Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 Table of contents Table of contents 1 User instructions ....................... 2 Safety..........................2.1 Infection hazard ......................7 2.2 Improper use ........................ 7 2.3 Technical condition ......................8 2.4 Accessories and combination with other equipment............
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 1 User instructions 1 User instructions Dear user, Congratulations on purchasing this KaVo quality product. By following the notes below you will be able to work smoothly, economically and safely.
Page 5
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 1 User instructions Serial number UDI symbol Manufacturer Note: Please note accompanying documents Follow the electronic instructions for use HIBC Code CE mark for medical devices...
Page 6
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 1 User instructions CAUTION In cases which – if not prevented – can lead to minor or moderate injury. CAUTION In cases which – if not prevented – can lead to material damage.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 2 Safety | 2.1 Infection hazard 2 Safety NOTE All serious events occurring in relation to the product must be reported to the manufacturer and the competent authority of the member state, in which the user and/or patient resides.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 2 Safety | 2.3 Technical condition 2.3 Technical condition A damaged product or damaged or NOT KaVo original components could injure patients, users or third parties.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 2 Safety | 2.6 Service and repair 4 Make sure that the user has read and fully comprehends the instructions for use. 4 Make sure that the user has read and comprehends the national and re- gional regulations.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 3 Description of the product | 3.1 Intended use 3 Description of the product SURGmatic S201 XL Pro (Mat. no. 1.013.7541) SURGmatic S201 L Pro (Mat. no. 1.013.7540) 3.1 Intended use...
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 3 Description of the product | 3.2 Technical Specifications 3.2 Technical Specifications CAUTION The contra-angle handpiece SURGmatic S201 L / XL Pro consists of a shank and a head.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 4 Startup and shut down | 4.1 Checking the amount of water 4 Startup and shut down WARNING Hazard from contaminated products. Patients, users or third parties could be infected by contaminated medical devices.
Page 13
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 4 Startup and shut down | 4.1 Checking the amount of water 4 Ensure that the coolant supply is free of air. 4 Cool the dental bur via the external and/or internal feed, if available. The supply can take place individually or via a coupling piece.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 5 Operation | 5.1 Inserting the head 5 Operation 5.1 Inserting the head WARNING Detaching the medical device during treatment. If the head is not properly locked in place, it can become detached during treat- ment.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 5 Operation | 5.3 Attaching the contra-angle handpiece to motor coupling 5.3 Attaching the contra-angle handpiece to motor coupling WARNING Detaching the medical device during treatment.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 5 Operation | 5.5 Inserting the dental bur 5.5 Inserting the dental bur NOTE Only use carbide burs or diamond grinders that conform to DIN EN ISO 1797...
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 5 Operation | 5.6 Removing the dental bur CAUTION Incorrectly clamped dental bur. Material damage to the chuck system, dental bur is difficult or impossible to re- move from the chuck system.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 6 Checking for malfunctions and troubleshooting | 6.1 Check for malfunctions 6 Checking for malfunctions and troubleshooting 6.1 Check for malfunctions CAUTION Overheating of the device.
Page 19
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 6 Checking for malfunctions and troubleshooting | 6.2 Troubleshooting 4 Use the nozzle needle (Mat. no. 0.410.0931) to clean the water passage on the spray nozzles.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.1 Preparations at the site of use 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 7.1 Preparations at the site of use...
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.3 Automated reprocessing 7.3 Automated reprocessing WARNING Sharp dental bur in the medical device.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.4 Care products and systems - Servicing 7.3.2 Automated internal and external cleaning and...
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.4 Care products and systems - Servicing KaVo recommends servicing the product as part of the reprocessing after each use, i.e.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.5 Packaging 7.5 Packaging NOTE The sterile goods package must be large enough to accommodate the product without stretching the packaging.
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 8 Optional aids and consumables 8 Optional aids and consumables Available from specialised dental dealers. Material summary Mat. no. INTRA Instrument stand 3.005.5204 Cleanpac 10 units 0.411.9691...
Instructions for use SURGmatic S201 XL Pro – 1.013.7541, SURGmatic S201 L Pro – 1.013.7540 9 Terms and conditions of warranty 9 Terms and conditions of warranty This KaVo medical device is subject to the following warranty conditions: KaVo grants the end customer a warranty of proper function and guarantees...
Need help?
Do you have a question about the SURGmatic S201 XL Pro and is the answer not in the manual?
Questions and answers