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KaVo PROPHYflex 4 User Manual

KaVo PROPHYflex 4
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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.

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KaVo PROPHYflex 4 Specifications

General IconGeneral
BrandKaVo
ModelPROPHYflex 4
CategoryMedical Equipment
LanguageEnglish

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