KaVo PROPHYflex 4, Instructions For Use Manual

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Instructions for use PROPHYflex 4
7 Reprocessing steps in accordance with ISO 17664 | 7.1 Preparation at the site of use
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7 Reprocessing steps in accordance with ISO 17664
7.1 Preparation at the site of use
WARNING
Hazard from contaminated products.
Contaminated products are associated with an infection hazard.
▶ Take suitable personal protective measures.
▶ Reprocess the medical device as soon as possible after treatment.
▶ The medical device must be dry when transported to reprocessing.
▶ To minimise the risk of infection during reprocessing, always wear protect-
ive gloves.
▶
Remove all residual cement, composite or blood immediately.
▶
Do not place in solutions or similar substance.
7.2 Disassembly
WARNING
Incomplete reprocessing.
Infection hazard.
▶
To ensure complete reprocessing of all parts, the medical device needs to
be disassembled before reprocessing.
▶
Unscrew the powder container.
▶
Pull the gripping sleeve off.
▶
Remove the cannula from the gripping sleeve.
7.3 Manual Reprocessing
NOTICE
Never reprocess this medical device in an ultrasonic device.
Malfunction and material damage.
▶
Clean manually or in a washer disinfector only.
7.3.1 Manual external cleaning
Accessories required:
▪ Tap water 30
o
C ± 2
o
C (86
o
F ± 4
o
F)
▪ Brush, e.g. medium-hard toothbrush
▶ Brush off under flowing tap water.