data measured
may
fluctuate
，
please
measure
repeatedly
or
in
another environment
to
ensure
its
accuracy
.
Symbols Meaning Symbols Meaning
Infrared
light Wavelength
:
about
905
nm
.
optical
oulput
power
:
<
6.75
mW
©
Up
to
99
group
of
data under
auto
mode
,
total
duration docs
not
exceed
72
hours
.
Up
to
24
-
liour
data under
manual mode
.
Caution
,
consult
accompanying
documents
PRbpm
Pulse
rate
(
bpm
)
Memory
Pulse
oxygen
saturation
(
%
)
Safety
class
Internally
powered equipment
,
type
BF
applied
pari
International Protection
1 P
22
i
Fully charged
Manufacturer
Working voltage
DC
3.6
V
-
4.2
V
Working
current
<
100
mA
A
rechargeable
lithium
battery
(
3.7
V
)
(
The red
battery
denotes anode
,
the black wire
on
the ba
on
the
denotes
Serial
mimhei
.
Use
-
by
date
wire
ncry
Power
supply
Bluetooth
Specification
Working
frequency
:
2402
MHz
2480
MHz
Modulation mode
:
GFSK
Transmitting
power
:-6
dBm
,
+
4
dBm
Receiving sensitivity
:
-
93
dBm

FCC Caution
§ 15.19 Labeling requirements.
This device complies with part 15 of the FCC Rules. Operation is subject to the following two
conditions: (1) This device may not cause harmful interference, and (2) this device must accept
any interference received, including interference that may cause undesired operation.
§ 15.21 Information to user.
Any Changes or modifications not expressly approved by the party responsible for compliance
could void the user's authority to operate the equipment.
§ 15.105 Information to the user.
Note: This equipment has been tested and found to comply with the limits for a Class B digital
device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable
protection against harmful interference in a residential installation. This equipment generates
uses and can radiate radio frequency energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to radio communications. However, there is no
guarantee that interference will not occur in a particular installation. If this equipment does cause
harmful interference to radio or television reception, which can be determined by turning the
equipment off and on, the user is encouraged to try to correct the interference by one or more of
the following measures:
-Reorient or relocate the receiving antenna.
-Increase the separation between the equipment and receiver.
-Connect the equipment into an outlet on a circuit different from that to which the receiver is
connected.
-Consult the dealer or an experienced radio/TV technician for help.
The device has been evaluated to meet general RF exposure requirement. The device can be used
in portable/mobile exposure condition without restriction