Contents1 Documentation 31.1 Associated documentation 31.2 Electronic documentation 32 Warnings 42.1 Federal Law 42.2 Warning applicable to all countries in which the device is sold 42.3 User population 42.4 Specific user training 42.5 Patient population 42.6 Patient population restriction 42.7 Parts of the body or types of tissues treated 52.8 Applied parts 52.9 Essential performance 52.10 Basic safety in normal use 52.11 Normal usage conditions 52.12 Service life 53 Required information 73.1 Indication for use 73.2 Operating principle 73.3 Connecting and disconnecting accessories during use 73.4 Repairing or modifying the medical device 73.5 Warranty 73.6 Latest document update 73.7 Date of first CE marking 74 Interactions, contraindications, prohibitions 94.1 Contraindications 94.2 Using accessories not supplied by the manufacturer 94.3 Prohibited uses 95 Unpacking the medical device 116 Installing the medical device 136.1 Fitting a nozzle 136.1.1 Supra 120° nozzle 136.1.2 Perio easy nozzle 136.1.3 Perio nozzle 136.1.4 Perio Maintenance nozzle 147 Dispensing a treatment 157.1 Accessory usage conditions 157.2 Pre-use test 157.3 First use 157.3.1 Turbine adapter 157.3.2 Powder tank 157.3.3 Filling the tank 157.3.4 Setting the irrigation flow 157.3.5 Using the medical device 157.4 Switching off the medical device 168 Disinfection and sterilising 178.1 Cleaning cycle limits 178.2 Clean and disinfect the medical device 178.3 Containment and transportation 178.4 Preparation for pre-disinfection 178.5 Pre-disinfection 17