KaVo SMARTmatic S20 K Instructions For Use Manual

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Instructions for use

SMARTmatic S20 – 1.011.6750

SMARTmatic S20 K – 1.011.6751

SMARTmatic S20 S – 1.011.6752

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Summary of Contents for KaVo SMARTmatic S20 K

Page 1 Instructions for use SMARTmatic S20 – 1.011.6750 SMARTmatic S20 K – 1.011.6751 SMARTmatic S20 S – 1.011.6752...
Page 2 Distributed by: Manufacturer: KaVo Dental GmbH KaVo Dental GmbH Bismarckring 39 Bismarckring 39 88400 Biberach 88400 Biberach Germany Germany Phone +49 7351 56-0 www.kavo.com Fax +49 7351 56-1488...
Page 3 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 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 ............
Page 4 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 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 SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 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 SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 1 User instructions WARNING In cases which – if not prevented – can lead to death or severe injury. CAUTION In cases which – if not prevented – can lead to minor or moderate injury.
Page 7 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 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.
Page 8 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 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.
Page 9 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 2 Safety | 2.6 Service and repair 4 Make sure that the user has read and comprehends the national and re- gional regulations.
Page 10 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 3 Product description | 3.1 Intended use 3 Product description SMARTmatic S20 (Mat. no. 1.011.6750) SMARTmatic S20 K (Mat. no. 1.011.6751) SMARTmatic S20 S (Mat. no. 1.011.6752) 3.1 Intended use...
Page 11 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 3 Product description | 3.2 Technical specifications (without light) ▪ the applicable health and safety regulations ▪ the applicable accident prevention regulations ▪ these Instructions for use According to these regulations, the user is required: ▪...
Page 12 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 3 Product description | 3.3 Transportation and storage conditions 3.3 Transportation and storage conditions CAUTION Startup after refrigerated storage. Malfunction. 4 Prior to startup, strongly refrigerated products must be allowed to warm up to a temperature of 20 °C to 25 °C (68 °F to 77 °F).
Page 13 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 4 Startup and shut down | 4.1 Checking the water quantity (S20 S only) 4 Startup and shut down WARNING Hazard from contaminated products.
Page 14 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 4 Startup and shut down | 4.1 Checking the water quantity (S20 S only) 14 / 32...
Page 15 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 5 Operation | 5.1 Attaching the medical device 5 Operation WARNING Rotating dental tool. Cuts, infection and burn injury. 4 Never push the press-button while the dental tool is rotating.
Page 16 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 5 Operation | 5.3 Inserting the dental bur 5.3 Inserting the dental bur NOTE Only use carbide burs or diamond grinders that conform to DIN EN ISO 1797 type 1, are made of steel or hard metal, and meet the following criteria: - Shaft diameter: 2.334 to 2.350 mm...
Page 17 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 5 Operation | 5.4 Removing the dental bur CAUTION Dental tool shaft slips inside the chucking system due to excessive speed of the dental tool or abrupt engagement of the dental tool.
Page 18 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 6 Checking for malfunctions and troubleshooting | 6.1 Checking for malfunctions 6 Checking for malfunctions and troubleshooting 6.1 Checking for malfunctions CAUTION Overheating of the device.
Page 19 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 6 Checking for malfunctions and troubleshooting | 6.2 Troubleshooting 4 Spray a lint-free cloth with KaVo Spray, apply it to the new O-rings and in- sert them in the recesses.
Page 20 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 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...
Page 21 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.2 Manual reprocessing 7.2 Manual reprocessing WARNING Incomplete disinfection. Patients, users or third parties could be infected by contaminated medical devices.
Page 22 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.2 Manual reprocessing 4 Allow the cleaning agent to act for 5 minutes.
Page 23 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.3 Automated reprocessing 7.3 Automated reprocessing WARNING Sharp dental tool in the medical device.
Page 24 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.4 Care products and systems - Servicing 7.3.2 Pre-cleaning Accessories required: ▪...
Page 25 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.4 Care products and systems - Servicing NOTE KaVo guarantees the proper function of KaVo products only if the care products listed by KaVo as accessories are used, since these were tested for proper use on our products.
Page 26 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.5 Packaging NOTE End the chuck service mode. Option 1: Place the dental handpieces in the QUATTROcare PLUS 2124 A, close the front flap and start the service procedure.
Page 27 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 7 Reprocessing steps in accordance with ISO 17664-1 / ISO 17664-2 | 7.7 Storage NOTE Comply with the expiry date of the sterilised items.
Page 28 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 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...
Page 29 Instructions for use SMARTmatic S20 – 1.011.6750, SMARTmatic S20 K – 1.011.6751, SMARTmatic S20 S – 1.011.6752 9 Terms and conditions of warranty 9 Terms and conditions of warranty This KaVo medical device is subject to the following warranty conditions:...

This manual is also suitable for:

Smartmatic s20 Smartmatic s20 s 1.011.6750 1.011.6751 1.011.6752