FLAEM Pulmowaves P0112EM F1000 Gebrauchs- Und Wartungsanleitung Seite 2

SCHEMA DI COLLEGAMENTO PER NOMENCLATURA - CONNECTION DIAGRAM FOR NOMENCLATURE
SCHÉMA DE CONNEXION POUR NOMENCLATURE - SCHALTPLAN FÜR DIE BEZEICHNUNGEN
ESQUEMA DE CONEXIÓN PARA NOMENCLATURA - СХЕМА СОЕДИНЕНИЯ СОСТАВНЫХ ЧАСТЕЙ
SCHEMAT POŁĄCZEŃ DLA NOMENKLATURY -
A1
A9
A13
C2
C1
B2
A8
A13
B3
A7
C3
B1
A10
B
B5
A6
B6
C4
A12
C5
A11
We are pleased you have purchased our product and we thank you for your trust in us.
It is very important that the health care worker and/or the patient read and understand
INTENDED USE
Pulmowaves is a medical device is for respiratory rehabilitation physiotherapy and in particular for the removal
of tracheobronchial secretions, including a nebulising device on demand.
The Medical Device should be prepared and used in the presence of or by qualified personnel for respiratory
A2
rehabilitation physiotherapy who have read and understood this instruction manual provided, or adults who
have received specific information from the aforementioned qualified personnel and who have read and
understood this user manual provided.
The medical device can also be used for home-care treatment.
A
The recommended therapeutic session is approximately 15-20 minutes according to the doctor's assessment
and the physical condition of the patient.
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The device does not require lubrication, is manageable, simple to use, reliable, resistant and quiet.
Note: Use only original FLAEM accessories
OPERATING INSTRUCTIONS
- Drugs in solution can be nebulised with the device.
- COPD chronic obstructive pulmonary disease (Stage 0 to Stage IV in accordance with the GOLD guidelines).
- Bronchiectasis.
- Cystic Fibrosis.
- Neuromuscular, orthopedic or other disorders involving the respiratory system (bronchial hypersecretion,
ineffective cough) or who needs a quick effective removal of secretions.
CONTRAINDICATIONS FOR USE
- Drugs in suspension cannot be nebulised with the device.
- Children younger than 3 years old.
- Patients with cardiovascular instability.
A5
A4
DEVICE NOMENCLATURE
A Respiratory physiotherapy device
A1 Switch
A2 Pressure Gauge
A3 Flow regulator
A4 Pulsed air output
A5 15Vdc output power supply socket for
Ultrasonic nebuliser with Protective cap
A6 Pressure switch input
A7 Filter tube
A8 Filter
A9 Pressure switch tube
A10 Pulsed air tube
A11 Power supply socket
A12 Power supply cable
A13 Tube connector clip
B4
COMPOSITION
The M.D. is a system composed of a pneumatic compressor, an ultrasonic nebulising device used to nebulise
saline solution only, and a dispenser equipped with a PEP (Positive Expiratory Pressure) device
Pulmowaves
Device for respiratory rehabilitation physiotherapy
the device use and maintenance information.
B Ultrasonic Nebuliser Device
B1 Ultrasonic device switch
B2 Ultrasonic Nebuliser Cover
B3 Ultrasonic Nebuliser Valve
B4 Ultrasonic nebuliser power supply socket
B5 Power supply cable for ultrasonic nebuliser
device
B6 Table stand
C ACCESSORIES
C1 PEP adjustment ring
C2 Mouthpiece
C3 PEP Fitting
C4 Nose clip
C5 Valve for use without ultrasonic nebuliser
.
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THERAPY
DATE TIME
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