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KaVo INTRA shank C 09, Instructions For Use Manual

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KaVo INTRA shank C 09 Instructions For Use Manual Download Page 44

6.8   Packaging

Note
The sterilisation bag must be large enough for the instrument so that the

bag is not stretched.

The quality and use of the sterilised product packaging must satisfy ap‐

plicable standards and be suitable for the sterilisation procedure.

▶

Individually weld the medical device in the sterilised item packaging

(such as KaVo STERIclave bags Mat. no. 0.411.9912)!

 

 

Preparation methods according to ISO 17664

42

Summary of Contents for INTRA shank C 09

Page 1: ...Instructions for use INTRA shank C 09 REF 1 001 2278...

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: ...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 Specification 16 3 2 Transportation and storage condi...

Page 4: ...hods according to ISO 17664 26 6 1 Preparations at the site of use 26 6 2 Disassemble medical device 27 6 3 Assembling the medical device 28 6 4 Cleaning 28 6 4 1 Cleaning Manual cleaning external 28...

Page 5: ...and internal 36 6 6 Drying 37 6 7 Care products and systems Servicing 38 6 7 1 Care products and systems Servicing Care with KaVo spray 39 6 7 2 Care products and systems Servicing Care with the KaVo...

Page 6: ...this KaVo quality product By following the instructions below you will be able to work smoothly economically and safely Copyright by KaVo Dental GmbH Symbols Refer to Safety Warning chapter Important...

Page 7: ...eets the requirements of the applicable EC directive Sterilisable in steam up to 135 C 275 F Thermodisinfectable Target group This document is intended for dentists and their assistants The section on...

Page 8: ...air 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 l...

Page 9: ...ived from manipulations or changes to the product by the customer or a third party Service warranty claims will only be accepted if the product is submitted along with proof of purchase in the form of...

Page 10: ...tions Warning symbol Structure DANGER The introduction describes the type and source of the danger This section illustrates the potential consequences of non observance The optional step covers necess...

Page 11: ...he three 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...

Page 12: ...nt only All other types of use or alterations to the product are not permitted and can be hazardous The medical product is designed to be used with the corresponding heads in the following application...

Page 13: ...le 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 c...

Page 14: ...3 Safety instructions WARNING Hazard to the care provider and patient Damage irregular noise during operation excessive vibration unusual build up of heat Stop work and seek service support Safety 12...

Page 15: ...before long periods of nonuse The following individuals are authorized to repair and service KaVo prod ucts Technicians at KaVo branches throughout the world Technicians specially trained by KaVo To e...

Page 16: ...to clean service and check the functioning of the medical device This service in terval should take into account the frequency of use Service may only be provided by repair shops that have undergone t...

Page 17: ...3 Product description INTRA shank C 09 Mat no 1 001 2278 Product description 15...

Page 18: ...1 Maximum speed max 4 400 rpm The INTRA shank C 09 can be disassembled See also 6 2 Disassemble medical device Page 27 INTRA Heads can be inserted The reducing shank can be mounted on all INTRAmatic m...

Page 19: ...vice after it has been stored strongly refrigerated This can cause the medical device to malfunction Prior to start up very cold products must be heated to a temperature of 20 C to 25 C 68 F to 77 F T...

Page 20: ...Air pressure 700 hPa to 1060 hPa 10 psi to 15 psi Protect from moisture Product description 18...

Page 21: ...after each use sterilise the medical device 4 1 Cooling medium supply CAUTION Hazard of air embolism and skin emphysema There is a danger that the insufflation of spray in open wounds in the surgical...

Page 22: ...Cooling the drill bit or bur via external supply During surgical interventions comply with the necessary precautions regarding cooling Use physiological sterile cooling fluid Ensure that the supply o...

Page 23: ...device during treatment A medical device that is not properly locked in place can become discon nected from the motor coupling and fall off Carefully pull on the medical device before each treatment...

Page 24: ...CAUTION Removing and attaching the handpiece while the drive motor is rotating Damage to the catch Never attach or remove the reducing shank while the device is ro tating Operation 22...

Page 25: ...edical device to the LUX motor coupling until it locks into place and twist it until the catch audibly locks in place Pull on it to make sure that the medical device is securely affixed to the couplin...

Page 26: ...along its axis 5 3 Insert INTRA head CAUTION Loosening of the medical device during treatment If the head is not properly locked in place it can fall out during treatment Do not mount or remove the h...

Page 27: ...top Make sure that the catches engage prop erly Rotate the clamping ring against the direction of the arrow to close it and then tighten it 5 4 Removing the INTRA head Hold the clamping ring tight tur...

Page 28: ...medical devices Observe suitable personal protective measures Note Immediately disassemble and thoroughly clean the medical device after each surgical intervention since malfunctions could otherwise...

Page 29: ...er treatment Note For rehabilitation remove the head from the shank 6 2 Disassemble medical device Remove the INTRA head from the medical device Screw the conical sleeve on in counterclockwise directi...

Page 30: ...leaning CAUTION Malfunctions from cleaning in an ultrasonic unit Defects in the product Only clean manually or in a thermodisinfector 6 4 1 Cleaning Manual cleaning external Accessories required Tap w...

Page 31: ...tap water Note Never use alkaline or chlorine containing disinfectants 6 4 2 Cleaning Automated external cleaning KaVo recommends thermodisinfectors in accordance with ISO 15883 1 Preparation methods...

Page 32: ...ty with KaVo prod ucts The program settings and cleansers and disinfectants that must be used can be found in the instructions for use of the thermodisinfector Directly after automated cleaning treat...

Page 33: ...with KaVo DRYspray See also KaVo CLEANspray KaVo DRYspray Instructions for Use Note KaVo CLEANspray and KaVo DRYspray for manual interior cleaning are only available in the following countries Germany...

Page 34: ...the neutraliser neodisher Z and rinse neodish er mielclear and only refers to the material compatibility with KaVo prod ucts The program settings and cleansers and disinfectants that must be used can...

Page 35: ...ion CAUTION Malfunctioning from using a disinfectant bath or disinfectant containing chlorine Defects in the product Only disinfect in a thermodisinfector or manually Preparation methods according to...

Page 36: ...he following products based on material compatibility The microbiological efficacy must be ensured by the disinfectant manufac turer Microcide AF from Sch lke Mayr liquid or cloths FD 322 from D rr Ca...

Page 37: ...m the disinfectant manufacturer Note Observe the instructions for use for the disinfectant 6 5 2 Disinfection Manual disinfection internal For the effective re preparation the inside of the device mus...

Page 38: ...ediclean the neutraliser neodisher Z and rinse neodish er mielclear and only refers to the material compatibility with KaVo prod ucts The program settings and cleansers and disinfectants that must be...

Page 39: ...ssed air until water drops are no longer visible Machine drying The drying procedure is normally part of the cleaning program of the ther modisinfector Note Please observe the instructions for use of...

Page 40: ...product life Perform proper care regularly Note For care remove the head from the reducing shank Note KaVo only guarantees that its products will function properly when the care products used are thos...

Page 41: ...nds servicing the project after each time it used i e after each automatic cleaning and before each sterilisation Cover the product with the Cleanpac bag Place the product on the cannula and press the...

Page 42: ...ject after each time it used i e after each automatic cleaning and before each sterilisation Place the product on the appropriate coupling of the KaVo SPRAYrotor and cover it with a CLEANpac bag Servi...

Page 43: ...th expansion pressure for effective cleaning and care KaVo recommends servicing the project after each time it used i e after each automatic cleaning and before each sterilisation Servicing the produc...

Page 44: ...tched The quality and use of the sterilised product packaging must satisfy ap plicable standards and be suitable for the sterilisation procedure Individually weld the medical device in the sterilised...

Page 45: ...Autoclave EN 13060 ISO 17665 1 CAUTION Premature wear and malfunctions from improper servicing and care Reduced product life Before each sterilisation cycle service the medical device with KaVo care p...

Page 46: ...remove the product from the steam steriliser after the sterilisation cycle The medical device is resistant to temperatures up to 138 280 4 F KaVo recommends e g STERIclave B 2200 2200P from KaVo Cito...

Page 47: ...utoclave with gravitation process for least ten minutes at 134 C 1 C 273 F 1 8 F Autoclave with gravitation process for at least 60 minutes at 121 C 1 C 250 F 1 8 F Follow the manufacturer s instructi...

Page 48: ...Note Observe the expiration date of the sterilised item Preparation methods according to ISO 17664 46...

Page 49: ...ary Mat no Instrument stand 2151 0 411 9501 Cleanpac 10 units 0 411 9691 Cellulose pad 100 units 0 411 9862 Spray hose sterilisable yard ware 0 065 5188 Material summary Mat no KaVo CLEANspray 1 007 0...

Page 50: ...Material summary Mat no ROTAspray 2142 A 0 411 7520 QUATTROcare plus Spray 2108 P 1 005 4525 Tools 48...

Page 51: ......

Page 52: ...1 001 7360 kb 20100414 02 en...

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