Neopuff Technical Manual Rev M 2011

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Infant Resuscitation | Technical Manual

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1. Specifications

1.1 Warnings

Input gas flow rate 5 to 15 L/min. Recommended operating gas

flow rate 8 L/min. Input flow ranges are circuit specific, refer to

circuit User Instructions.

Do not use oil, grease or other substances that are incompatible

with oxygen on any part of the F&P Neopuff / Perivent

T-Piece Circuit.

Do not attempt to use a higher gas flow rate than 15 L/min.

Incorrect use can be hazardous.

Factory setting of pressure limit valve is at 40 cmH2O. This setting

is user adjustable up to 80 cmH2O. Do not attempt to set the

pressure relief valve above 80 cmH2O. Reset pressure relief valve

to 40 cmH2O after use (refer section 3.3.3 of this manual).

The device must not be used on unattended patients.

Use only recommended F&P Neopuff™ / Perivent™ Infant

Resuscitator accessories.

To be used for resuscitation only.

The operation of the F&P Neopuff / Perivent must be checked prior

to first use.

Refer to section 3.3 “Testing of the F&P Neopuff / Perivent

Performance”.

Use only a F&P gas supply line or approved equivalent.

1.2 Performance Specifications

Peak Inspiratory Pressure (PIP) Range

1.3 Technical Specifications

Height

250 mm (9.8”)

@ 5 L/min

approx. 2 to 70 cmH2O [mbar]

Width

200 mm (7.9”)

@ 8 L/min

approx. 3 to 72 cmH2O [mbar]

Depth

104 mm (4.1”)

@ 10 L/min

approx. 4 to 73 cmH2O [mbar]

Weight

1.9 kg (4.2 lb)

@ 15 L/min

approx. 8 to 75 cmH2O [mbar]

Manometer Range

-10 to 80 cmH2O [mbar]

Manometer Accuracy

+/-2.0% of Full Scale Deflection

Maximum Pressure Setting

65 to 80 cmH2O [mbar]

(dependent on flow rate)

Positive End Expiratory Pressure (PEEP) Range

@ 5 L/min

approx. 1 to 6 cmH2O [mbar]

@ 8 L/min

approx. 1 to 10 cmH2O [mbar]

900RD010 / 900RD110 Dead Space

6 ml

@ 10 L/min

approx. 2 to 15 cmH2O [mbar]

RD1300-10 Dead Space

3.3 ml

@ 15 L/min

approx. 4 to 17 cmH2O [mbar]

Storage Temperature Range

-10 to 50 °C (+14 to +122 °F),

up to 95% humidity

Input Gas Flow Range

Minimum

5 L/min

Maximum

15 L/min

Operating Time (400 L Cylinder)

5 L/min

80 minutes

10 L/min

40 minutes

15 L/min

26 minutes

Operating Temperature Ranges

Humidified Circuit

+18 to 26 °C (+64 to +78 °F),

30 - 75% humidity

Non-Humidified Circuit

-18 to 50 °C (-0.4 to +122 °F),

up to 95% humidity

Recommended Patient

Body Weight

Delivered Oxygen Concentration

0 to 10 kg (22 lb)

Up to 100% depending on gas

supply

NOTE: All performance figures listed above are representative only.

PEEP values stated are based on typical clinical PIP settings.

Higher PEEP values can be achieved if higher PIP values are set.

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1. Specifications continued

1.4 Symbol Definitions

SYMBOL

DEFINITION

1.5 Label Identification

The label pictured is typical of the information contained on a

F&P Neopuff™ / Perivent™ Infant Resuscitator.

Attention: Consult the Operating

Instructions

MAX-P

PiP

Sets the Max Pressure Relief that may

be delivered to the patient

(factory set at 40 cmH2O)

Controls the Peak Inspiratory Pressure

delivered to the patient

5-15 L/min

Gas inlet connection from gas supply

(5 to 15 litres per minute)

REF Gas outlet connection to patient

LOT SN -

This details the product code which identifies the operating

instruction language and fascia type

The production date: (10) = 2010, (06) = June,

(15) = fifteenth day

The serial number is specific to a particular F&P Neopuff /

Perivent Infant Resuscitator. The first six digits match the LOT

number and last six digits identify the specific product serial

number.

The bar code consists of the following predefined application identifiers:

01

- Not used

0 - Sequence start

94 - Country of manufacture - New Zealand

200124 - Company Identifier - Fisher & Paykel Healthcare Ltd

1093 - Product Code

1 - Check Sum

REF - RD900XXX

RD900

XXX

Operating Instruction Language

Fascia Type

900 Series

AEU

English

English Text

ADU

Danish

AFU

French

Symbols

Only

ALU

Italian

AMU

Finnish

ANU

Dutch

ASU

Spanish

ATU

Portuguese

AVU

Norwegian

AWU

Swedish

AZU

Chinese

AGU

German (Perivent)

T-Piece

Resuscitator

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2. Cleaning

• Comply with hospital, local and national guidelines for product

cleaning frequencies.

• Ensure all oxygen and air supplies are turned off and disconnected

from the F&P Neopuff™ / Perivent™ Infant Resuscitator before

performing cleaning procedures. Explosion and fire hazards can

exist when performing cleaning procedures in an oxygen-enriched

environment.

• Cleaning shall be performed at ambient conditions.

• Before cleaning, remove and discard all used disposable products

using the recommended method of disposal.

• Dust all surfaces with a clean damp soft cloth.

• Clean all plastic surfaces with detergent-based solution (maximum

2% in water) ensuring the manufacturer’s directions for use of the

cleaning agent are followed.

• The following proprietary chemical cleaning wipes are

recommended if the F&P Neopuff / Perivent fascia requires cleaning

for infection control purposes.

Caviwipes (Metrex Research Corporation)

Sani-cloth HB (Professional Disposables, Inc.)

Asepti-Wipes II (Ecolab, Inc.)

Spartan’s TB-Cide Quat Wipes

Vernacare Tuffie Wipes Alcohol Free

• Dry all surfaces after cleaning with a clean soft cloth or

paper towel.

CAUTION: Ensure no part of the F&P Neopuff / Perivent Infant

Resuscitator or related accessories is immersed in any cleaning liquid

or cleaning solution. For Test Lung cleaning instructions, see section

2.2.2.

CAUTION: Do not clean the F&P Neopuff / Perivent Infant Resuscitator

fascia with proprietary cleaning products containing either

hydroxides, hypochlorites, peroxides, gluteraldehyde or cleaning

products with a greater than 30% alcohol base.

NOTE: The recommended chemical cleaning wipes listed above have

been checked for long-term compatibility with the IW900 Series Infant

Warmers and the F&P Neopuff / Perivent Infant Resuscitator.

2.1 Cleaning Products to Avoid

CAUTION: The chemicals used in these proprietary cleaning products

may lead to discoloration, crazing and eventual cracking of the fascia.

Examples of proprietary cleaning products which contain such

cleaning chemicals include but are not limited to:

Asepti-Wipes (Ecolab, Inc)

Clorox (The Clorox Company)

Endbac 256 (Johnson Wax Professional)

Quat (3M)

Sporiciden (Liberty Industries, Inc)

Sporox II (Sultan Healthcare)

Steris (Steris Corporation)

Terralin (Schülke & Mayr)

Virtek (A Virtek Company)

Virox (Virox Technologies)

CAUTION: Do not use abrasive cleaning solutions.

CAUTION: Ensure F&P Neopuff/ Perivent Infant Resuscitator and

accessories are checked before returning the Infant Resuscitator to

service.

2.2 Cleaning of the Test Lung

If required, the Test Lung can be disinfected. There are two different

models of Test Lung and each has specific cleaning methods.

• T he Test Lung is a consumable item. Irrespective of model, the

Test Lung should regularly be inspected for signs of damage such

as discoloration, perishing or cracking. Replace the Test Lung if

damage is observed.

2.2.1 Latex (black) Test Lung (discontinued May 2007)

WARNING The Test Lung contains natural rubber latex that may

cause allergic reactions.

CAUTION: Latex is susceptible to attack by solvents. Ensure no solvents

are used to clean the Test Lung.

This Test Lung consists of two parts, the flexible latex test lung and

a rigid black plastic connector. The Test Lung can be disassembled

for disinfection. It can be disinfected using ethylene oxide gas only.

Some carrier gases can cause stress cracking and are not suitable. If

in doubt, check with the chemical supplier.

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2. Cleaning continued

2.2.2 Silicone (blue) Test Lung RD020-01

The Test Lung must be cleaned before every use or in

accordance with hospital cleaning protocols. This test lung consists of

two parts, the flexible silicone test lung and a rigid plastic connector.

The two parts of the Test Lung may be disassembled

for disinfection. It can be cleaned using disinfectants containing

either peracetic acid (e.g. Perasafe®) or orthopthaldehyde

(e.g. Cidex® OPA). Other disinfection methods can cause damage

to the Test Lung and are not recommended.

Please follow the manufacturer’s instructions for storage, handling

and usage of these chemicals.

2.4 Sterilization

CAUTION:

• Do not autoclave or gas-sterilize any part of the

F&P Neopuff™ / Perivent™ Infant Resuscitator.

• Do not autoclave any of the Neopuff / Perivent accessories,

e.g. Test Lung and Gas Supply Line.

• For cold sterilization: Ensure the cold sterilization agents are safe

for use with the relevant surfaces.

2.5 After Cleaning

CAUTION:

• Ensure all F&P Neopuff / Perivent Infant Resuscitator parts and

accessories are checked before returning the device to service.

Silicone Test Lung

Plastic Connector

WARNING Ensure the silicone Test Lung and plastic connector are

both removed from the T-Piece before use on a patient.

2.3 Cleaning Reusable T-Piece

(discontinued September 2008)

The reusable T-Piece 500RD104 consists of two parts and can be

disassembled for disinfection (refer diagram). The T-Piece should

be disinfected by autoclaving at up to 136 °C, 220 kPa for 4

minutes. Following reassembly, the T-Piece should be tested prior

to use to ensure that it is functioning correctly. Refer to the F&P

Neopuff™ / Perivent™ Operating Manual (Fisher & Paykel Healthcare

Part No. 185041726) for set-up instructions.

Unscrew PEEP cap for disinfection

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3. Service Information

3.1 Functional Schematic

3.3 Testing of the F&P Neopuff™ /Perivent™

Performance (Manometer and Valve System)

Circuit Pressure Manometer

Gas Inlet Port

Gas Outlet Port

Manometer

Maximum

Pressure

Relief Valve

Peak

Inspiratory

Pressure Valve

3.2 Installation Checks and Preventative

Maintenance

WARNING Dropping the F&P Neopuff™ / Perivent™ Infant

Maximum

Pressure

Relief Cover

Peak

Inspiratory

Pressure

Control

Inlet Port

Outlet Port

Resuscitator or other similar forms of impact may cause damage

resulting in incorrect operation of the unit. If you suspect damage

to have occurred, please perform checks as outlined in section 3.3

before connection to a patient.

3.2.1 Installation Checks

Prior to first use:

– Remove manometer cover

– Complete Performance Testing (section 3.3)

3.2.2 Preventative Maintenance

The integrity of the F&P Neopuff / Perivent manometer and valve

system can be tested using the following guidelines. The inlet port

must be connected to a gas supply capable of generating constant

flow at 5, 10 and 15 L/min, and a certified gauge and bleed valve

should be available to check the manometer accuracy. The

F&P Neopuff / Perivent resuscitation circuit and T-Piece can

be used in place of a bleed valve as shown below.

• The integrity of the system and manometer should be checked prior

to first use, annually and after servicing, using the

“Testing of the F&P Neopuff / Perivent Performance” procedure

(section 3.3).

Use T-Piece with

Test Lung attached

as a bleed valve

• The use of a mounting bracket to help prevent the

F&P Neopuff / Perivent being damaged or dropped is recommended.

Mounting solutions available can be found in section 5 of this

manual.

50

60 70

40

• All maint­enance and service procedures must be performed by

qualified personnel using only Fisher & Paykel Healthcare parts.

• Always ensure gas passages are free from contaminants, especially

hydrocarbons, oils and grease, prior to reassembly.

30

20

10

80

–

cm

H 2O

+

0 -10

Certified Gauge

50

60 70

40

30

• Please contact an authorized Fisher & Paykel Healthcare

representative for further assistance with any servicing or

maintenance requirements.

• The Test Lung is a consumable item; it should be monitored for

signs of wear and material degradation and replaced as required.

20

10

80

–

0 -10

cm

H 2O

+

-20

Connect pressure gauge

between F&P Neopuff / Perivent

outlet and resuscitation circuit

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3. Service Information continued

3.3.1 Testing of the Manometer

1. L ift the cover off the Max Pressure Relief Valve slightly and turn out

of the way.

2. D

 isconnect all devices from the F&P Neopuff™ / Perivent™ outlet

port. Check that the manometer needle is within +/-2 cmH2O of

zero on the manometer gauge. If the manometer does not read

zero, the resetting of the manometer to zero procedure (section

3.3.4) should be followed.

3. C

 onnect the outlet of the F&P Neopuff / Perivent Infant Resuscitator

to a bleed valve and a certified gauge (e.g. Mensor Digital Pressure

Gauge Series 2400). Set the gas supply to 10 L/min. Completely

close the maximum pressure limit valve by turning the left-hand

knob completely clockwise. With the bleed valve closed, adjust

the Peak Inspiratory Pressure knob to set the pressure so that

the certified gauge reads 10, 20 and 40 cmH2O. Check that the

manometer reads within +/-2 cmH2O of these values at each set

point.

4. W

 ith the pressure set to 40 cmH2O, open and close the bleed valve

three times and check the manometer needle rises and falls

smoothly. If the F&P Neopuff / Perivent Infant Resuscitator

fails any of these tests, the manometer should be regarded

as inaccurate and replaced with a new manometer (Part No.

043040841).

Follow the manometer replacement guidelines in section 3.3.5 of

this manual, or contact your Fisher & Paykel Healthcare service

representative for further guidance.

Alternative settings for the Max Pressure Relief should be made in

accordance with hospital protocol.

1. Adjust gas flow to 10 L/min.

2. C

 lose the Peak Inspiratory Pressure valve by turning the knob fully

clockwise.

3. A

 djust the Max Pressure Relief knob clockwise or counterclockwise

until the manometer reads 40 cmH2O.

4. T urn the Peak Inspiratory Pressure knob counterclockwise so the

manometer reads 20 cmH2O and shut off the gas flow.

3.3.4 Resetting the Manometer to Zero

To set the manometer to zero:

1. D

 isconnect the F&P Neopuff™ / Perivent™ Infant Resuscitator from

any other equipment.

2. Remove the opaque plastic plug in the lens of the manometer.

3. U

 sing a suitable slot screwdriver, carefully adjust the screw in

the manometer face clockwise or counterclockwise to reset the

manometer to zero. Care must be taken when doing this, as overrotation of the screw can damage the manometer internals.

4. Replace the plastic plug in the lens of manometer.

5. V

 erify that the manometer needle is now within +/-2.0 cmH2O of

zero. If not, repeat the above procedure.

3.3.5 Manometer Replacement

The manometer is not a serviceable item and must be replaced by

Manometer Kit 043040841.

1. Remove the back cover, fixed by four screws.

3.3.2 Testing of the Valve System

2. Disconnect the tube from the manometer.

1. S

 et the gas supply to 5 L/min. Completely close the Peak

Inspiratory Pressure control and the Max Pressure control by

turning both knobs completely clockwise. Close the bleed valve

and check that the gauge reads at least 60 cmH2O.

3. Remove the manometer by unscrewing the two retaining nuts.

2. S

 et the gas supply to 15 L/min. Close the bleed valve and check

that the gauge reads no higher than 80 cmH2O.

3. S

 et the gas supply to 10 L/min. Close the bleed valve and turn the

Max Pressure Relief valve until the manometer reads 40 cmH2O.

Check that the manometer needle rises and falls smoothly. Gently

rotate the Max Pressure Relief cover over the Max Pressure Relief

knob.

4. R

 eset the peak inspiratory pressure to 20 cmH2O and turn off the

gas flow. Testing is now complete.

If the F&P Neopuff / Perivent Infant Resuscitator fails any of these

tests, the valve assembly should be regarded as faulty and replaced

with a new valve assembly (see the parts list (section 4.1.2) for

part numbers). Follow the valve replacement guidelines in section

3.3.6 of this manual, or call your Fisher & Paykel Healthcare service

representative for further information.

3.3.3 Setting Max Pressure Relief to 40 cmH2O

This is required if the Max Pressure Relief has been changed. The

factory setting for the Max Pressure Relief is 40 cmH2O.

4. F it the new manometer into the front panel, tighten the retaining

nuts and reconnect the manometer tube.

5. Refit the front panel to the back cover with the four screws.

6. C

 arry out the manometer performance test as per section 3.3.1. It

is recommended to record the lot number from the box label of the

replacement manometer on the maintenance checklist.

3.3.6 Valve System Replacement

NOTE: The valves are an integral part of the valve, panel and

manifold assembly and are not able to be serviced. Please specify

the model number from the parts list (section 4.1.2) when ordering a

replacement valve assembly.

1. Remove the back cover, fixed by four screws.

2. Disconnect the tube from manometer.

3. Remove the manometer by unscrewing the two retaining nuts.

4. F it the existing manometer into the new valve assembly panel,

tighten the retaining nuts and reconnect the manometer tube.

5. Refit the front panel to the back cover with the four screws from

step 1.

6. Carry out the valve system performance test as per section 3.2.2.

It is recommended to record the lot number of the new valve

assembly onto the Set-up and Maintenance Checklist.

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3. Service Information continued

3.4 Set-up and Maintenance Checklist

The following table is provided to record the results of the performance tests described in section 3.3. Any components replaced should be

recorded also, as appropriate. The table may be photocopied or otherwise reproduced as required.

Upon receipt of the product and prior to use on a patient, please complete the tests and fill in the table below.

Name:

F&P Neopuff™/Perivent™

Performance Testing Record

Customer Details

Address:

Country:

Phone Number:

Email:

Test Date:

Serial Number:

For 900IW130 only:

Infant Warmer Serial Number:

Tested By:

Next Test Due Date:

Check

Ref

or x

Comments

Manometer Checks:

Replacement Manometer Serial Number:

Accuracy @ 0 cm (+/-2 cmH2O)

3.3.1-2

Accuracy @ 10 cm (+/-2 cmH2O)

3.3.1-3

Accuracy @ 20 cm (+/-2 cmH2O)

3.3.1-3

Accuracy @ 40 cm (+/-2 cmH2O)

3.3.1-3

Needle movement smooth?

3.3.1-4

Valve System Checks:

Pressure greater than 60 cmH2O?

3.3.2-1

Pressure less than 80 cmH2O?

3.3.2-2

Maximum pressure set to 40 cmH2O

3.3.2-3

PIP reset to 20 cmH2O

3.3.2-4

Additional Comments:

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4. Assembly Diagrams

4.1 F&P Neopuff™ / Perivent™ Infant

Resuscitator (Post June 2010)

4.1.2 Parts List

Units manufactured Post June 2010

This F&P Neopuff / Perivent module contains a sealed valve assembly

that can not be serviced in the field. If a faulty valve occurs, the entire

panel and valve assembly must be replaced.

#

Description

Part Number

Reqd

1

Handle Neopuff Spare

043043976

1

4.1.1 Assembly Diagram

2

Plug (set of four)

693040706

2

3

Screw M8x20

614040309

8

4

End cap (upper)

043042565

1

5

End cap (lower)

043042564

1

6

Back cover

641040816

1

Model specific panel and

valve assembly

(see Spares Kit section 4.1.3)

(see table in

section 4.1.3)

1

7

8

Manometer kit

043040841

1

9

Cap Valve Neopuff Spare (Blue)

043043977

1

10

Cover, maximum pressure relief valve

043041057

1

11

Foot

693041436

4

12

Screw #8x1” Csk

616050011

4

13

Screw M4x8 Pan hd

(handle attachment)

614040117

2

NOTE: White valve cap (pre-June 2010) can be ordered using 043042345

(1 / bag).

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4. Assembly Diagrams continued

4.1.3 Spares Kit

NOTE: All RD900 units manufactured from May 1999 can

accommodate the above spares kit.

Model specific panel and valve assembly Blue (kit includes fascia)

043043595

Fascia & Valve Assy Blue English

043043596

Fascia & Valve Assy Blue German

043043597

Fascia & Valve Assy Blue Italian

043043598

Fascia & Valve Assy Blue Spanish

043043599

Fascia & Valve Assy Blue French

043043600

Fascia & Valve Assy Blue Norwegian

043043601

Fascia & Valve Assy Blue Dutch

043043602

Fascia & Valve Assy Blue Swedish

043043603

Fascia & Valve Assy Blue Portuguese

043043604

Fascia & Valve Assy Blue Danish

043043605

Fascia & Valve Assy Blue Finnish

Model specific panel and valve assembly Purple (kit includes fascia)

043042347

Fascia & Valve Assy English

043042348

Fascia & Valve Assy German

043042349

Fascia & Valve Assy Italian

043042350

Fascia & Valve Assy Spanish

043042351

Fascia & Valve Assy French

043042353

Fascia & Valve Assy Dutch

043042354

Fascia & Valve Assy Swedish

043042355

Fascia & Valve Assy Portuguese

043042356

Fascia & Valve Assy Danish

043042357

Fascia & Valve Assy Finnish

043042358

Fascia & Valve Assy Norwegian

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5. Mounting Options

Impact to the F&P Neopuff™ / Perivent™ Infant Resuscitator,

caused by rough handling or the unit being dropped, can damage the

valve system and produce irregular resuscitation pressures.

To help prevent any impact to the device, Fisher & Paykel Healthcare

recommends the use of one of the mounting systems shown below.

5.2 900MR088 Rail Bracket

For mounting the F&P Neopuff / Perivent Infant Resuscitator centrally

on standard rails (2.5 to 5.5 cm x 1 cm / 0.98 to 2.17” x 0.39”).

Also requires RD050-01.

5.1 900RD301 Side-Mounting Block,

900MR170 C-Clamp, 900MR030 Pole Bracket

The 900RD301 Side Mounting Block fits into the dovetail slot on the

side of the Infant Resuscitator. The 900RD301 may then be connected

to a 17 to 40 mm pole using either the 900MR170 C-Clamp or

900MR030 Pole Bracket.

Mounting Option

Parts to order

Quick disconnect (C-Clamp)

900RD301 & 900MR170

Permanent Pole Bracket

900RD301 & 900MR030

5.3 900RD302 Wall Mount Bracket

The 900RD302 Wall Mount Bracket has two tongue fittings that

may be screwed to the back of the F&P Neopuff™ / Perivent™ Infant

Resuscitator by removing the four plastic plugs from the rear panel,

and a T-shaped bracket that should be screwed to the wall.

This allows the infant resuscitator to be quickly and easily removed

from and replaced on the bracket as required.

900RD301

900MR170

C-Clamp

TLET

GAS OU

GAS INL

ET

in

5-15 L/m

900MR030

Pole Bracket

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5. Mounting Options continued

5.4 RD050-01 Pole and Rail Central Mount

For mounting the F&P Neopuff™ / Perivent™ Infant Resuscitator

centrally on a pole or on standard rails (2.5 to 5.5 cm x 1 cm /

0.98 to 2.17” x 0.39”), a central mounting block can be affixed to

the back of the unit by removing the four plastic plugs from the rear

panel. The unit will then fit the F&P bracket and clamps.

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For more information please contact

your local Fisher & Paykel Healthcare representative

Manufacturer

Fisher & Paykel Healthcare Ltd

15 Maurice Paykel Place

East Tamaki, Auckland 2013

PO Box 14 348 Panmure

Auckland 1741

New Zealand

Tel:

Fax:

Email:

Web:

+64 9 574 0100

+64 9 574 0158

info@fphcare.com

www.fphcare.com

Australia

Tel: +61 3 9879 5022

Fax: +61 3 9879 5232

Austria

Tel: 0800 29 31 23

Fax: 0800 29 31 22

Benelux

Tel: +31 40 216 3555

Fax: +31 40 216 3554

China

Tel: +86 20 3205 3486

Fax: +86 20 3205 2132

France

Tel: +33 1 6446 5201

Fax: +33 1 6446 5221

Germany

Tel: +49 7181 98599 0

Fax: +49 7181 98599 66

185041597 RevM EN © 2011 Fisher & Paykel Healthcare Limited

India

Tel: +91 80 4284 4000

Fax: +91 80 4123 6044

Irish Republic

Tel: 1800 409 011

Italy

Tel: +39 06 7839 2939

Fax: +39 06 7814 7709

Japan

Tel: +81 3 3661 7205

Fax: +81 3 3661 7206

www.fphcare.com

Northern Ireland

Tel: 0800 132 189

Spain

Tel: +34 902 013 346

Fax: +34 902 013 379

Sweden

Tel: +46 8 564 76 680

Fax: +46 8 36 63 10

Switzerland

Tel: 0800 83 47 63

Fax: 0800 83 47 54

Taiwan

Tel: +886 2 8751 1739

Fax: +886 2 8751 5625

Turkey

Tel: +90 312 354 34 12

Fax: +90 312 354 31 01

UK

(EU Authorised Representative)

Fisher & Paykel Healthcare Ltd

Unit 16, Cordwallis Park

Clivemont Road, Maidenhead

Berkshire SL6 7BU, UK

Tel: +44 1628 626 136

Fax: +44 1628 626 146

USA/Canada

Tel: +1 800 446 3908

or

+1 949 453 4000

Fax: +1 949 453 4001