KaVo DIAGNOdent 2191, Инструкция по эксплуатации

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Instructions for use DIAGNOdent display 2191
7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.1 Preparations at the site of use
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7 Reprocessing steps in accordance with ISO 17664-1 /
ISO 17664-2
7.1 Preparations at the site of use
WARNING
Hazard from contaminated products.
Contaminated products are associated with an infection hazard.
4
Take suitable personal protective measures.
4
Turn the device off.
4
To minimise the risk of infection during reprocessing, always wear protect-
ive gloves.
4 Reprocess the medical device right after treatment.
4
Remove gross soiling immediately.
4
Wipe-disinfect the medical device before transport.
4 Do not place in solutions or similar substances.
7.2 Manual Reprocessing
CAUTION
Never reprocess this medical device in an ultrasonic cleaner.
Malfunction and material damage.
4
Reprocess by hand only.
7.2.1 Manual external cleaning
4 Clean all outer surfaces of the DIAGNOdent display 2191 with a cloth
moistened with water and with one of the specified disinfectants if neces-
sary.
4
Comply with the instructions of the disinfectant manufacturer.
7.2.2 Manual internal cleaning
This product is not designed for manual internal cleaning.
7.2.3 Manual external disinfection
CAUTION
Never reprocess the device in an ultrasonic cleaner.
Malfunction and material damage.
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.