Important ................................................. 2
Application............................................... 3
Controls and connections ........................ 3
Installation and use..................................3
Cleaning and disposal .............................4
Technical features ...................................4
CAUTION: INDICATION OF DANGER
Attention: Important indication
General information
•
Read this manual carefully before using
the venturi nozzle
vacuum.
•
AFTER UNPACKING, CONNECT THE DEVICE
AS DESCRIBED IN THE SECTION
“INSTALLATION AND USE”.
•
BEFORE EACH USE CARR
OPERATIONS DESCRIBED
“INSTALLATION AND USE”.
•
INSTALLATIONS THAT ARE NOT ENVISAGED
BY THIS MANUAL MAY REDUCE THE SAFETY
LEVEL OF THE APPLIANCE.
•
BEFORE EACH USE, ENS
DIRECT SUCTION NOZZLE FOR HIGH FLOW /
HIGH VACUUM, IS DIRECTLY OR INDIRECTLY
CONNECTED TO A COLLE
FITTED WITH AN OVERF
ANTIBACTERIAL FILTER
CONNECTOR HOSES USED CONFORM WITH
THE STANDARD EN ISO 10079-3.
•
The company will not
accept any
responsibility if the instructions in this
manual are not observed, if original spare
parts and/or authorized technicians are
not used.
Connections
•
CONNECT THE UNIT AND CHECK THE SEALS
BETWEEN THE COMPONENTS AS DESCRIBED
IN “START-UP PROCEDURE” SECTION.
FAILURE TO MAKE THES
COMPROMISE THE SAFET
FUNCTIONING OF THE DEVICE.
•
OILS AND GREASES MUS
CONTACT WITH THE EQUIPMENT.
•
The vacuum supply connector is positioned
on the back
part of the device and may be
identified by referring to the drawing on page
3 of this manual (pos. 4).
Operation
•
THE VENTURI NOZZLE FOR HIGH FLOW / HIGH
VACUUM, MUST BE USED CAREFULLY AND ONLY
BY PERSONNEL WHO ARE
CONSEQUENCES OF THIS THERAPY.
•
Disconnect the vacuum supply when the
unit is not in use.
Service
•
All the modifications and repairs must only
be performed by personnel authorized by
the Manufacturer
or by hospital technicians
approved by the same company.
•
Original spare
parts must always be used
for the maintenance operations.
•
Check the direct suction nozzle every day
or in accordance with hospital routine.
•
For periodical updating reasons, the device
configuration can be subjected to changes.
Therefore, the Manufacturer
guarantees
spare parts to be available for at least 5
years from the manufacturing date.
•
Any modifications to the device must be
approved by the Manufacturer
, and carried
out in accordance with the procedures
prescribed.
The device has been
designed and
manufactured to satisfy the safety
requirements of the following standards:
EN ISO 10079-3
