background image

 

________________________________________________________________________________________________________________________________

 

TensioMed®

 

TensioDay

 

Plus™

 

19

 

 

Electromagnetic

 

immunity

 

The

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device

 

is

 

intended

 

for

 

use

 

in

 

the

 

electromagnetic

 

environment

 

specified

 

below.

 

The

 

customer

 

or

 

the

 

user

 

of

 

the

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device

 

should

 

assure

 

that

 

it

 

is

 

used

 

in

 

such

 

an

 

environment.

 

Immunity

 

test

 

IEC

 

60601

 

test

 

level

 

Compliance

 

level

Electromagnetic

 

environment

 

 

guidance

 

 

 

Portable

 

and

 

mobile

 

RF

 

communications

 

equipment

 

should

 

be

 

used

 

no

 

closer

 

to

 

any

 

part

 

of

 

the

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device,

 

including

 

cables,

 

than

 

the

 

recommended

 

separation

 

distance

 

calculated

 

from

 

the

 

equation

 

applicable

 

to

 

the

 

frequency

 

of

 

the

 

transmitter.

 

 

Recommended

 

separation

 

distance

 

 

d=1,2

P

 

 
 

d=1,2

P

 

80

 

MHz

 

 

800

 

MHz

 

d=2,3

P

 

800

 

MHz

 

 

2,5

 

GHz

 

 

where

 

P

 

is

 

the

 

maximum

 

output

 

power

 

rating

 

of

 

the

 

transmitter

 

in

 

watts

 

(W)

 

according

 

to

 

the

 

transmitter

 

manufacturer

 

and

 

d

 

is

 

the

 

recommended

 

separation

 

distance

 

in

 

metres

 

(m).

 

Field

 

strengths

 

from

 

fixed

 

RF

 

transmitters,

 

as

 

determined

 

by

 

an

 

electromagnetic

 

site

 

survey,

a

 

should

 

be

 

less

 

than

 

the

 

compliance

 

level

 

in

 

each

 

frequency

 

range.

b

 

Interference

 

may

 

occur

 

in

 

the

 

vicinity

 

of

 

equipment

 

marked

 

with

 

the

 

following

 

symbol:

 

 

Conducted

 

RF

  

IEC

 

61000

4

6

 

3

 

V

eff

 

150

 

kHz

 

 

80

 

MHz

 

 

3

 

V

 

 

Radiated

 

RF

 

IEC

 

61000

4

3

 

3

 

V/m

 

80

 

MHz

 

 

2,5

 

GHz

 

3

 

V/m

NOTE

 

1

   

At

 

80

 

MHz

 

and

 

800

 

MHz,

 

the

 

higher

 

frequency

 

range

 

applies.

NOTE

 

2

   

These

 

guidelines

 

do

 

not

 

apply

 

in

 

all

 

situations.

 

Electromagnetic

 

propagation

 

is

 

affected

 

by

 

absorption

 

and

 

reflection

 

from

 

structures,

 

objects

 

and

 

people.

 

a

 

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

 

environment

 

due

 

to

 

fixed

 

RF

 

transmitters,

 

an

 

electromagnetic

 

site

 

survey

 

should

 

be

 

considered.

 

If

 

the

 

measured

 

field

 

strength

 

in

 

the

 

location

 

in

 

which

 

the

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device

 

is

 

used

 

exceeds

 

the

 

applicable

 

RF

 

compliance

 

level

 

above,

 

the

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device

 

should

 

be

 

observed

 

to

 

verify

 

normal

 

operation.

 

If

 

abnormal

 

performance

 

is

 

observed,

 

additional

 

measures

 

may

 

be

 

necessary,

 

such

 

as

 

re

orienting

 

or

 

relocating

 

the

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device.

 

b

 

Over

 

the

 

frequency

 

range

 

150

 

kHz

 

to

 

80

 

MHz,

 

field

 

strengths

 

should

 

be

 

less

 

than

 

3

 

V/m.

 

 

Recommended

 

separation

 

distances

 

between

 

portable

 

and

 

mobile

 

RF

 

communications

 

equipment

 

and

 

the

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device

 

The

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device

 

is

 

intended

 

for

 

use

 

in

 

an

 

electromagnetic

 

environment

 

in

 

which

 

radiated

 

RF

 

disturbances

 

are

 

controlled.

 

The

 

customer

 

or

 

the

 

user

 

of

 

the

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device

 

can

 

help

 

prevent

 

electromagnetic

 

interference

 

by

 

maintaining

 

a

 

minimum

 

distance

 

between

 

portable

 

and

 

mobile

 

RF

 

communications

 

equipment

 

(transmitters)

 

and

 

the

 

TensioMed®

 

TensioDay

 

Plus™

 

TD3

 

device

 

as

 

recommended

 

below,

 

according

 

to

 

the

 

maximum

 

output

 

power

 

of

 

the

 

communications

 

equipment.

 

Rated

 

maximum

 

output

 

power

 

of

 

transmitter

 

W

 

Separation

 

distance

 

according

 

to

 

frequency

 

of

 

transmitter

 

m

 

150

 

kHz

 

 

80

 

MHz

 

d=[3,5/3]

P

 

80

 

MHz

 

 

800

 

MHz

 

d=[3,5/3]

P

 

800

 

MHz

 

 

2,5

 

GHz

 

d=[7/3]

P

 

0,01

 

0,12

 

0,12

0,23

 

0,1

 

0,38

 

0,38

0,73

 

1

 

1,2

 

1,2

2,3

 

10

 

3,8

 

3,8

7,3

 

100

 

12

 

12

23

 

For

 

transmitters

 

rated

 

at

 

a

 

maximum

 

output

 

power

 

not

 

listed

 

above,

 

the

 

recommended

 

separation

 

distance

 

d

 

in

 

metres

 

(m)

 

can

 

be

 

estimated

 

using

 

the

 

equation

 

applicable

 

to

 

the

 

frequency

 

of

 

the

 

transmitter,

 

where

 

P

 

is

 

the

 

maximum

 

output

 

power

 

rating

 

of

 

the

 

transmitter

 

in

 

watts

 

(W)

 

according

 

to

 

the

 

transmitter

 

manufacturer.

 

NOTE

 

1

 

At

 

80

 

MHz

 

and

 

800

 

MHz,

 

the

 

separation

 

distance

 

for

 

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.

 

 
 

Содержание tensioday plus

Страница 1: ...blood pressure monitor featuring central blood pressure measurement With wireless communication Bluetooth Please read the user s manual carefully before the first use TensioMed TensioDay Plus 5 02 v2...

Страница 2: ...________________________________________________________________________________________________________________________________ TensioMed TensioDay Plus 2...

Страница 3: ...s device 8 2 1 Explanation of symbols 8 2 2 Accessories 10 2 3 Installing the Device 10 2 4 Operations Instructions 11 2 4 1 Functions of the button on the device 12 2 4 1 1 One short push of the butt...

Страница 4: ...lood pressure readings are loaded via bluetooth communication from and to the physician s PC respectively Automatic measurements can be set for up to 48 hours with frequencies ranging from 10 to 90 mi...

Страница 5: ...company and product names mentioned herein may be trademarks of their respective companies 1 1 Contents of the manual This manual helps you in setting up and starting to use the TensioMed TensioDay Pl...

Страница 6: ...1182 Hungary Phone 36 1 433 1700 433 1701 Fax 36 1 433 1709 Web www tensiomed com E mail info tensiomed com 1 4 General Information warnings and precautions We strongly suggest that you carefully stud...

Страница 7: ...unit with special care Children should not use the device on their own Do not remove the outer cover of the device The TensioMed TensioDay Plus 24 hour BPM device is sophisticated multipurpose softwar...

Страница 8: ...flation continues above this value or the pressurization lasts too long unplug the pneumatic connector of the cuff from the device and remove the cuff from the subject Do not use the device on an arm...

Страница 9: ...anual 12 Certification mark guaranteeing that the apparatus complies with the prescriptions and requirements of the European Union 13 Serial number 14 Operating ambient temperature range 15 Year of th...

Страница 10: ...ircumference range Cuff S 20 8 cm 41 5 10 cm 20 24 cm Cuff M 23 11 5 cm 57 14 cm 24 32 cm Cuff L 28 x 11 5 cm 64 x 14 cm 32 38 cm The manufacturer of the cuffs ERKA Kallmeyer Medizintechnik GmbH Co KG...

Страница 11: ...ay The batteries and charging appliances have their own Instructions for use we suggest you study them and follow manufacturers guidelines In case you do not have a Bluetooth communication adapter or...

Страница 12: ...Day Plus is ready for operation D 09 39 2 4 1 1 One short push of the button starts a manual measurement During the ambulatory measuring mode there might be a need for manual measurements for example...

Страница 13: ...s ready for measurement for manual and programmed mode OFF 2 4 1 2 Two short pushes on the button Pill allows the patient to keep his electronic diary concerning taking his antihypertensive medication...

Страница 14: ...nloads all the stored data to the physician s PC via Bluetooth communication The information loaded consists of the systolic and diastolic blood pressure values mmHg the pulse rate per minute the dist...

Страница 15: ...the patient s blood pressure within the measuring time 3 The measurement was interrupted due to the weakness of the battery 31 The cuff is not connected to the device 32 The cuff tube is broken or so...

Страница 16: ...ree ambulation to avoid skin irritation a thin shirt might be used below the cuff the tube of the cuff should be inserted into the air connector of the device see figure 1 Attention Please take care o...

Страница 17: ...asurement method Oscillometric Data Storage Max 1000 measurements Blood Pressure measurements range 30 280 mmHg Static accuracy 3 mmHg or 2 of the measured value Measuring accuracy Systolic 94 out of...

Страница 18: ...ice is intended for use in the electromagnetic environment specified below The customer or the user of the TensioMed TensioDay Plus TD3 device should assure that it is used in such an environment Immu...

Страница 19: ...the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the TensioMed TensioDay Plus TD...

Страница 20: ...________________________________________________________________________________________________________________________________ TensioMed TensioDay Plus 20...

Страница 21: ...________________________________________________________________________________________________________________________________ TensioMed TensioDay Plus 21...

Страница 22: ...________________________________________________________________________________________________________________________________ TensioMed TensioDay Plus 22...

Страница 23: ...________________________________________________________________________________________________________________________________ TensioMed TensioDay Plus 23...

Страница 24: ...________________________________________________________________________________________________________________________________ TensioMed TensioDay Plus 24...

Отзывы: