Neopuff Technical Manual

Neopuff Technical Manual
  • Neopuff Technical Manual

  • Views 16

  • Downloads 2

  • File size 2MB
  • Author/Uploader: Carlos Cortes

|

Infant Resuscitation | Technical Manual

TABLE OF CONTENTS

1. Specifications………………………………………………………………………………………………………………………………………………….2 1.1 Warnings………………………………………………………………………………………………………………………………………………………2 1.2 Performance Specifications……………………………………………………………………………………………………………………………..2 1.3 Technical Specifications………………………………………………………………………………………………………………………………….2 1.4 Symbol Definitions…………………………………………………………………………………………………………………………………………3 1.5 Label Identification . ………………………………………………………………………………………………………………………………………3 2. Cleaning …………………………………………………………………………………………………………………………………………………………4 2.1 Cleaning Products to Avoid………………………………………………………………………………………………………………………………4 2.2 Cleaning of the Test Lung…………………………………………………………………………………………………………………………………4

2.2.1 Latex (black) Test Lung (discontinued May 2007) ……………………………………………………………………………………..4

2.2.2 Silicone (blue) Test Lung RD020-01…………………………………………………………………………………………………………5

2.3 Cleaning Reusable T-Piece (discontinued September 2008)…………………………………………………………………………………..5 2.4 Sterilization…………………………………………………………………………………………………………………………………………………..5 2.5 After Cleaning………………………………………………………………………………………………………………………………………………..5

3. Service Information…………………………………………………………………………………………………………………………………………..6 3.1 Functional Schematic……………………………………………………………………………………………………………………………………..6 3.2 Installation Checks and Preventative Maintenance………………………………………………………………………………………………6

3.2.1 Installation Checks……………………………………………………………………………………………………………………………….6

3.2.2 Preventative Maintenance………………………………………………………………………………………………………………………6

3.3 Testing of the F&P Neopuff™/ Perivent™ Performance (Manometer and Valve System)………………………………………………6

3.3.1 Testing of the Manometer………………………………………………………………………………………………………………………7

3.3.2 Testing of the Valve System……………………………………………………………………………………………………………………7

3.3.3 Setting Max Pressure Relief to 40 cmH2O………………………………………………………………………………………………….7

3.3.4 Resetting the Manometer to Zero…………………………………………………………………………………………………………….7

3.3.5 Manometer Replacement………………………………………………………………………………………………………………………7

3.3.6 Valve System Replacement…………………………………………………………………………………………………………………….7

3.4 Set-up and Maintenance Checklist ……………………………………………………………………………………………………………………8

4. Assembly Diagrams…………………………………………………………………………………………………………………………………………..9 4.1 F&P Neopuff™/Perivent™ Infant Resuscitator (Post June 2010)……………………………………………………………………………..9

4.1.1 Assembly Diagram……………………………………………………………………………………………………………………………….9

4.1.2 Parts List…………………………………………………………………………………………………………………………………………….9

4.1.3 Spares Kit…………………………………………………………………………………………………………………………………………10

5. Mounting Options…………………………………………………………………………………………………………………………………………..11 5.1 900RD301 Side-Mounting Block……………………………………………………………………………………………………………………..11 5.2 900MR088 Rail Mount Bracket……………………………………………………………………………………………………………………….11 5.3 900RD302 Wall Mount Bracket……………………………………………………………………………………………………………………….11 5.4 RD050-01 Pole and Rail Central Mount…………………………………………………………………………………………………………….12

N E O P U F F ™ t e c h n i c a l m a nu a l

1

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.

N E O P U F F ™ t e c h n i c a l m a nu a l

2

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)

Gas outlet connection to patient

REF – 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

N E O P U F F ™ t e c h n i c a l m a nu a l

3

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. • The 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.

N E O P U F F ™ t e c h n i c a l m a nu a l

4

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

N E O P U F F ™ t e c h n i c a l m a nu a l

5

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

N E O P U F F ™ t e c h n i c a l m a nu a l

6

3. Service Information continued

3.3.1 Testing of the Manometer 1. Lift the cover off the Max Pressure Relief Valve slightly and turn out of the way. 2. Disconnect 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. Connect 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. With 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. Close the Peak Inspiratory Pressure valve by turning the knob fully clockwise. 3. Adjust the Max Pressure Relief knob clockwise or counterclockwise until the manometer reads 40 cmH2O. 4. Turn 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. Disconnect the F&P Neopuff™ / Perivent™ Infant Resuscitator from any other equipment. 2. Remove the opaque plastic plug in the lens of the manometer. 3. Using 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. Verify 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. Set 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. Set the gas supply to 15 L/min. Close the bleed valve and check that the gauge reads no higher than 80 cmH2O. 3. Set 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. Reset 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. Fit 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. Carry 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. Fit 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.

N E O P U F F ™ t e c h n i c a l m a nu a l

7

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:

N E O P U F F ™ t e c h n i c a l m a nu a l

8

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 #8×1” 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).

N E O P U F F ™ t e c h n i c a l m a nu a l

9

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

N E O P U F F ™ t e c h n i c a l m a nu a l

10

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

N E O P U F F ™ t e c h n i c a l m a nu a l

11

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.

N E O P U F F ™ t e c h n i c a l m a nu a l

12

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: +64 9 574 0100 Fax: +64 9 574 0158 Email: [email protected] Web: 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