FLAEM PRO LINE PulmoWaves 2 Instrucciones Para El Uso página 15

• The Manufacturer must be contacted to report problems and/or unexpected events related to operation.
• No maintenance and/or repairs must be carried out while the device is in use.
• The Manufacturer, the Vendor and the Importer shall be held responsible for safety, reliability and performance
only if: a) the device is used in compliance with the instructions for use; b) the wiring where the device is being
used is in compliance with safety regulations and current laws.
• The Manufacturer must be contacted to report problems and/or unexpected events related to operation.
• The manufacturer must be contacted about any problems and/or unexpected events concerning operation and
for any clarifications on use, maintenance or cleaning.
• The amount of time required to switch from preservation to operating conditions is approximately 2 hours
• The components (A7, A9, A10, C1, C2, C3, C4, C5) are for personal use and should be cleaned before each use, as
described in the "Cleaning, sanitation, disinfecting and sterilising" section.
• Interactions: the materials used in contact with medications have been tested with a vast range of medications.
However, in view of the variety and continuous evolution of medications, interactions cannot be ruled out. We
recommend the medication is used as soon as possible after opening and its prolonged exposure to the nebu-
liser is avoided. The materials used in the medical device are biocompatible in accordance with the provisions
of Directive 93/42 EC as amended. However, the possibility of occurrence of allergic reactions cannot be entirely
ruled out.
• Should your device fail to perform as expected, contact the authorised service centre for clarifications.
• The supplied cable is fitted with a protective gasket (A14) to prevent the penetration of liquids into the device.
Do not separate this gasket from the cable.
INSTRUCTIONS FOR USE
Before each utilisation, wash your hands accurately and clean the device as described in the pargraph
"CLEANING, SANITISATION, DISINFECTION AND STERILISATION (for hospital use)". The parts (A7-A9-A10-
C2-C3) are for personal use only to avoid potential risks of transmitting infection. It is recommended to re-
place them every six months.
1. Insert power supply cord (A12) into socket (A11) and then connect it to a mains outlet adequate to the device
voltage. The position of the socket must be such that the device can be easily unplugged from the mains network.
B5
A10
A8
A7
A6
A4
A5
C2
C3
Tube assembly
- Connect tube (A10) to the pulsed air outlet (A4) and tube (A7)
to the pressure switch inlet (A6).
- Insert the plug (B5) of the cable (B4) into the socket (A5).
- Screw the ring nut by turning it clockwise.
- Connect the filter (A8) to the tube (A7).
WARNING
The protection cap of the 12Vdc socket must be removed to in-
sert the plug and must be replaced after use to protect the sock-
et.
Mouthpiece
A9
- Connect mouthpiece (C2) to PEP connector (C3).
- Connect the two tubes (A9-A10) coming out of (A4-A8) to PEP
connector C3.
A8
A10
C2
14