ResMed AirFit F20 Manuel utilisateur

User guide

Full face mask

User guide

English | Français

Español | Português

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76

Fitting / Mise en place / Colocación / Colocação

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Adjustment / Ajustement / Ajuste / Ajuste

Removal / Retrait / Remoción / Remoção

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Disassembly / Démontage / Desensamblado /

Desmontagem

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Reassembly / Remontage / Reensamblado / Remontagem

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Cleaning the vent / Nettoyage de l’oriﬁce de ventilation

/ Limpieza del oriﬁcio de ventilación / Limpeza do

respiradouro

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English 1

ENGLISH

Full face mask

Thank you for choosing the AirFit F20. This document provides the user

instructions for the AirFit F20 and AirFit F20 for Her masks referred to

collectively as AirFit F20 throughout this manual.

Using this guide

Please read the entire guide before use. When following instructions,

refer to the images at the front of the guide.

Intended use

The AirFit F20 is a non-invasive accessory used for channeling airflow

(with or without supplemental oxygen) to a patient from a positive airway

pressure (PAP) device such as a continuous positive airway pressure

(CPAP) or bilevel system.

The AirFit F20 is:

• to be used by patients weighing more than 66 lb (30 kg) for whom

positive airway pressure therapy has been prescribed

• intended for single-patient reuse in the home environment and multi-

patient reuse in the hospital/institutional environment.

WARNING

Magnets are used in the lower headgear straps and the frame of the

AirFit F20. Ensure the headgear and frame is kept at least 2" (50 mm)

away from any active medical implant (eg, pacemaker or

defibrillator) to avoid possible effects from localized magnetic fields.

The magnetic field strength is less than 400 mT.

Contraindications

Use of masks with magnetic components is contraindicated in patients

with the following pre-existing conditions:

• a metallic hemostatic clip implanted in your head to repair an

aneurysm

• metallic splinters in one or both eyes following a penetrating eye

injury.

2

GENERAL WARNINGS

• The mask must be used under qualified supervision for users who

are unable to remove the mask by themselves. The mask may not

be suitable for those predisposed to aspiration.

• The mask must be fitted with the supplied elbow (containing the

valve and vent assembly) to ensure safe and functional usage

unless otherwise specified. Do not use the mask if the valve or

vent assembly is damaged or missing.

• The elbow, valve and vent assembly have specific safety

functions. The mask should not be worn if the valve is damaged

as it will not be able to perform its safety function. The elbow

should be replaced if the valve is damaged, distorted or torn. The

vent holes and valve should be kept clear.

• The mask should only be used with CPAP or bilevel devices

recommended by a physician or respiratory therapist.

• Avoid connecting flexible PVC products (eg, PVC tubing) directly

to any part of the mask. Flexible PVC contains elements that can

be damaging to the materials of the mask, and may cause the

components to crack or break.

• The mask should not be used unless the device is turned on. Once

the mask is fitted, ensure the device is blowing air.

Explanation: CPAP and bilevel devices are intended to be used

with special masks (or connectors) which have venting to allow

continuous flow of air out of the mask. When the device is turned

on and functioning properly, new air from the device flushes the

exhaled air out through the mask holes. When the device is

turned off, the mask valve opens to atmosphere allowing fresh air

to be breathed. However, a higher level of exhaled air may be

rebreathed when the device is off. This applies to most full face

masks for use with CPAP and bilevel devices.

• Follow all precautions when using supplemental oxygen.

• Oxygen flow must be turned off when the CPAP or bilevel device

is not operating, so that unused oxygen does not accumulate

within the device enclosure and create a risk of fire.

• Oxygen supports combustion. Oxygen must not be used while

smoking or in the presence of an open flame. Only use oxygen in

well ventilated rooms.

English 3

• At a fixed rate of supplemental oxygen flow, the inhaled oxygen

concentration varies, depending on the pressure settings, patient

breathing pattern, mask, point of application and leak rate. This

warning applies to most types of CPAP or bilevel devices.

• The technical specifications of the mask are provided for your

clinician to check that they are compatible with the CPAP or

bilevel device. If used outside specification or if used with

incompatible devices, the seal and comfort of the mask may not

be effective, optimum therapy may not be achieved, and leak, or

variation in the rate of leak, may affect the CPAP or bilevel device

function.

• Discontinue using this mask if you have ANY adverse reaction to

the use of the mask, and consult your physician or sleep therapist.

• Using a mask may cause tooth, gum or jaw soreness or aggravate

an existing dental condition. If symptoms occur, consult your

physician or dentist.

• The F20 line of full face CPAP masks are not intended to be used

simultaneously with nebulizer medications that are in the air path

of the mask/tube.

• As with all masks, some rebreathing may occur at low CPAP

pressures.

• Refer to your CPAP or bilevel device manual for details on

settings and operational information.

• Remove all packaging before using the mask.

Using your mask

When using your mask with ResMed CPAP or bilevel devices that have

mask setting options, refer to the Technical specifications section in this

user guide for the correct setting.

For a full list of compatible devices for this mask, see the Mask/Device

Compatibility List on www.resmed.com/downloads/masks. If you do not

have internet access, please contact your ResMed representative.

Use a standard conical connector if pressure readings and/or

supplemental oxygen are required.

4

Fitting

1. Twist and pull both magnetic clips away from the frame.

2. Ensure that the ResMed logo on the headgear is facing outwards and

is upright. With both lower headgear straps released, hold the mask

against your face and pull the headgear over your head.

3. Bring the lower straps below your ears, and attach the magnetic clip

to the frame.

4. Undo the fastening tabs on the upper headgear straps. Pull the straps

evenly until the mask is stable and positioned as shown in the

illustration. Reattach the fastening tabs.

5. Undo the fastening tabs on the lower headgear straps. Pull the straps

evenly until the mask is stable and sits comfortably on the chin.

Reattach the fastening tabs.

6. Connect the device air tubing to the elbow. Attach the elbow to the

mask by pressing the side buttons and pushing the elbow into the

mask, ensuring it clicks in on both sides.

7. Your mask and headgear should be positioned as shown in the

illustration.

Adjustment

If necessary, slightly adjust the position of the mask for the most

comfortable fit. Ensure that the cushion is not creased and the headgear

is not twisted.

1. Turn on your device so that it is blowing air.

Adjustment tips:

 With air pressure applied, pull the mask away from your face to

allow the cushion to inflate and reposition onto your face.

 To resolve any leaks at the upper part of the mask, adjust the

upper headgear straps. For the lower part, adjust the lower

headgear straps.

 Adjust only enough for a comfortable seal. Do not overtighten as

this may cause discomfort.

Removal

1. Twist and pull both magnetic clips away from the frame.

2. Pull the mask away from your face and back over your head.

English 5

Disassembly

If the mask is connected to your device, disconnect the device air tubing

from the elbow.

1. Undo the fastening tabs on the upper headgear straps. Pull the straps

out of the frame.

Tip: Keep the magnetic clips attached to the lower headgear straps to

easily distinguish the upper and lower straps when reassembling.

2. Remove the elbow from the mask by pressing the side buttons and

pulling the elbow away.

3. Hold the side of the frame between the upper and lower arms. Gently

pull the cushion away from the frame.

Reassembly

1. Attach the cushion to the frame by aligning the circular openings and

pushing together until retained.

2. With the ResMed logo on the headgear facing outside and upright,

thread the upper headgear straps into the frame slots from the inside.

Fold them over to secure.

Cleaning your mask at home

Handwash your mask and headgear by gently rubbing in warm

(approximately 86°F/30°C) water using mild liquid detergent. Rinse all

components well under running water and allow to air dry out of direct

sunlight.

WARNING

• As part of good hygiene, always follow cleaning instructions and

use a mild liquid detergent. Some cleaning products may damage

the mask, its parts and their function, or leave harmful residual

vapours that could be inhaled if not rinsed thoroughly.

• Regularly clean your mask and its components to maintain the

quality of your mask and to prevent the growth of germs that can

adversely affect your health.

6

CAUTION

Visible criteria for product inspection: If any visible deterioration of a

system component is apparent (cracking, discoloration, tears etc.),

the component should be discarded and replaced.

Daily/After each use:

1. Disassemble the mask according to the disassembly instructions.

2. Rinse the frame, elbow and cushion under running water. Clean with a

soft brush until dirt is removed.

3. Soak the components in warm water with a mild liquid detergent for

up to ten minutes.

4. Shake the components in the water.

5. Brush the moving parts of the elbow and around the vent holes.

6. Brush the areas of the frame where the arms connect, and inside and

outside the frame where the elbow connects.

7. Rinse the components under running water.

8. Leave the components to air dry out of direct sunlight. Make sure to

squeeze the arms of the frame to ensure that excess water is

removed.

Weekly:

1. Disassemble the mask. The magnets can remain attached to the

headgear during cleaning.

2. Handwash the headgear in warm water with mild liquid detergent.

3. Rinse the headgear under running water. Inspect to ensure the

headgear is clean and detergent free. Wash and rinse again, if

necessary.

4. Squeeze the headgear to remove excess water.

5. Leave the headgear to air dry out of direct sunlight.

Reprocessing the mask between patients

Only Sleep Lab Mask (SLM) variants of the mask are intended for multi-

patient re-use. When using between patients, these masks must be

reprocessed according to cleaning and disinfection instructions available

on ResMed.com/downloads/masks.

English 7

Troubleshooting

Problem/possible cause

Solution

Mask is uncomfortable.

Headgear straps are too tight. The cushion membrane is designed to inflate

against your face to provide a comfortable

seal with low headgear tension. Adjust straps

evenly. Ensure that the headgear straps are

not too tight and that the cushion is not

creased.

Mask could be the wrong size. Talk to your clinician to have your face size

checked against AirFit F20 fitting template.

Note that sizing across different masks is not

always the same.

Mask is too noisy.

Elbow incorrectly installed or incorrect

assembly of the mask system.

Remove the elbow from your mask, then

reassemble according to the instructions.

Check that the mask is correctly assembled

according to the instructions.

Vent is dirty. Use a soft bristle brush to clean the vent.

Mask leaks around the face.

Cushion membrane is creased. Mask is

incorrectly positioned or adjusted.

Refit your mask according to the instructions.

Ensure that you position the cushion correctly

on your face before pulling headgear over

your head. Do not slide the mask down your

face during fitting as this may lead to

creasing of the cushion.

Mask could be the wrong size. Talk to your clinician to have your face size

checked against fitting template. Note that

sizing across different masks is not always

the same.

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Technical specifications

Pressure-flow curve

The mask contains passive venting to protect

against rebreathing. As a result of manufacturing

variations, the vent flow rate may vary.

Pressure

(cm H

2

O)

Flow

(L/min)

3

19

8

32

10

37

12

41

16

48

20

54

24

60

28

66

30

69

32

72

36

77

40

82

Dead space

information

Physical dead space is the empty volume of the mask to the end

of the swivel. Using the large cushions it is 240 mL.

Therapy pressure

3 to 40 cm H

2

O

Resistance with

Anti Asphyxia Valve

(AAV) closed to

atmosphere

Drop in pressure measured (nominal)

at 50 L/min: 0.2 cm H

2

O

at 100 L/min: 0.6 cm H

2

O

Inspiratory and

expiratory

resistance with Anti

Asphyxia Valve

(AAV) open to

atmosphere

Inspiration at 50 L/min:

0.6 cm H

2

O

Expiration at 50 L/min:

0.7 cm H

2

O

English 9

Anti Asphyxia Valve

(AAV) open-to-

atmosphere

pressure

≤3 cm H

2

O

Anti Asphyxia Valve

(AAV) closed-to-

atmosphere

pressure

≤3 cm H

2

O

Environmental

conditions

Operating temperature: 41°F to 104°F (5°C to 40°C)

Operating humidity: 15% to 95% non-condensing

Storage and transport temperature: -4°F to 140°F (-20°C to +60°C)

Storage and transport humidity: up to 95% non-condensing

Sound

DECLARED DUAL-NUMBER NOISE EMISSION VALUES in

accordance with ISO 4871. The A-weighted sound power level of

the mask is 30 dBA, with uncertainty of 3 dBA. The A-weighted

sound pressure level of the mask at a distance of 1 m is 23 dBA,

with uncertainty of 3 dBA.

Gross dimensions

Mask fully assembled with elbow assembly (no headgear)

6.1" (H) x 6.3" (W) x 5.8" (D)

(154 mm (H) x 159 mm (W) x 147 mm (D))

International

Commission on

Non-Ionizing

Radiation

Protection (ICNIRP)

Magnets used in this mask are within ICNIRP guidelines for

general public use.

Service life

The service life of the AirFit F20 mask system is dependent on the

intensity of usage, maintenance, and environmental conditions to

which the mask is used or stored. As this mask system and its

components are modular in nature, it is recommended that the

user maintain and inspect it on a regular basis, and replace the

mask system or any components if deemed necessary or

according to the ‘visual criteria for product inspection’ in the

‘Cleaning your mask at home’ section of this guide. Refer to the

‘Mask components’ section of this guide for information of how to

order replacement parts.

10

Mask setting options

For AirSense, AirCurve or S9: Select 'Full Face'.

For other devices: Select 'MIR FULL' (if available), otherwise

select 'FULL FACE' as the mask option.

Notes:

• This product is not made with PVC or phthalates such as DEHP, DBP

or BBP.

• This product is not made with natural rubber latex.

• The manufacturer reserves the right to change these specifications

without notice.

Storage

Ensure that the mask is thoroughly clean and dry before storing it for any

length of time. Store the mask in a dry place out of direct sunlight.

Disposal

This mask does not contain any hazardous substances and may be

disposed of with your normal household refuse.

English 11

Symbols

The following symbols may appear on your product or packaging:

Catalog number

Batch code

Humidity limitation

Temperature limitation

Fragile, handle with care

Not made with natural rubber

latex

Manufacturer

European Authorized

Representative

Keep away from rain

This way up

Full face mask

Device setting - Full Face

Size - small

Size - medium

Size - large

Indicates a Warning or Caution and alerts you to a possible injury or explains

special measures for the safe and effective use of the device

Caution, consult accompanying documents

Prescription only (In the US, Federal law restricts these devices to sale by or on

the order of a physician)

Limited warranty

ResMed Pty Ltd (ResMed) warrants that your ResMed mask system

(including mask frame, cushion, headgear and tubing) will be free from

defects in material and workmanship from the date of purchase for 90

days, or in the case of disposable masks and disposable mask

components for 7 days. This warranty is only available to the initial

consumer. It is not transferable. If the product fails under conditions of

normal use, ResMed will repair or replace, at its option, the defective

product or any of its components. This limited warranty does not cover: a)

any damage caused as a result of improper use, abuse, modification or

alteration of the product; b) repairs carried out by any service organization

that has not been expressly authorized by ResMed to perform such

repairs; and c) any damage or contamination due to cigarette, pipe, cigar

or other smoke. Warranty is void on product sold, or resold, outside the

region of original purchase.

Warranty claims on defective product must be made by the initial

consumer at the point of purchase.

This warranty replaces all other expressed or implied warranties, including

any implied warranty of merchantability or fitness for a particular purpose.

Some regions or states do not allow limitations on how long an implied

warranty lasts, so the above limitation may not apply to you.

ResMed will not be responsible for any incidental or consequential

damages claimed to have resulted from the sale, installation or use of any

ResMed product. Some regions or states do not allow the exclusion or

limitation of incidental or consequential damages, so the above limitation

may not apply to you. This warranty gives you specific legal rights, and

you may also have other rights which vary from region to region. For

further information on your warranty rights, contact your local ResMed

dealer or ResMed office.

12

Français 1

FRANÇAIS

Masque facial

Merci d'avoir choisi l'AirFit F20. Ce document indique comment utiliser

les masques AirFit F20 et AirFit F20 for Her, désignés par AirFit F20 dans

le présent manuel.

Utilisation de ce guide

Veuillez lire le guide entièrement avant d’utiliser ce masque. Les

instructions doivent être lues en consultant les illustrations au début de

ce manuel.

Usage prévu

L'appareil AirFit F20 est un accessoire non invasif utilisé pour acheminer

au patient le débit d'air (avec ou sans adjonction d'oxygène) produit par

un appareil à pression positive tel qu'un appareil de PPC ou à deux

niveaux de pression.

L'AirFit F20 est prévu pour :

• une utilisation par des patients pesant plus de 66 lb (30 kg) à qui un

traitement par pression positive a été prescrit;

• un usage multiple par un seul patient à domicile ou un usage multiple

par plusieurs patients en milieu médical.

AVERTISSEMENT

Des aimants sont utilisés dans les sangles inférieures du harnais et

dans l'entourage rigide de l'AirFit F20. Vérifiez que le harnais et

l'entourage rigide soient maintenus à une distance minimale de

50 mm (2 pouces) de tout implant médical actif (p. ex. un pacemaker

ou un défribillateur) pour éviter les effets possibles des champs

magnétiques localisés. La force du champ magnétique est inférieure

à 400 mT.

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Contre-indications

L'utilisation des masques avec des composants magnétiques est contre-

indiqué chez les patients présentant les caractéristiques pré-existantes

suivantes :

• dispositif hémostatique métallique implanté dans le crâne suite à un

anévrisme;

• éclats métalliques dans un œil ou dans les deux yeux suite à un

traumatisme oculaire pénétrant.

AVERTISSEMENTS D’ORDRE GÉNÉRAL

• Le masque doit être utilisé sous le contrôle d'une personne

qualifiée si le patient n'est pas en mesure de l'enlever de lui-

même. Le masque peut ne pas convenir aux patients sujets aux

aspirations trachéo-bronchiques.

• Le masque doit être équipé du coude qui l'accompagne (et

contenant la valve et l'orifice de ventilation) afin d'assurer une

utilisation sûre et pratique, sauf si autrement spécifié. Ne pas

utiliser le masque si la valve ou l'orifice de ventilation sont

endommagés ou manquants.

• L’ensemble coude, valve et orifice de ventilation possède des

caractéristiques de sécurité spécifiques. Le masque ne doit pas

être porté si la valve est endommagée, auquel cas elle n'est pas

en mesure de remplir sa fonction de sécurité. Le coude doit être

remplacé si la valve est endommagée, déformée ou déchirée. Les

orifices de ventilation et la valve ne doivent jamais être obstrués.

• Le masque doit être utilisé uniquement avec les appareils de PPC

ou à deux niveaux de pression recommandés par un médecin ou

un kinésithérapeute respiratoire.

• Éviter de raccorder des produits en PVC souple (par ex. un circuit

en PVC) directement aux composants de ce masque. Le PVC

souple contient des éléments qui peuvent endommager les

matériaux du masque et entraîner leur fissuration ou leur rupture.

• Le masque ne doit être porté que si l'appareil est sous tension.

Une fois le masque en place, s'assurer que l'appareil produit un

débit d'air.

Explication : Les appareils de PPC et à deux niveaux de pression

sont conçus pour une utilisation avec des masques (ou raccords)

spéciaux possédant des orifices de ventilation qui permettent

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