Modification And Misuse; Essential Requirements; During Use - Nouvag Dispenser DP 30 Instrucciones De Uso

Dispenser DP 30
3.3

Modification and misuse

Modifications/manipulations on the Dispenser DP 30 and its accessories are not permitted. For
consequential complications, resulting from illicit modifications/manipulations the manufacturer assumes
no responsibility and the guarantee is void.
3.4

Essential requirements

The Dispenser DP 30 may only be
operated by qualified and trained
personnel.
The use of third-party products is the
responsibility of the operator.
Functionality and patient safety cannot be
guaranteed with third-party accessories.
Repairs may only be performed by
authorized NOUVAG service technicians.
The Dispenser DP 30 may only be operated under constant supervision of medical personnel. The
absence of a warning buzz to indicate malfunctions of the device requires the permanent control of the
volumetric displacement of the pump.
3.5

During use

The device is not sterile on delivery.
Please observe the cleaning instructions
on Chapter 8.
At choice of the instrument the user has
to make sure it confirms to EN ISO 10993,
means that it's biocompatible.
Dispenser DP 30, operating instructions, REF 31678, V52/17
Improper use or repair of the device, or failure to
observe these instructions, relieves Nouvag AG from
any obligation arising from warranty provisions or
other claims.
Prior to using the device, before startup, and before
operation, the user must always ensure that the
device and accessories are in good working order
and are clean, sterile and operational.
Ensure that the operating voltage setting
corresponds to the local mains voltage.
Do not use device in the vicinity of flammable
mixtures!
The employment of the Dispenser DP 30 other than
that for which it was designed (see chapter 1.1) is not
permitted. The responsibility is solely carried by the
operator.
EN
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