Instructions for use PROPHYflex 4
7 Reprocessing steps in accordance with ISO 17664 | 7.3 Manual Reprocessing
7.3.2 Manual internal cleaning
Manual internal cleaning of the PROPHYflex 4 is not applicable. For effective re-
processing, the inside of the device must be subjected to automated cleaning in
a cleaning and disinfection unit in accordance with ISO 15883-1.
7.3.3 Manual external disinfection
WARNING
Incomplete disinfection.
Infection hazard.
▶ Only use disinfection procedures that are verified to be bactericidal, fungi-
cidal and virucidal.
▶ If the disinfectants used do not meet these requirements, the process must
be concluded by disinfection of the unit(s) without packaging using a steam
steriliser.
NOTICE
Never disinfect the handpiece with chloride-containing products.
Malfunction and material damage.
▶ Only disinfect in a washer disinfector or manually.
KaVo recommends the following products based on compatibility of the materi-
als. The microbiological efficacy must be ensured by the disinfectant manufac-
turer and proven by an expert opinion.
Approved disinfectants:
▪ Mikrozid AF made by Schülke & Mayr (liquid or cloths)
▪ FD 322 made by Dürr
▪ CaviCide made by Metrex
Consumables required:
▪ Cloths for wiping the medical device.
▶ Spray the disinfectant on a cloth, then wipe down the medical device and
allow the disinfectant to act according to the instructions of the
disinfectant manufacturer.
▶ Follow the instructions for use of the disinfectant.
7.3.4 Manual internal disinfection
Manual internal disinfection of the PROPHYflex 4 is not applicable. For effective
reprocessing, the inside of the device must be subjected to automated cleaning
in a cleaning and disinfection unit in accordance with ISO 15883-1.
7.3.5 Manual drying
Manual drying of the PROPHYflex 4 is not applicable. For effective reprocessing,
the inside of the device must be subjected to automated cleaning in a cleaning
and disinfection unit in accordance with ISO 15883-1.
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