Reprocessing Steps In Accordance With Iso 17664; Preparation At The Site Of Use; Disassembly; Manual Reprocessing - KaVo PROPHYflex 4 Instructions For Use Manual

Instructions for use PROPHYflex 4
7 Reprocessing steps in accordance with ISO 17664 | 7.1 Preparation at the site of use

7 Reprocessing steps in accordance with ISO 17664

7.1 Preparation at the site of use

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

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

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:
o
▪ Tap water 30 C ± 2
▪ Brush, e.g. medium-hard toothbrush
▶ Brush off under flowing tap water.
WARNING
WARNING
NOTICE
o o o
C (86 F ± 4 F)
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