Instructions for use SONICflex rootplaner
6 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 6.1 Preparations at the site of use
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6 Reprocessing steps in accordance with ISO 17664-1 /
ISO 17664-2
NOTE
The following reprocessing procedures apply to SONICflex tips, torque wrench
and nozzle pin.
6.1 Preparations at the site of use
WARNING
Hazard from contaminated products.
Patients, users or third parties could be infected by contaminated medical
devices.
4
Take suitable personal protective measures.
WARNING
Sharp tip in the medical device.
Danger of injury from sharp tip.
4
Rev´move tip.
NOTE
Do not place the tips in the drill bit bath since, otherwise, the fine capillaries
can no longer be rinsed under running water leading to strong corrosion.
4
To minimise the risk of infection during reprocessing, always wear protect-
ive gloves.
4
Reprocess the medical device right after treatment.
4
Remove all residual cement, composite or blood immediately.
4
Wipe-disinfect the medical device before transport.
4
Remove the tip from the medical device.
4
Do not place in solutions or similar substances.
CAUTION
Never reprocess the medical device with chloride-containing products.
Malfunction and material damage.
4
Reprocess it in a washer disinfector only.
KaVo recommends the following products based on the compatibility of the ma-
terials. The microbiological efficacy must be ensured by the disinfectant manu-
facturer and proven by an expert opinion.
▪ CaviWipes and CaviCide made by Metrex
▪ Mikrozid AF made by Schülke & Mayr (Liquid or wipes)
▪ FD 322 made by Dürr
Consumables required:
▪ Cloths for wiping the medical device.
4
Spray the disinfectant on a cloth, then wipe down the medical device and al-
low the disinfectant to act according to the instructions of the disinfectant
manufacturer.
4
Follow the instructions for use of the disinfectant.
6.2 Manual Reprocessing
This product is not designed for manual internal and external cleaning and
manual internal and external disinfection.
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