Reprocessing Steps In Accordance With Iso 17664-1 / Iso 17664-2; Preparations At The Site Of Use; Manual Reprocessing - KaVo MULTIflex LED coupling 460 LED Instructions For Use Manual

Instructions for use MULTIflex LED coupling 460 LED - 1.007.3201
7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.1 Preparations at the site of use
7 Reprocessing steps in accordance with ISO 17664-1 /
ISO 17664-2

7.1 Preparations at the site of use

Hazard from contaminated products.
Contaminated products are associated with an infection hazard.
4 Take suitable personal protective measures.
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 instrument from the medical device.
4 Do not place in solutions or similar substances.
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.
Approved disinfectants:
▪ 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.

7.2 Manual Reprocessing

This product is not designed for manual internal and external cleaning and
manual internal and external disinfection.
For effective reprocessing, automated internal and external cleaning as well as
automated internal and external disinfection with a cleaning and disinfection
unit in accordance with EN ISO 15883-1 is required.
Never reprocess this medical device in an ultrasonic cleaner.
Malfunction and material damage.
4 Reprocess it in a washer disinfector only.
WARNING
CAUTION
CAUTION
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