Dentsply Sirona Cavitron G139 Mode D'emploi page 6

• It is the responsibility of the dental healthcare
professional to determine the appropriate uses of
this product and to understand:
• the health of each patient,
• the dental procedures being undertaken,
• applicable industry and governmental agency
recommendations for infection control in
dental healthcare settings,
• requirements and regulations for safe
practice of dentistry, and
• these Directions for Use in their entirety,
including Section 4 Precautions, Section 7
Infection Control, and Section 11 System Care.
• This product is designed to assist in eliminating
susceptibility to retraction of oral fluids. To ensure
adequate protection from cross-contamination
from other devices connected to the dental unit,
it is highly recommended that the dental unit be
installed with anti-retraction features. Additionally,
the dental unit, including the anti-retraction
features, must be properly maintained and
periodically tested. For more information, please
contact your dental unit manufacturer.
• Where asepsis is required or deemed appropriate
in the best professional judgment of the dental
healthcare professional, this product should not be
used.
• During boil-water advisories, this product should
not be operated as an open water system (e.g.
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connected to a public water system). Dental
healthcare professionals should discontinue use
on patients and contact the local water authority
to determine when it is safe to continue use of
this product. When the advisory is cancelled, the
local water authority should provide guidance
for flushing of waterlines. All incoming waterlines
from the public water system inside the dental
office (e.g., faucets, waterlines, and dental
equipment) should be flushed in accordance with
manufacturer's instructions for a minimum of 5
minutes.
• Prior to beginning treatment, patients should rinse
with a known antimicrobial such as Chlorhexidine
Gluconate 0.12%. Rinsing with an antimicrobial
reduces the chance of infection and reduces the
number of microorganisms released in the form of
aerosols during treatment.
• The use of high volume saliva evacuation (HVE)
to reduce the quantity of aerosols released during
treatment is highly recommended.
• Failure to follow recommendations for
environmental operating conditions, including input
water temperature, could result in injury to patients
or users.
• Handle Cavitron insert with care. Improper handling
of insert, specifically the insert tip, may result in
injury and/or cross contamination.
• Failure to follow properly validated sterilization
processes and approved aseptic techniques for
Cavitron inserts may result in cross contamination.
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