ARJO HUNTLEIGH Maxi Air Bedienungsanleitung

Maxi Air

Instructions for Use

...with people in mind

001-35001-EN Rev 3 • 06/2017

Design Policy and Copyright

® and ™ are trademarks belonging to the ArjoHuntleigh group of companies.

As our policy is one of continuous improvement, we reserve the right to modify designs without

prior notice. The content of this publication may not be copied either whole or in part without the

consent of ArjoHuntleigh AB.

WARNING

To avoid injury, always read this Instructions for Use and accompanying documents before using

the product.

It is mandatory to read the Instructions for Use.

Table of Contents iii

Table of Contents

Foreword .................................................................................................................................. 1

Intended Use ........................................................................................................................... 2

Safety Instructions ................................................................................................................. 3

Preparations ............................................................................................................................ 4

Product Speciﬁ cations ........................................................................................................... 5

Parts Designation ................................................................................................................... 6

Product Description/Functions ............................................................................................. 7

Correct Placement of the Patient .......................................................................................... 8

Correct Placement of the Maxi Air air supply ...................................................................... 9

Transfer ................................................................................................................................. 10

Disinfection Instructions ..................................................................................................... 14

Care and Preventive Maintenance ...................................................................................... 16

Troubleshooting ................................................................................................................... 18

Technical Speciﬁ cations ...................................................................................................... 19

Labels on Maxi Air mattress ................................................................................................ 22

Labels on Maxi Air air supply .............................................................................................. 23

Approvals and List of Standards ........................................................................................ 24

Electromagnetic Compatibility ............................................................................................. 25

Parts and Accessories .......................................................................................................... 28

Intentionally left blank

Foreword 1

Thank you for purchasing

ArjoHuntleigh equipment.

Your Maxi Air™ is a part of a series of quality

products designed for patient transfers,

especially for hospital and professional

healthcare facilities.

Please contact us if you have any questions

about the operation or maintenance of your

ArjoHuntleigh equipment.

Please read this Instructions for Use

thoroughly!

Please read this Instructions for Use (IFU) in its

entirety before using your Maxi Air. Information

in this IFU is crucial to the proper operation and

maintenance of the equipment. It will help to

protect your product, and make sure that the

equipment performs to your satisfaction. The

information in this IFU is important for your

safety and must be read and understood to help

prevent possible injuries.

Unauthorized modiﬁ cations on any

ArjoHuntleigh equipment can aﬀ ect its safety.

ArjoHuntleigh will not be held responsible for

any accidents, incidents or lack of performance

that occur as a result of any unauthorized

modiﬁ cation to its products.

Service and Support

A service routine must be performed on your

Maxi Air every year by qualiﬁ ed personnel to

ensure the safety and operating procedures of

your product. See section, “Care and Preventive

Maintenance”.

If you require further information, please contact

ArjoHuntleigh for comprehensive support and

service programs to maximize the long-term

safety, reliability and value of the product.

Contact your local ArjoHuntleigh representative

for replacement parts. The telephone numbers

appear on the last page of this IFU.

Manufacturer Information

This product was manufactured by:

ArjoHuntleigh AB

Hans Michelsensgatan 10

211 20 Malmö

SWEDEN



Deﬁ nitions Used in this Manual

WARNING:

Means: Failure to understand and follow this

instruction may result in injury to yourself and

others.

CAUTION:

Means: Failure to follow this instruction may

cause damage to the product(s).

NOTE:

Means: Important information regarding correct

use of the product.

Means: The name and address of the

manufacturer.

Means: Read the Instructions for use

Foreword

Intended Use

This equipment should only be used for the

purpose speciﬁ ed in this Instructions for

Use (IFU). Any other use is prohibited.

The Maxi Air is intended for lateral transfer or

repositioning of hospital and professional

healthcare facility patients. The equipment must

be used under the supervision of trained

caregivers with adequate knowledge of the care

environment, its common practices and

procedures, and in accordance with the

guidelines in this Instructions for Use (IFU).

The equipment must only be used for the

purposes stated above, and removable parts

must be mounted according to the

recommendations given in this IFU.

The System

The Maxi Air (air supply and mattress) is an air

assisted lateral patient transfer system for use in

lateral transfers and repositioning.

Patient Assessment

It is recommended that facilities establish

regular assessment routines. Caregivers must

assess each patient according to the following

criteria prior to use:

• This equipment is intended for patients

who are dependent, unable or not

required to participate in the transfer

activity.

• The equipment is intended for adult

patients.

• The patient safe working load (SWL) of the

MaxiAir mattress is 1200 lb / 544 kg.

• The weight, girth and body shape of the

patient should be assessed in terms of

the potential risk for the caregivers who

are to perform the patient transfer using

this equipment.

• Maxi Air is intended for use in hospital

and professional healthcare facilities.

If the patient does not meet these criteria, an

alternative equipment/system must be used.

Contraindications

This equipment can be unsuitable for patients

with thoracic, cervical or lumbar fractures. The

equipment can be unsuitable for patients whose

body shape is such that they do not comfortably

ﬁ t between the boundaries of the mattress.

Always make a clinical assessment to make

sure that the patient is suitable for the

equipment.

Expected Lifetime

The expected lifetime of the Maxi Air air supply,

is unless otherwise stated ﬁ ve (5) years, if

subject to preventive maintenance being carried

out in accordance with the instructions for “Care

and Preventive Maintenance” found in this IFU.

The expected lifetime of the Maxi Air mattress,

is twenty (20) transfers.

Intended Use

Safety Instructions 3

Safety Instructions

WARNING

Do NOT use the equipment for any type of

lifting of patients.

WARNING

Do NOT use the equipment if the power cord

is damaged. A damaged power cord may

cause serious injury to the patient and the

caregivers.

WARNING

To avoid explosion or ﬁ re, never use the

equipment in oxygen rich environment, in

presence of heat source or ﬂ ammable

anaesthetic gases.

WARNING

This equipment does not contain any HEPA-

ﬁ lter. This may cause problems for patients

sensitive to contaminated air.

WARNING

To avoid bodily injuries to the patient, use the

Maxi Air in an environment where the

temperature is below 32 °C (90 °F).

Temperatures above 32 °C (90 °F) can cause

the Maxi Air mattress surface to reach a

temperature higher than 44 °C (111 °F).

Preparations

Actions Before First Use (8 Steps)

1) Visually inspect the Maxi Air system for

damage.

2) Check that all parts are supplied. Compare

with section Parts Designation in this IFU. If

any part is missing or damaged - do NOT

use the product!

3) Read the IFU.

4) Disinfect the Maxi Air air supply. See

Disinfection Instructions section.

5) Perform a functionality test. See Care and

Preventive Maintenance section.

6) Find a good ventilated dry area for storing

the Maxi Air.

7) Choose a designated area where the IFU

should be kept, accessible at all times.

8) Make sure to have a rescue plan ready in

case of a patient emergency.

Below is the direction of the Maxi Air

mattress:

Head end

Foot end

RightLeft

Actions Before Every New Patient (6

Steps)

1) Select a suitable Maxi Air mattress size

according to sections “Correct Placement of

the Patient” and “Product Speciﬁ cations”.

Check that all parts of the Maxi Air is in place.

Compare with the section Parts Designation in

this IFU.

2) Carry out a thorough inspection for any

damage.

3) If any part is missing or damaged - do NOT

use the product!

4) Insert the patient name and date on the

Maxi Air mattress label. See Labels on the

Maxi Air Mattress section.

WARNING

To prevent cross-contamination:

• Never assign the usage of a mattress

to more than one patient.

• Always follow the disinfection

instructions in this Instructions for Use.

Make sure the Maxi Air air supply is disinfected

according to Disinfection Instructions section.

Actions Before Every Transfer (with

same patient)

1) Check that all parts are in place. Compare

with the Parts Designation in this IFU.

2) Carry out a thorough inspection for any

damage.

3) If any part is missing or damaged - do NOT

use the product!

NOTE

If you have any questions, please contact

your local ArjoHuntleigh representative for

support and service. The contact information

(ArjoHuntleigh addresses) is listed on the last

page of this IFU.

Preparations

Product Speciﬁcations 5

Maxi Air air supply

Dimensions: 12,5 x 7 x 7”(317,5 x 178 x 178 mm)

Weight: 11 lb (5 kg)

Material: ABS Plastic

Air Hose Lengths: 78” (1980 mm), 300” (7620 mm) Optional

Power Cord Length: 180” (4570 mm)

Maxi Air mattress

Widths: L 34” (860 mm), XL 39” (990 mm) and XXL 50” (1270 mm)

Length: 78” (1980 mm)

Material: Non-woven top, nylon back

L (Green handles) XL (Blue handles) XXL (Orange handles)

Product Speciﬁ cations

Parts Designation

16 8

Maxi Air air supply Maxi Air mattress

1) Carrying handle

2) Attachment hooks

3) Socket inlet

4) Push button (On/Oﬀ )

5) LED mains power indicator

6) Rubber bumper

7) Cover

8) Air ﬁ lter (inside)

9) Air hose

10) Socket

11) Snap lock button (air hose)

12) Nozzle

13) Power cord (Mains disconnection device)

14) Connection points

15) Velcro lip

16) Snap lock button

17) Safety belts

18) Transfer handles

Parts Designation

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