Contec CMS-50f Manual de usuario

After

setting

short

press

the

button

select

“

Exit

”

，

then

long

press

the

button

exit

the

system

and

return

main

5.3

Bluetooth

setting

Under

main

short

press

the

button

select

“

Bluetooth

”

，

then

long

press

the

button

enter

its

selection

interface

shown

Figure

and

Figure

When

the

Bluetooth

“

’

，

there

data

transmitted

the

Bluelooih

will

turn

off

automatically

after

few

seconds

Note

under

data

transmitting

state

Bluetooth

the

Bluetooth

can

not

turned

off

Table

：

cathode

)

Guidance

and

manufacturer

declaration

electromagnetic

Immunity

Battery

life

Charge

and

discharge

less

than

500

times

Recycling

garbage

WEEE

(

2012

)

The

[

Code

]

intended

for

use

the

electromagnetic

environment

specified

below

The

customer

the

USB

Output

voltage

Output

current

1000

user

the

Pulse

Oximeter

should

assure

that

(

used

such

environment

Adapter

specification

Test

Freque

Band

Modul

alien

)

Dimensions

and

Weight

Modulation

Distance

Battery

anode

Battery

cathode

)

Service

)

TEST

LEVEL

(

)

Dimension

(

)

：

mni

(

)

(

)

(

)

ncy

(

MHz

)

(

)

(

MHz

)

Weight

About

(

including

lithium

battery

)

means

this

pulse

protected

against

harmful

effects

dripping

water

when

tilled

Pulse

modulation

Turn

Off

Yes

Turn

RST

RESET

hole

380

Note

the

claims

SpC

accuracy

shall

supported

clinical

study

measurements

taken

over

the

full

range

artificial

inducing

get

the

stable

oxygen

level

the

range

100

SpO

：

compare

the

(

)

：

values

collected

the

secondary

standard

pulse

oximeter

equipment

and

the

tested

equipment

the

used

for

(

accuracy

analysis

(

applicable

for

the

probes

385

TETRA

400

—

390

)

FMc

)

kHz

Humidity

limitation

Temperature

limitation

time

form

paired

data

which

430

GMRS

460

FRS

460

equipped

450

470

deviation

kHz

sine

There

are

healthy

volunteers

(

male

female

;

age

;

skin

color

black

light

while

)

data

the

clinical

report

Note

because

pulse

oximeter

equipment

measurements

are

statistically

distributed

only

about

hvo

thirds

pulse

oximeter

equipment

measurements

can

expected

fall

within

土

Amis

the

value

measured

OXIMETER

Figure

Bluetooth

“

”

interface

Figure

Bluetooth

“

OFF

”

interface

Atmospheric

pressure

limitation

Radiated

This

way

5.3

Shutdown

Under

the

main

interface

short

press

the

button

select

“

Power

off

’

，

then

long

press

the

button

turn

off

the

device

710

Pulse

modulation

704

LTE

Band

IEC

610

(

Test

sped

flea

tions

for

ENCLO

SURE

PORT

MMUN

ITYto

745

787

)

5.3

main

780

Under

main

short

press

the

button

select

“

Exit

”

，

then

long

press

the

button

exit

the

main

and

return

the

measurement

interface

5.4

Data

upload

5.4

Wired

transmission

Connect

the

device

computer

the

USB

cable

upload

the

data

after

connecting

with

the

software

properly

refer

“

Software

operating

instruction

”

for

details

Note

Ihe

software

can

downloaded

from

our

official

website

5.4

Bluetooth

wired

transmission

Turn

for

5.5

Charging

Power

adapter

can

selected

charge

for

Ihe

device

indicates

that

the

device

charging

when

the

indicator

orange

the

charging

finished

when

the

indicator

turns

green

5.6

Reset

Use

pointed

and

hard

object

(

for

example

paper

clip

)

press

Ihe

reset

button

inside

the

RESET

hole

reset

the

device

217

Note

Patient

simulator

has

been

used

verily

the

pulse

rate

accuracy

stated

the

root

mean

square

difference

between

the

measurement

value

and

the

value

set

simulator

Note

percentage

modulation

infrared

signal

the

indication

pulsating

signal

strength

patieut

simulator

has

been

used

verify

ils

accuracy

under

conditions

low

perfusion

SpO

and

values

are

different

due

low

signal

conditions

compare

Ihcm

with

the

known

SpO

and

values

input

signal

Note

optical

sensors

the

light

emitting

components

will

affect

other

medical

devices

applied

the

wavelength

range

The

information

may

useful

for

the

clinicians

who

carry

out

the

optical

treatment

For

example

photodynamic

therapy

operated

clinician

810

GSM

800

900

TETRA

870

the

sound

prompt

Pulse

modulation

800

)

iDEN

820

CDMA

850

LTE

Band

930

Open

the

sound

prompt

Pause

Ihe

sound

prompt

the

device

Bluetooth

and

the

software

upload

data

refer

“

Software

operating

instruction

d x

etails

山

ihe

sound

Power

button

1720

GSM

1800

;

CDMA

1900

;

GSM

1900

;

DECT

;

LTE

Band

;

UMTS

wireless

1845

comm

ications

equipme

Pulse

Recyclable

Open

the

sound

1700

modulation

)

1990

Prompt

condition

delay

Prompt

signal

generation

delay

State

1970

)

Bluetooth

icon

(

Bluetooth

wired

device

)

217

Manufaclure

Dale

Low

tag

cprompt

6.1

Cleaning

and

Disinfecting

The

device

must

turned

off

before

cleaning

and

should

not

immersed

into

liquid

Please

take

out

the

internal

battery

before

cleaning

not

immerse

into

liquid

Use

alcohol

wipe

the

device

enclosure

and

use

liquid

soap

isopropanol

wipe

the

watchband

for

disinfection

nature

dry

clean

with

clean

and

soft

cloth

noJ

spray

any

liquid

the

device

directly

and

avoid

liquid

penetrating

into

the

device

6.2

IVIainlcnancc

Check

the

main

unit

and

all

accessories

periodically

make

sure

that

there

visible

damage

that

may

affect

user

’

safety

and

monitoring

performance

recommended

lhai

the

device

should

inspected

weekly

least

When

there

obvious

damage

stop

using

Please

clean

and

disinfect

the

device

fore

after

using

according

the

User

Manual

(

6.1

)

Plcasc

charge

the

battery

lime

when

low

battery

appears

Recharge

the

battery

soon

after

over

discharge

The

device

should

recharged

every

three

months

when

not

used

for

some

time

can

extend

the

battery

life

following

this

guidance

The

device

need

not

calibrated

during

maintenance

6.3

Transportation

and

Storage

The

packed

device

can

transported

ordinary

conveyance

according

transport

contract

During

traiLsporlation

avoid

strong

shock

vibration

and

splashing

with

rain

snow

and

can

not

material

The

packed

device

should

stored

room

with

corrosive

gases

and

good

vcnlilation

Temperature

;

Humidity

SpO

prompt

330

Sensor

Off

The

probe

disconnected

Finger

Out

The

finger

not

inserted

Bluetooth

WLAN

802.11

RFID

2450

LTE

Band

Pulse

rate

prompt

330

Pulse

modulation

Probe

error

prompt

Sensor

Fault

2400

2570

Recording

Probe

failure

2450

)

217

Material

code

Batch

LOT

EMC

The

finger

clip

falls

off

Pulse

modulation

5240

Tabic

WLAN

802.11

5100

5500

Probe

error

Signal

inadequacy

indicator

Alarm

inhibit

Guidance

and

manufacturer

’

declaration

electromagnetic

emission

5800

)

5785

The

Pulse

Oximeter

intended

for

use

the

electromagnetic

environment

specified

below

The

purchaser

Ihe

user

the

device

should

assure

that

used

such

environment

217

NOTE

necessary

achieve

the

IMMUNITY

TEST

LEVEL

the

distance

between

the

transmitting

antenna

and

the

EQUIPMENT

SYSTEM

may

reduced

pcnnitlcd

IEC

61000

Note

：

Your

device

may

not

contain

all

the

following

symbols

The

test

distance

sPo

Emission

test

Compliance

see

note

]

emissions

SPR

Group

)

For

some

services

only

tlic

uplink

frequencies

are

included

)

The

carrier

shall

modulated

using

duly

cycle

square

wave

signal

)

alternative

modulation

pulse

modulation

may

used

because

while

does

not

rcscnt

actual

modulation

would

worst

case

transported

mixed

with

toxic

harmful

Display

range

Table

Measured

range

100

Guidance

and

manufacturer

’

dcclaratiou

clcctromagnctic

immunity

100

士

;

The

Pulse

Oximeter

intended

for

use

the

electromagnetic

environment

specified

below

The

purchaser

Ihe

user

ihe

Pulse

Oximclcr

should

assure

lhat

used

such

environment

Accuracy

see

note

]

The

MANUFACTURER

should

consider

reducing

the

minimum

separation

distance

based

RISK

MANAGEMENT

and

using

higher

IMMUNITY

TEST

LEVELS

that

reduced

LEVELS

shall

ailculated

using

the

following

equation

unspecified

Trouble

Possible

Reason

Solution

appropriate

for

the

are

The

finger

not

properly

positioned

The

finger

shaking

the

user

moving

The

device

not

used

environment

required

the

manual

Thc

device

works

abnormally

Resolution

separation

distance

Minimum

separation

distances

for

higher

IMMUNITY

TEST

Please

insert

the

finger

properly

and

again

Lcl

the

user

keep

calm

Please

use

the

device

normal

Immunity

test

IEC

60601

test

level

Compliance

level

measure

Electrostatic

discharge

(

ESD

)

IEC

61000

contact

The

values

can

not

displayed

normally

stably

Display

range

bpm

250

bpra

土

air

土

air

Where

the

maximum

power

Ihe

minimum

separation

distance

and

the

IMMUNITY

TEST

LEVEL

Measured

range

bpm

250

bpm

Power

frequency

(

)

magnetic

field

IEC

61000

Please

contact

ihe

after

sales

bpm

during

the

pulse

rate

range

bpm

and

during

the

pulse

rate

range

100

bpm

250

bpm

Accuracy

see

note

Low

battery

the

battery

drained

away

The

device

works

abnormally

The

device

can

not

Please

charge

the

battery

Please

contact

the

after

sales

Resolution

turned

arning

Don

near

active

HFSURGICAL

EQUIPMENT

and

the

shielded

room

SYSTEM

for

magnetic

resonance

imaging

where

the

intensity

DISTURBANCES

high

Use

this

equipment

adjacent

stacked

with

other

equipment

should

avoided

because

could

result

improper

operation

such

use

necessary

this

equipment

and

the

other

equipment

should

observed

verify

that

they

are

operating

normally

Use

accessories

transducers

and

cables

other

than

those

specified

provided

the

manufacturer

this

equipment

could

result

increased

electromagnetic

emissions

decreased

electromagnetic

immunity

this

equipment

and

result

improper

operation

”

Portable

communications

equipment

(

including

peripherals

such

antenna

cables

and

external

antennas

)

should

used

closer

than

(

inches

)

any

part

the

device

including

cables

specified

Che

manufacturer

Otherwise

degradation

Ihe

performance

this

equipment

could

result

Active

medical

devices

are

subject

special

EMC

precautions

and

Ihey

must

installed

and

used

accordance

、

vilh

these

guidelines

Table

Low

perfusion

0.4

The

device

enters

into

the

energy

saving

mode

Low

battery

Please

conlacl

(

after

sales

Please

charge

the

battery

Please

conlacl

(

lie

after

sales

Guidance

and

manufacturer

’

declaration

—

electromagnetic

irmnunity

Accuracy

under

low

perfusion

[

see

note

The

display

disappears

suddenly

The

Pulse

Oximeter

intended

for

use

the

electromagnetic

environment

specified

below

The

customer

the

user

the

Pulse

Oximeter

should

assure

that

used

such

environment

bpm

during

the

pulse

rate

range

bpm

and

士

during

the

pulse

rate

range

100

bpm

250

bpm

The

device

works

abnormally

The

device

can

not

used

for

full

time

after

charge

The

battery

not

charged

fully

The

device

works

abnormally

Please

charge

the

battery

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

MHz

2.7

GHz

MHz

2.7

GHz

The

battery

can

not

full

charged

even

after

hours

charging

lime

Continuous

bar

graph

display

the

higher

display

indicates

the

stronger

pulse

IEC

61000

Pulse

Intensity

The

battery

works

abnormally

Please

contact

the

after

sales

NOTE

MHz

and

800

MHz

the

higher

frequency

range

applies

NOTE

These

guidelines

may

not

apply

all

situations

Electromagnetic

propagation

affected

absorption

and

reflection

from

structures

objects

and

people

Upper

and

lower

limit

measured

values

The

device

not

operated

according

the

manual

The

device

works

abnormally

Please

operate

the

device

according

the

manual

Please

contact

the

after

sales

SpO

：

100

The

data

can

not

stored

Field

strengths

from

fixed

transmitters

such

base

stations

for

radio

(

cellular

cordless

)

telephones

and

land

mobile

radios

amateur

radio

and

radio

broadcast

and

broadcast

cannot

predicted

theoretically

with

accuracy

assess

the

electromagnetic

ironment

due

fixed

transmitters

ail

electromagnetic

site

survey

should

considered

the

measured

field

strength

the

location

which

the

Pulse

Oximeter

used

exceeds

the

applicable

compliance

level

above

the

Pulse

Oximeter

should

observed

verify

normal

operation

abnormal

performance

observed

additional

measures

may

necessary

such

reorienting

relocating

the

Pulse

Oximeter

Over

the

frequency

range

150

KHz

MHz

field

strengths

should

less

than

bpm

254

bpm

Optical

sensor

see

note

Note

：

Red

light

Wavelength

about

660

optical

output

power

：

6.65

When

the

device

disturbed

(

data

measured

may

fluctuate

，

please

measure

repeatedly

another

environment

ensure

its

accuracy

Symbols

Meaning

Symbols

Meaning

Infrared

light

Wavelength

about

905

optical

oulput

power

6.75

group

data

under

auto

mode

total

duration

docs

not

exceed

hours

liour

data

under

manual

mode

Caution

consult

accompanying

documents

PRbpm

Pulse

rate

(

bpm

)

Memory

Pulse

oxygen

saturation

(

)

Safety

class

Internally

powered

equipment

type

applied

pari

International

Protection

Fully

charged

Manufacturer

Working

voltage

3.6

4.2

Working

current

100

rechargeable

lithium

battery

(

3.7

)

(

The

red

battery

denotes

anode

the

black

wire

the

denotes

Serial

mimhei

Use

date

wire

ncry

Power

supply

Bluetooth

Specification

Working

frequency

2402

MHz

2480

MHz

Modulation

mode

GFSK

Transmitting

power

:-6

dBm

Receiving

sensitivity

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

Otros manuales para CMS-50f

Otros manuales de Equipo médico de Contec

Contec

Contec CMS60C Manual de usuario

Contec

Contec CMS80A Manual de instrucciones

Contec

Contec CMS60D Manual de usuario

Contec

Contec CMS50QB Manual de instrucciones

Contec

Contec CMS60C Manual de usuario

Contec

Contec CMS 50IW Manual de usuario

Contec

Contec CMS50DL Manual de usuario

Contec

Contec CMS-50D Plus Manual de usuario

Contec

Contec CMS60C Manual de usuario

Contec

Contec ECG1200G Manual de usuario

Contec

Contec PM-60A Manual de usuario

Contec

Contec CMS50DA Manual de usuario

Contec

Contec CMS8000 Manual de usuario

Contec

Contec CMS-50f Manual de usuario

Contec

Contec CMS50EW Manual de usuario

Contec

Contec ESA0008 Manual de usuario

Contec

Contec CMS-50E Manual de usuario

Contec

Contec CMS50DL1 Manual de usuario

Contec

Contec CMS8000 Manual de usuario

Contec

Contec ABPM 50 Guía de referencia

Contec

Contec CMS50EW Manual de usuario

Contec

Contec CMS-50f Manual de usuario

Contec

Contec CMS-50f Manual de usuario

Contec

Contec CMS50DL Manual de usuario

Manuales populares de Equipo médico de otras marcas

TekTone

TekTone Tek-CARE160 Manual de usuario

NeuroMetrix

NeuroMetrix Quell 2.0 Manual de usuario

AMT

AMT XLR8 Manual de usuario

Medipost-Nutristoma

Medipost-Nutristoma MD300K2 Manual de usuario

EDAN

EDAN SONOTRAX Pro Manual de usuario

Restorative Therapies

Restorative Therapies RT300 Manual de usuario

Gendex

Gendex Expert DC Manual de usuario

Dexcowin

Dexcowin ADX4000W Manual de usuario

Libelium

Libelium MySignals Manual de usuario

Acelity

Acelity V.A.C.ULTA 4 Manual de usuario

Caputron

Caputron ActivaDose II tDCS Manual de usuario

FujiFilm

FujiFilm Sonart Manual del propietario

Plinth 2000

Plinth 2000 93CDT Manual de usuario

GE SENOGRAPHE 800T Manual de usuario

GE Definium 5000 Manual de usuario

Kanmed

Kanmed GE-1380 Manual de usuario

Huntleigh

Huntleigh FD1 Manual de usuario

Stryker

Stryker SPR Plus Manual de usuario