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 ........................ 4 2 Safety..........................6 2.1 Infection hazard ......................6 2.2 Technical condition......................6 2.3 Accessories and combination with other equipment ............6 2.4 Qualification of personnel....................
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 1 User instructions Legal Manufacturer CE mark according to Medical Devices Directive EC 93/42 Please note the electronic instructions for use Note: Please note accompanying documents...
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 The instructions for use are a component of the product and must be read care- fully prior to use and be accessible at all times.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 2 Safety | 2.4 Qualification of personnel ▶ Only use accessories that have been approved for combination with the product by the manufacturer. ▶ Only use accessories that are equipped with standardised interfaces.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 2 Safety | 2.5 Service and repair ▶ KaVo recommends specifying in-house service intervals where the medical device is brought to a professional shop for cleaning, servicing and a func- tion check.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 3 Description of the device | 3.1 Purpose – Proper use 3 Description of the device SURGmatic S201 XL Pro SURGmatic S201 XL Pro Mat. no. 1.013.7541...
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 3 Description of the device | 3.3 Transportation and storage conditions Usable with surgical drill bits or burs with inner cooling or surgical tools with a hexagon head socket at the shaft.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 4 Start up and shut down | 4.1 Checking the amount of water 4 Start up and shut down WARNING Hazard from non-sterile products. Infection hazard for dentist and patient.
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Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 4 Start up and shut down | 4.1 Checking the amount of water ▶ Carefully plug the coolant hose in central position onto the media tube pro- ceeding in axial direction.
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 CAUTION The SURGmatic S201 L / XL Pro contra-angle handpiece consists of a shank and a head.
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 Detachment of the medical device during treatment.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 5 Operation | 5.6 Removing the milling tool or diamond grinder WARNING Use of unauthorised cutters or grinders. Injury to the patient or damage to the medical device.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 6 Troubleshooting | 6.1 Check for malfunctions 6 Troubleshooting 6.1 Check for malfunctions CAUTION Product heats up. Burn injury or product damage due to over-heating.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 7 Reprocessing steps in accordance with EN ISO 17664 | 7.1 Preparation at the site of use 7 Reprocessing steps in accordance with EN ISO 17664 7.1 Preparation 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 EN ISO 17664 | 7.3 Manual reprocessing 7.3 Manual reprocessing WARNING Sharp tool in the medical device. Injury hazard from sharp and/or pointed tool.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 7 Reprocessing steps in accordance with EN ISO 17664 | 7.4 Automated reprocessing WARNING Sharp tool in the medical device. Injury hazard from sharp and/or pointed tool.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 7 Reprocessing steps in accordance with EN ISO 17664 | 7.5 Care products and systems - Servicing 7.5 Care products and systems - Servicing CAUTION Improper service and care.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 7 Reprocessing steps in accordance with EN ISO 17664 | 7.5 Care products and systems - Servicing ▶ Remove the dental bur or diamond grinder.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 7 Reprocessing steps in accordance with EN ISO 17664 | 7.5 Care products and systems - Servicing ▶ Cover the medical device with the Cleanpac bag, and place it on the corres- ponding servicing adapter on the KaVo SPRAYrotor.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 7 Reprocessing steps in accordance with EN ISO 17664 | 7.6 Packaging 7.6 Packaging Note The sterile goods package must be large enough for the product so that the packaging is not stretched.
Instructions for use SURGmatic S201 XL Pro - 1.013.7541 SURGmatic S201 L Pro - 1.013.7540 8 Tools and consumables 8 Tools and consumables Available from dental suppliers. Material summary Mat.No. Spray head INTRA (KaVo Spray) 0.411.9911 Service coupling for heads 0.411.7941...
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 The following warranty conditions apply to this KaVo medical device: KaVo provides the end customer with a warranty of proper function and guar-...
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