Keeler Pulsair Desktop Instructions For Use Manual

Download

Instructions for use

Back

Contents

1. Copyright and Trademarks .............................................p3

Introduction ....................................................................p4

Symbols ...........................................................................p5

Safety ...............................................................................p6

4.1 Device Classification .................................................p6

4.2 Warnings and cautions ............................................p6

Cleaning instructions ......................................................p7

Power supply assembly ..................................................p8

Mounting ........................................................................p9

Tonometry pressure variations in the human eye ......p10

Names of controls and components ...........................p11

10.

Measurement procedures ............................................p16

10.1 Preparing the device ............................................p16

10.2 Preparing the patient ...........................................p17

10.3 Taking the reading ...............................................p18

11.

Display examples ..........................................................p19

12.

Printing ..........................................................................p20

13.

Replacing the printer paper ........................................p21

14.

User menu options .......................................................p22

15.

Calibration, maintenance and inspection ...................p23

16.

Specifications and electrical ratings ............................p25

17.

Accessories and warranty .............................................p31

18.

Contact, packaging and disposal information ...........p32

Please click on the contents to go straight to your chosen section or navigate by using the 'Next'

and 'Back' buttons to the right. Clicking on 'Home' will bring you back to this page.

As part of our policy for continued product development we reserve the right to amend specifications at any time without prior notice.

Home

Back

1. Copyright and Trademarks

The information contained within this manual must not be

reproduced in whole or part without the manufacturer’s prior

written approval.

The manufacturer reserves the right to make changes to

specifications and other information contained in this document

without prior notice.

Pulsair Desktop™ is a registered Trademark of

Keeler Limited 2007.

Published in the UK 2009.

Description of the product

The Pulsair Desktop Tonometer is indicated for measuring

intraocular pressure without contacting the eye to aid in the

screening and diagnosis of glaucoma.

It is an “air puff” Tonometer designed to accurately measure Intra

Ocular Pressure (IOP) without making contact with the surface of

the eye.

Air impulse tonometry is a variant of the general applanation

tonometry in which a portion of the cornea is flexed by

mechanical stimuli in which the force/pressure required to

produce the flexing effect is related to the intraocular pressure.

The air puff technique requires directing a calibrated quantized

packet of air towards the central portion of the cornea, and the

detection of the pre-defined deformation of the cornea through

optical means and reflections from the corneal surface.

Please read and follow these instructions carefully.

Home

Back

2. Introduction

Thank you for purchasing the Keeler Pulsair Desktop.

The product has been designed and manufactured to

ensure that you will enjoy many years of

trouble free and safe use.

Please follow the User Instructions to

ensure optimum performance.

Home

Back

3. Symbols

Read user instructions for Warnings, Cautions and

additional information

The CE mark on this product indicates it has been

tested to and conforms with the provisions noted

within the 93/42/EEC Medical Device Directive

Double insulated

Type BF protections against shock

Consult instructions for use

Manufacturers name and address

Keep dry

USB transfer port

0088

Power input port

On/Off

Colour adjustment

Brightness adjustment

Contrast adjustment

Fragile

This way up

Material suitable for recycling

Home

Back

4. Safety

4.1 Device Classification

CE Regulation 93/42 EEC: Class 2a

FDA: Class II

4.2 Warnings and cautions

Warning

• Do not use if the product is visibly damaged and periodically

inspect for signs of damage.

• Do not use in the presence of flammable gases.

• This product should not be immersed in fluids.

• Do not fit mains power adapter into a damaged mains

outlet socket.

• Route power cords safely to eliminate risk of tripping or

damage to user.

• This equipment should only be used by trained personnel.

USA Federal law restricts this device to sale by or order of a

physician.

• Only use approved Keeler power supply EP29-32777 or

instrument may malfunction.

Caution

• The product has been designed to function safely when at an

ambient temperature between +10ºC and +35ºC.

• Keep out of the reach of children.

• To prevent condensation from forming, allow instrument to

come to room temperature before use.

• Accuracy of IOP measurements is known to be affected by

variations and changes in corneal rigidity due to differences in

corneal thickness, intrinsic structural factors or corneal

refractive surgery. It is recommended that these factors are

considered during IOP measurement.

• Keeler recommends the use of disposable hygienic chinrest

tissues on the chin rest before the patients place their chin

on it.

• This product should be used in a room with subdued lighting

• Before using the Pulsair Desktop, press the 'Clear/Demo'

button for 1 second to dispel any minute particles of dust or

moisture which may have settled whilst the instrument was

not in use.

Home

Back

5. Cleaning instructions

Only manual non-immersion cleaning as described should

be used for this instrument. Do not autoclave or immerse in

cleaning fluids. Always disconnect power supply from source

before cleaning.

Wipe the external surface with a clean absorbent, non-

shedding cloth dampened with a water / detergent solution

(2% detergent by volume) or water / isopropyl alcohol

solution (70% IPA by volume). Avoid optical surfaces.

b Ensure that excess solution does not enter the instrument.

Use caution to ensure cloth is not saturated with solution.

c Surfaces must be carefully hand-dried using a clean non-

shedding cloth.

d Safely dispose of used cleaning materials.

Home

Back

6. Power supply assembly

Set Plug

Replace the blanking plate with the appropriate mains plug

adapter if required, or use IEC 60320 TYPE 7 connector

(not supplied).

IEC 60320 TYPE 7 connector

Home

Back

7. Mounting

Your Pulsair Desktop is designed to be used on a sturdy flat

surface, for example a medical instrument table or a purpose

designed refraction system table top.

Choose carefully the intended location for your Pulsair Desktop

with particular consideration to health and safety aspects, for

example the routing of the power lead, and it’s position in

regard to the user and the patient.

Your Pulsair Desktop has four anti slip rubber feet, ensure these

are located well within the edge of your intended flat surface to

ensure there is no possibility of the Pulsair becoming dislodged

and causing injury to a user or patient.

Your Pulsair Desktop has an adjustable chinrest, however we

recommend that to ensure maximum patient comfort you use it

on a height adjustable table that allows wheelchair access for any

wheelchair bound patients.

Home

Back

Anti slip rubber feet

Home

Back

8. Tonometry, pressure variations in the human eye

The Keeler Pulsair Desktop measures intra-ocular pressure by

automatically releasing a gentle puff of air onto the cornea.

This is known as an event.

A single reading can sometimes be misleading as the IOP will

vary as a result of pulse, respiratory and diurnal fluctuations. In

addition blinking, squeezing, fluid intake, physical activity, body

position and even the direction of gaze can influence IOP.

Up to 4 readings may be required in order to reduce the impact

of these variants to a constant IOP.

Pulsair Desktop software will recognise the readings and give

a sound notification when two consecutive readings are +/-

1mmHg of each other indicating that further measurements may

not be required.

Home

Back

1. Travelling lock

The Pulsair Desktop is fitted with a travelling lock to protect

the moving parts from damage when in transit or when the

device may be subject to sudden movement or shock.

To release the travelling lock rotate it counter clockwise until the

joystick assembly is free to move.

To lock the moving section in place, align the moving upper

section with the base unit and carefully screw the travelling lock

clockwise until it is firmly located.

Note – do not over tighten the travelling lock.

2. Chinrest and chinrest height adjuster

Rotate the chinrest adjuster to increase or decrease the

height of the chinrest until the patients outer canthus is in line

with the indicator line on the chinrest vertical bar.

3. On/Off push button

On pressing the On/Off button, the instrument

will be switched on and ready for use. The

display will progress quickly through the

following stages during system initialisation.

9. Names of controls and components

R : R E A DY

L:READ Y

When the system is ready to use, the display will read L: Ready or

R: Ready depending on whether the tonometer is in position

to test the left eye or the right eye.

R indicates it is in the right eye position – the display could also read

4. Start/Stop button

Pressing this button while the Pulsair Desktop

is running will stop the pump and put the

system into standby mode, the display will

show Standby. The Start/Stop button will reset the memory buffer,

clearing all readings stored. Pressing this button while the unit is

on standby, the Pulsair Desktop will start with the pump running

and the system is initialised ready for use. The instrument will go

through all the displays as per section 3.

5. Motion sensitive wakeup mechanism

The Pulsair Desktop is equipped with a motion sensor. Upon

moving the platform from left to right or vice versa, the motion

sensitive switch is activated to start the pump and the rest of the

system from Standby mode so that it is ready for measurement

use. The instrument will go through all the displays as per

section 3. After two minutes of inactivity the system

automatically switches off to save energy.

6. Clear/Demo button

Pressing the Clear/Demo button

momentarily clears all records of

previous readings and the instrument is

set to its default setting. If this button is pressed and held

for more than a second, the instrument initialises and puffs

a demo puff in order to demonstrate to the patient the

softness of the air puff.

CLEARING

DEM O PUFF

STARTI N G

KEELER PU LSAIR

O K

Home

Back

Home

Back

9. Names of controls and components

7. Print/Menu button

Pressing the Print/Menu button

momentarily will print the results on the

integrated printer and send the data to

the USB data port. If this button is pressed

and held for more than a second, a user

selectable menu option is entered.

8. Easy Pulse Button

Pressing and holding this button for over

a second activates the ‘Easy Pulse’ mode.

This enables the instrument to fire

in the event of difficulties in firing, for example, with a

damaged or scarred cornea. This action is accompanied by

sound and an additional momentary indication on the display.

On pressing any other button or changing the eye, the

instrument resets to normal mode.

9. USB transfer port

This is used for transferring

IOP data to an external device

such as a personal computer

and for use by a qualified

technician when

calibrating the Pulsair

Desktop or performing

a software revision.

10. Power input connection/

disconnection

To connect, insert the low voltage power lead into the

power input socket. To disconnect, remove the low voltage

power lead from the power input socket.

11. Joystick

The rotating joystick controls the elevation of the

measurement head and back front movements of the moving

upper section of the Pulsair Desktop.

N O D ATA

PRINTING

E A SY PUL SE

Home

Back

12. Printer cover

Access to the printer paper is via this cover, use your finger in

the lip on the top of the cover and gently pull towards you to

open the printer cover.

13. Alignment screen

The alignment screen allows the user to visualise the

patient’s eyes in order to correctly align the instrument

with the centre of the cornea prior to measurement.

Alignment is performed using the moving part of the

Pulsair Desktop and the joystick for final alignment.

The Pulsair Desktop will fire automatically when correctly

positioned and aligned. See section 10 for detailed instructions

on the alignment process.

14. Alignment screen adjustment

control wheels

Refer to Section 3 for information

on the function of these three

control wheels.

9. Names of controls and components

Home

Back

15. Measurement display screen

Measurement display screen – This screen will display the Eye

measured, the average reading and individual readings

from either the left (L) and right (R) eyes. Left and right

detection is automatic.

After the first reading is taken the display shows the

measured IOP. After each of the consecutive readings are

taken the display shows the individual reading and the

average of up to the last four 4 readings per eye.

In addition to IOP readings, the Pulsair Desktop also displays a

number of messages on the character display when a

measurement is not detected for a number of reasons. In

such cases, the display may read as follows:

a) < 5: This is shown when the reading is lower than 5mmHg, in which case no valid reading is displayed. (Signified by long sound)

b) >25: This is shown when applanation is detected with soft-puff and the reading is greater than 25mmHg, in this case the instrument displays >25 and switched to hard puff. The instrument shall stay in hard puff until two consecutive readings are less than 20mmHg.

c) >50: This is shown when the reading is greater than 50mmHg, in which case no valid reading is displayed. (Signified by long sound)

Note: The displayed dummy average is rounded to the nearest whole number or displayed to one decimal place depending on the user setting accessed via the menu.

The displayed running average is based on the actual readings

which are taken to one decimal place. For example, readings of

15.4, 16.3, 14.2 and 16.9 are averaged by adding them together

which equals 62.8 and dividing by the number of readings taken, 4.

This gives a final figure of 15.7, or 16 depending on user settings.

Please note independent readings are displayed as whole numbers.

When all the required readings have been taken the figure

displayed is the IOP that is recorded for the patient. When two

consecutive readings are within 1mmHg

an audible sound will be heard indicating

that sufficient readings may

have been taken.

9. Names of controls and components

R : 1 6 : 16 16 16 1 6

Home

Back

10. Measurement procedures

Home

10.1 Preparing the device

1. Plug in the power supply cord to the instrument. The power socket is

located on the right hand side of the instrument.

2. Turn the instrument on using the on/off push switch located on the

front of the instrument. To initialise the instrument ready for use.

3. Remove the protective dust cap from the puff tube.

4. Unscrew the transit lock if secured.

5. Using the joystick bring the moving part of the Pulsair Desktop back

towards you and across to the left (to measure the right eye first).

6. Before using the Pulsair Desktop, press the 'Clear/Demo' button for

1 second to dispel any minute particles of dust or moisture which may

have settled whilst the instrument was not in use.

Home

Back

Home

10.2 Preparing the patient

Before using the Pulsair Desktop you should make your patient

feel at ease and ensure they are located in an optimum reading

location, preferably with their head supported. This is because

apprehension and nervousness may adversely affect the readings

obtained. Follow the points outlined below to achieve this:

Ensure that the patient is comfortable and in a relaxed

position.

2. Ask the patient to remove their contact lenses or spectacles if

worn and to blink and breathe normally.

3. In order to reassure the patient, you can demonstrate the

procedure, using the Demo button, on the back of the

patient’s hand prior to taking a reading.

4. Place disposable chinrest tissue on the chin rest.

Ask the patient to place their head on the chinrest.

5. Adjust the chinrest height so that the outer canthus is

aligned with the marker on the chin rest vertical support.

Before taking a reading you should:

1. Ask the patient to blink to ensure a good and reflective tear film.

Ensure the patient and instrument optics are not positioned

under direct lighting (i.e. spot lights or sunlight).

3. Ensure the patient’s eyes are fully opened. This helps to

prevent squeezing, where the patient unconsciously tenses

their eyelids and increases IOP.

4. Throughout the reading process, you should:

Allow the patient to blink at intervals in order to maintain

the corneal tear film.

10. Measurement procedures

Home

Back

10. Measurement procedures

10.3 Taking the reading

1. Holding the joystick, move with the other hand the moving part of

the Pulsair Desktop until the patient’s eye to be measured is visible and

central on the alignment video screen. Height adjustment is obtained by

rotating the joystick. If there is insufficient travel re-check the patients

head height in the chinrest and try again using the joystick

2. Carefully move the tonometer towards the patient until the external eye

image becomes the cross hairs alignment target

3. Using the joystick, focus the cross hair alignment target until the correct

focused position triggers the tonometer to fire automatically.

4. Remain in the firing position until the Pulsair stops reading, after four

readings per eye are taken. The Pulsair Desktop will indicate with a short

beep when sufficient readings may have been taken i.e. when two

successive readings are within +/- 1mmHg of each other.

5. If a reading is recorded as a non event or bad event, a bad event long tone

will be heard.

6. The first reading will be the measured value; successive readings will display

the running average IOP. Outlying or spurious readings will automatically be

excluded from the calculation.

Home

Back

11. Display examples

STARTI N G ....... .

R U N SELF TEST?

SELFTEST RU N N I N G

R : 1 6 : 16 16 16 1 6

STARTI N G

KEELER PU LSAIR

O K

The unit will display ‘STANDBY’ when the power is on.

The unit will display ‘STARTING’ while the system initialises.

Individual readings, along with the running average (on the left

hand side of the display) of measurements taken so far will be

displayed. The decimal point in the running average is selectable

by the user. i.e. ’16.5’: if the xx.x setting is selected in the SET

IOP Format or 16 is displayed if xx is selected through the menu

system (refer to section 14). Outlying or spurious readings will

automatically be excluded from the calculation.

When a pressure (IOP) of less than 5mmHg is detected, the unit

will display ‘<5 READ AGAIN’.

When a pressure (IOP) of greater than 25mmHg is detected, the

unit will display >25. When a pressure (IOP) of greater than

50mmHg is detected, the unit will display >50. In each case, the

puff intensity will automatically be increased from the soft puff

to the normal puff level for subsequent measurements. In these

cases the user does not need to reset the instrument.

A self test program can be run for diagnostic purpose by

selecting the Menu Option. The display will show run self test.

By pressing the Clear/Demo button self test is entered and the

display will show self test running, and this will run for 45

seconds. At the end of the test the resulting data is

sent to the printer and the display

is cleared.

Home

Back

12. Printing

The results can be printed by pressing the print button at any

time. Printing the results does not clear the print memory buffer.

USB data out

Pressing the print button sends a flat file to

the usb port in the following format:

[R] : xx, xx, xx, xx, [xx.x]

[L] : xx, xx, xx, xx, [xx.x]

This data may be able to be imported

into other applications, for details of

how to perform this please consult your

third party program support team.

PRINT BUTTON

Home

Back

13. Replacing the printer paper

1. Access to the printer paper is via the printer cover, use your

finger in the lip on the top of the cover and gently pull

towards you to open the printer cover.

Remove the empty paper roll.

2. Place the new roll of paper into the paper holder, making sure

the free end is loose at the top of the roll, otherwise it won’t

print.

3. Feed the free end of paper through the gap in the cover.

4. Close the cover.

Home

Back

14. User menu options

1. With the unit switched on, press and hold the ‘print/menu’ button

for > 3 second to enter the user menu.

2. The display will show the first Menu Option (Buzzer Control) and

the current selection (ie. [BUZZER ON] or [BUZZER OFF])

3. Pressing the ‘clear/demo’ button for < 1 second, cycles through the

user Change Options (shown in table.)

4. Pressing the ‘print/menu’ button for < 1 second moves you forward

to the next Menu Option (shown in table), in this case the Desktop

Level.

5. Use the ‘clear/demo’ button to make your preferred selection.

6. Continue to repeat steps 4 and 5 until ‘OK’ is displayed. Your Pulsair

Desktop is now ready to use with your preferred settings.

Menu option Display Change options

Buzzer Control BUZZER ON ON/OFF

IOP Format DISPLAY XX XX / XX.X

Display Screen CONTRAST 0 0 - 20

Full Self Test

RUN SELF TEST? RUNNING SELF TEST

Home

Back

15. Calibration, maintenance and inspection

Clean the puff tube lens on a weekly basis:

1. Moisten a cotton bud with Isopropyl Alcohol.

2. Move the tip of the bud around the lens in a circular motion.

3. After one circle the bud should be discarded to avoid

smearing on the lens.

4. Look at the puff tube lens from the patient’s side, if traces of

tear film can still be seen, repeat above steps until clear.

Note: Care should be taken not to damage the Puff Tube

assembly during cleaning.

Caution

Never use a dry cotton bud or tissue to clean the puff tube lens.

Never use a silicone impregnated cloth or tissue to clean the

puff tube lens.

External cleaning

Keep the unit free of dust.

Keep the chinrest and forehead rest clean.

Regular inspection

Inspect your power supply unit and cable for damage regularly.

Before inspecting, disconnect the power supply from the Pulsair

Desktop and the mains.

If the outer insulation of the cable appears to be damaged

discontinue use immediately. Contact your

local dealer for a replacement.

Home

Back

15. Calibration, maintenance and inspection

General

Keep the instrument free from dust.

If the unit is to remain unused for any length of time, press the

On/Off push button switch to Off and remove the power supply.

Use the dust cover to protect the unit.

Servicing and calibration

Keeler recommends an annual calibration for the Tonometer.

Do not modify this equipment without authorisation of the

manufacturer.

This must be performed by an authorised Pulsair service centre

or distributor. The unit performs a self function check when

switched on and will indicate if a fault is found.

There are no user serviceable parts in this instrument. Service

manuals will be available to authorised Keeler service centres

and Keeler trained service personnel.

Home

Back

16. Specifications and electrical ratings

Dimensions 450 x 435 x 245mm (H x D x W)

Weight 16kg

Calibrated range 5mmHg to 50mmHg

Repeatability (Average <5% coefficient of variation)

Accuracy +/-5mmHg (95% confidence level)*

Working distance 20mm from surface of patient’s cornea to front surface of first lens. This equates to a nominal distance of

15mm from the front of the puff tube shroud to the front surface of the patient’s cornea

Displayed scale Single line 16 character alphanumeric display

Illumination system LED infra red

Complies with Electrical Safety (Medical) BS EN 60601-1:2006. Electromagnetic compatibility EN 60601-1-2:2007

Ophthalmic instruments - fundamental requirements and test methods ISO 15004-1:2006 Optical radiation hazard ISO 15004-2:2007

Power Supply Unit Switch mode, (110 – 240V)+/- 10% multi plug type compliant to EN 60601-1, EN 61000-6-2, EN 61000-6-3

Power supply output 30 VA (12V DC 2.5A)

Frequency 50/60 Hz

Environment Use: +10°C to +35°C, 0% to 75% relative humidity, 700hPa to 1060hPa atmospheric pressure

Storage: -10°C to +55°C, 10% to 95% relative humidity, 700hPa to 1060hPa atmospheric pressure Transport: -10°C to +60°C, 10% to 95% relative humidity, 500hPa to 1060hPa atmospheric pressure

*In house trial carried out on 20 participants

Home

Back

It is well established that exposure of the eye to intense light

sources for extended periods of time poses a risk of retinal photic

injury. Many ophthalmic instruments illuminate the eye with

intense light. The light levels on the Pulsair have been set at the

lowest level possible.

No visible retinal lesions have been identified as a result of using

Pulsair tonometers, however, young children and persons with

diseased eyes may be at a higher risk. The risk may also be slightly

increased if the person being examined has had any exposure with the

same instrument or an other ophthalmic instrument using an intense

visible light source during the previous 24 hours. This will apply

particularly if the eye has been subjected to retinal photography.

16. Specifications and electrical ratings

Parameter Wavelength (nm) Value Measured Limit Units

S-CL

250-400 8.98E-4 0.4 µW cm

-2

UV-CL

360-400 8.11E-7 1 mW cm

-2

A-R

305-700 3.52E-2 220 µW cm

-2

IR-CL

770-2500 8.42E-3

mW cm

-2

VIR-R

380-1400 1.23E-1

0.7

W cm

-2

Red LED

Parameter Wavelength (nm) Value Measured Limit Units

S-CL

250-400 4.53E-5 0.4 µW cm

-2

UV-CL

360-400 4.85E-8 1 mW cm

-2

A-R

305-700 0.24 220 µW cm

-2

IR-CL

770-2500 1.78E-4

mW cm

-2

VIR-R

380-1400 2.69E-5

0.7

W cm

-2

White LEDs

Home

Back

The Keeler Desktop tonometer is a medical electrical instrument. The instrument requires special care concerning

electromagnetic compatibility (EMC).This Section describes its suitability in terms of electromagnetic compatibility of

this instrument. When installing or using this instrument, please read carefully and observe what is described here.

1. Portable or mobile-type radio frequency communication units may have an adverse effect on this

instrument, resulting in malfunctioning.

16. Specifications and electrical ratings

Guidance and manufacturer’s declaration – electromagnetic emissions

The Keeler Desktop is intended for use in the electromagnetic environment specified below. The customer or user should assure that it is used in such an environment.

Emissions test Compliance Electromagnetic environment - guidance

RF emissions CISPR 11

Group 1 The Keeler Desktop uses RF energy only for its internal

function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF emissions CISPR 11

Class A The Keeler Desktop is suitable for use in all establishments

other than domestic and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

Harmonic emissions IEC 61000-3-2

Class A

Voltage fluctuations / flicker emissions IEC 61000-3-3

Complies

Home

Back

16. Specifications and electrical ratings

Guidance and manufacturer’s declaration – electromagnetic immunity

The Keeler Desktop is intended for use in the electromagnetic environment specified below. The customer or user should assure that it is used in such an environment.

Immunity test IEC 60601 Test level Compliance level Electromagnetic environment - guidance

Electrostatic discharge (ESD). IEC 6100-4-2

± 6 kV contact

± 8 kV air

± 6 kV contact

± 8 kV air

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

Electrical fast transient/burst. IEC 61000-4-4

± 2 kV for power supply lines ± 1 kV for input/output lines

Mains power quality should be that of a typical commercial or hospital environment.

Surge. IEC 61000-4-5

± 1 kV line(s) to line(s) ± 1 kV line(s) for line to earth

Mains power quality should be that of a typical commercial or hospital environment.

Voltage dips, short interruptions and voltage variations on power supply input lines. IEC 61000-4-11

<5% U

(> 95% dip in UT)

40% U

(60% dip in UT ) for 5 cycles

70% U

(30% dip in U

) for 25 cycles

<5% U

(>95% dip in UT) for 5 s

<5% U

(> 95% dip in UT)

40% U

(60% dip in UT) for 5 cycles

70% U

(30% dip in UT ) for 25 cycles

<5% U

(>95% dip in UT ) for 5 s

Mains power quality should be that of a typical commercial or hospital environment. If the user of the Keeler Desktop requires continued operation during power mains interruptions, it is recommended that the instrument be powered from an uninterruptible power supply.

Power frequency (50/60 Hz) magnetic field. IEC 61000-4-8

3 A/m 3A/m Power frequency magnetic fields should be at

a level characteristic of a typical location in a typical commercial or hospital environment.

Note UT is the a. c. mains voltage prior to application of the test level.

Home

Back

16. Specifications and electrical ratings

Guidance and manufacturer’s declaration – electromagnetic immunity

The Keeler Desktop is intended for use in the electromagnetic environment specified below. The customer or user should assure that it is used in such an environment.

Immunity test IEC 60601 Test level Compliance level Electromagnetic environment - guidance

Conducted RF IEC 61000-4-6

Radiated RF IEC 61000-4-3

3 Vrms

3 V/m

80MHz to 2.5GHz

3 V

3 V/m

Portable and mobile RF communications equipment should be used no closer to any part of the Keeler Desktop, including cables, than the recommended separation distances calculated from the equation applicable to the frequency of the transmitter.

Recommended separation distance

d = 1.2 √ p

d = 1.2 √ p 80MHz to 800 MHz

d = 2.3 √ p 800MHz to 2.5GHz

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 survey¹, should be less than the compliance level in each frequency range.²

Interference may occur in the vicinity of equipment marked with the following symbol:

Note 1 At 80MHz and 800MHz, the higher frequency range applies. Note 2 These guide lines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures,

objects and people. ¹ Field strengths from fixed transmitters, such as base stations ( 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 Keeler Desktop is used exceeds the applicable RF compliance level above, the Keeler Desktop should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orientating or relocating the Keeler Desktop. ² Over the frequency range 150kHz to 80 MHz, field strengths should be less than 3 V/m.

Home

Back

16. Specifications and electrical ratings

Recommended separation distances between portable and mobile RF communications equipment and the Keeler Desktop

The Keeler Desktop is intended for the use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Keeler Desktop can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Keeler Desktop as recommended below, according to the maximum output power of the communications equipment.

Rated maximum

output power of

transmitter

Separation distance according to frequency of transmitter

50 kHz to 80MHz

d = 1.2√ p

80MHz to 800MHz

d = 1.2√ p

800MHz to 2.5GHz

d = 2.3√ p

0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.74

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 determined 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 80MHz and 800MHz, the separation distance for the higher frequency applies. Note 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects

and people.

Home

Back

17. Accessories and warranty

Accessories supplied

Dust cover Part Number EP39-70435

Chinrest paper pins (2) Part Number 2417-P-7006

Puff tube dust cap Part Number EP39-70433

Consumables

Chinrest papers Part Number 3104-L-8201

Printer Paper Part Number 2208-L-7008

Pulsair Warranty

The Pulsair Desktop and its components are covered by warranty

that they meet their performance standards and are free from

any defects in materials or workmanship. Within 2 years from

delivery by Keeler, the manufacturer shall at no charge to the

customer, upon written notice from the customer, repair or

replace any components which are defective in material or

workmanship.

The customer agrees that it shall have no remedy in the event

of any breach of the foregoing warranty other than as provided

above. This warranty is exclusive and in lieu of all other

warranties, expressed or implied, and all implied warranties of

merchantability or fitness for a particular purpose are expressly

disclaimed.

The obligations of the manufacturer as set forth in this warranty

are expressly conditioned on the following:-

(i) No alterations or repairs of any malfunction of the system

shall be made to the system except by the manufacturer or his

authorized representative, without the prior written approval

of the manufacturer or his authorized representative (and in no

case will the manufacturer assume responsibility for repairs or

alterations made by those other than the manufacturer or his

authorized representative).

And (ii) The customer shall give notice to the manufacturer

or their authorized representative of any malfunction of the

system and shall not use the system for any diagnostic purpose

thereafter.

Home

Back

18. Contact, packaging and disposal information

EP59-70019 Issue D

Disposal of old Electrical and Electronic Equipment

(Applicable in the European Union and other European Countries with

separate Collection Systems).

This Symbol on the Product or on its Packaging and instructions

indicates that it was put on the market place after August 2005 and

that this product shall not be treated as Household Waste.

To Reduce the Environmental impact of WEEE (Waste Electrical Electronic

Equipment) and minimise the volume of WEEE entering landfills we

encourage at Product end of life that this Equipment is recycled and reused.

If you need more information on the collection reuse and recycling then

please contact B2B Compliance on 01691 676124 (+44 1691 676124).

0088

Manufacturer

Keeler Limited Clewer Hill Road Windsor Berkshire SL4 4AA

Freephone: 0800 521251 Tel: +44 (0) 1753 857177 Fax: +44 (0) 1753 827145

USA Sales Office

Keeler Instruments Inc 3222 Phoenixville Pike Building #50 Malvern, PA 19355 USA

Toll Free: 1 800 523 5620 Tel: 1 610 353 4350 Fax: 1 610 353 7814

Keeler Pulsair Desktop Instructions For Use Manual

Specifications and Main Features

Frequently Asked Questions

User Manual