Instructions for use INTRAflex LUX 2 Programm 2307 LN - 0.535.6190, 2320 LN - 0.535.6180, 2325 LN -
0.535.6210
7 Reprocessing steps in accordance with ISO 17664 | 7.3 Automated reprocessing
7.2.3 Manual disinfection - external
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
Malfunctioning from using a disinfectant bath or chloride-containing
disinfectants.
Defects in the device.
▶
Disinfect manually only!
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:
▪ CaviWipes and 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.
7.2.4 Manual disinfection - internal
Not applicable.
The interior of this product is not designed for manual disinfection.
7.3 Automated reprocessing
Not applicable. Do not wash the product in thermodisinfectants.
7.4 Care products and systems - Servicing
WARNING
Sharp tool in the medical device.
Injury hazard from sharp and/or pointed tool.
▶
Remove the tool.
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Summary of Contents for INTRAFLEX LUX 2 2307 LN
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