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KaVo Multi-FINEair 333 M Instructions For Use Manual Download Page 39

6.7   Sterilisation

Sterilise in a steam steriliser (Autoclave) EN 13060/ISO 17665-1

CAUTION

Contact corrosion from moisture.

Damage to product

▶ Immediately remove the product from the steam steriliser after the

sterilisation cycle!

The medical device is temperature resistant up to 138℃ (280.4°F).

 

 

Preparation methods according to ISO 17664

37

Summary of Contents for Multi-FINEair 333 M

Page 1: ...Instructions for use Multi FINEair 333 M REF 1 001 8003...

Page 2: ...Distributed by KaVo Dental GmbH Bismarckring 39 D 88400 Biberach Tel 49 7351 56 0 Fax 49 7351 56 1488 Manufacturer Kaltenbach Voigt GmbH Bismarckring 39 D 88400 Biberach www kavo com...

Page 3: ...itions 6 2 Safety 8 2 1 Description of safety instructions 8 2 2 Purpose Proper use 10 2 3 Safety instructions 12 3 Product description 15 3 1 Technical Specifications 15 3 2 Transportation and storag...

Page 4: ...5 3 Inserting the cannula 23 5 4 Remove the cannula 24 5 5 Use 25 6 Preparation methods according to ISO 17664 27 6 1 Preparations at the site of use 27 6 2 Cleaning 28 6 2 1 Cleaning Manual cleaning...

Page 5: ...nual disinfection external 32 6 3 2 Disinfection Manual disinfection internal 33 6 3 3 Disinfection Machine disinfection external and internal 33 6 4 Drying 34 6 5 Care products and systems Servicing...

Page 6: ...ing this KaVo quality product Following the in structions below will allow you to work smoothly economically and safely Copyright by KaVo Dental GmbH Symbols Refer to chapter Safety Warning Important...

Page 7: ...unaut Europ enne A product with this mark meets the requirements of the applicable EC directive Action request Target group This document is intended for dentists and their assistants The section on s...

Page 8: ...ir Other claims of any nature whatsoever in particular with respect to compensation are excluded In the event of default gross negligence or intent this shall only apply in the absence of mandatory le...

Page 9: ...can be attributed to interventions on or changes made to the product by the customer or a third party not authorised by KaVo are excluded from the warranty Service warranty claims will only be accepte...

Page 10: ...uctions Warning symbol Structure DANGER The introduction describes the type and source of the danger This section portrays the possible consequences of non observance The optional step covers necessar...

Page 11: ...hree levels of danger will help avert property damage and injury CAUTION CAUTION indicates a hazardous situation that can cause damage to property or mild or moderate physical harm WARNING WARNING ind...

Page 12: ...oper use This medical device is Only intended for dental treatment Any other type of use or alteration to the product is impermissible and can be hazardous The medical device is intended for the follo...

Page 13: ...able health and safety regulations the applicable accident prevention regulations these instructions for use According to these regulations the user is required to Only use equipment that is operating...

Page 14: ...ek service support WARNING Hazard from contraindication If the soft tissue in the oral cavity is injured the compressed air may enable septic substances to enter the tissue Treatment must be discontin...

Page 15: ...s well as skin emphysema Keep the jet from directly contacting the gingiva and avoid the insuf flation of blown air into open wounds CAUTION Premature wear and malfunctioning from improper storage dur...

Page 16: ...the methods described in the KaVo instructions for use KaVo recommends specifying a service interval at the dental office for a licensed shop to clean service and check the functioning of the medical...

Page 17: ...uct description Multi FINEair 333 M Mat no 1 001 8003 3 1 Technical Specifications Drive pressure max 5 bar 73 psi Air consumption without the cannu la being screwed on max 20 NL min Product descripti...

Page 18: ...supplier 3 2 Transportation and storage conditions CAUTION It is hazardous to start up the medical device after it has been stored re frigerated This can cause the medical device to malfunction Prior...

Page 19: ...Temperature 20 C to 70 C 4 F to 158 F Relative humidity 5 to 95 non condensing Air pressure 700 hPa to 1060 hPa 10 psi to 15 psi Protect from moisture Product description 17...

Page 20: ...ts Infection danger to the care provider and patient Before first use and after each use sterilise the medical device 4 1 Attach the MULTIflex coupling Rub off the MULTIflex connection with a dry clot...

Page 21: ...Screw the MULTIflex LUX coupling to the turbine hose and tighten with the key Note Since light spray water and spray air are not required for the MultiFINE air deselect these functions First use 19...

Page 22: ...onnection to equipment Dirty and moist compressed air causes premature bearing wear Ensure dry clean and uncontaminated compressed air according to ISO 7494 2 To operate the Multi FINEair the drive pr...

Page 23: ...Multi FINEair and check the following pressures Induction air 5 bar 73 psi 4 3 Check O rings CAUTION Missing or damaged O rings Malfunctions and premature failure Make sure that all O rings are on the...

Page 24: ...is not properly locked can release from the MUL TIflex LUX during treatment Before each use check if the medical device is securely locked onto the MULTIflex LUX Precisely attach the medical device to...

Page 25: ...edical device Hold the coupling tight and pull the medical device off while twisting slightly 5 3 Inserting the cannula CAUTION Only use disposable cannulas with a lockable Luer connector ac cording t...

Page 26: ...Insert the cannula into the handpiece and turn it all the way to the right see arrow 5 4 Remove the cannula Turn the cannula to the left and remove Operation 24...

Page 27: ...nal Damage or injuries due to incorrect use of the Multi FINEair Make sure that the apex is closed Never use the Multi FINEair when the apex is open Make sure that the cannula is not wedged in the can...

Page 28: ...are difficult or impossible to see when wet Very fine isthmus and inlets to pulp canals accessory canal systems Fissure sealing for example with ampoule fissures prepared with air abrasive systems Tu...

Page 29: ...rd exists from contaminated medical devices Observe suitable personal protective measures Remove residual cement composite or blood at the site of use Dry the medical device to prepare it for transpor...

Page 30: ...trasonic unit Defects in the product Only clean in a thermodisinfector or manually 6 2 1 Cleaning Manual cleaning external Required accessories Tap water 30 C 5 C 86 F 10 F Brush such as a medium hard...

Page 31: ...rs in accordance with ISO 15883 1 e g Miele G 7781 G 7881 Validation was performed with the program VARIO TD the cleaner ne odisher mediclean the neutraliser neodisher Z and rinse neodisher mielclear...

Page 32: ...ction unit in accordance with ISO 15883 1 The interior of this product is not to be cleaned manually 6 2 4 Cleaning Automated internal cleaning KaVo recommends thermodisinfectors in accordance with IS...

Page 33: ...nd in the instructions for use of the thermodisinfector 6 3 Disinfection CAUTION Malfunctioning from using a disinfectant bath or chlorine containing dis infectant Defects in the product Only disinfec...

Page 34: ...ed on material compatibility The microbiological efficacy must be ensured by the disinfectant manufac turer Microcide AF by Sch lke Mayr liquid or cloths FD 322 by D rr CaviCide by Metrex Required too...

Page 35: ...ectant 6 3 2 Disinfection Manual disinfection internal To effectively set up the inside of the machine must be cleaned automat ically in a cleaning and disinfection unit in accordance with ISO 15883 1...

Page 36: ...lear and only refers to the material compatibility with KaVo products The program settings and cleansers and disinfectants that must be used can be found in the instructions for use of the thermodisin...

Page 37: ...the ther modisinfector 6 5 Care products and systems Servicing CAUTION Do not clean the Multi FINEair with oils or care spray Malfunction or damage to the product The Multi FINEair must not be lubric...

Page 38: ...tretched The quality and use of the sterilisation packaging must satisfy applicable standards and be suitable for the sterilisation procedure Individually weld the medical device in the sterilised ite...

Page 39: ...0 ISO 17665 1 CAUTION Contact corrosion from moisture Damage to product Immediately remove the product from the steam steriliser after the sterilisation cycle The medical device is temperature resista...

Page 40: ...following ster ilisation methods Autoclave with a triple pre vacuum for least four minutes at 134 C 1 C 273 F 1 8 F Autoclave using the gravitational method sterilise for at least 10 min at 134 C 1 C...

Page 41: ...8 Storage Prepared products must be stored protected germ free from dust in a dry dark and cool room Note Observe the expiration date of the sterilized item Preparation methods according to ISO 17664...

Page 42: ...7 Tools Obtainable from dental and medical suppliers Material summary Mat no STERIclave bags 0 411 9912 Tools 40...

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