background image

Instructions for use elements™ 8:1

9 Terms and conditions of warranty

30 / 32

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-
antees zero defects in respect of material and workmanship for a period of 12
months from the date of the invoice, subject to the following conditions:
In case of justified complaints, KaVo will honour its warranty with a free re-
placement or repair. Other claims of any kind whatsoever, in particular with re-
spect to compensation, are excluded. In the event of default, gross negligence
or intent, this shall only apply in the absence of mandatory legal regulations to
the contrary.
KaVo shall not be liable for defects and their consequences that have arisen or
may arise from natural wear, improper handling, cleaning or maintenance, non-
compliance with operating, maintenance or connection instructions, calcination
or corrosion, contaminated air or water supplies or chemical or electrical factors
deemed abnormal or impermissible in accordance with KaVo's instructions for
use or other manufacturer's instructions. The warranty granted does not usually
extend to lamps, optical fibres made of glass and glass fibres, glassware, rub-
ber parts, and the colourfastness of plastic parts.
All liability is excluded if defects or their consequences originate from manipula-
tions or changes to the product made by the customer or a third party that is
not authorised by KaVo.
Warranty claims will only be accepted if the product is submitted along with
proof of purchase in the form of a copy of the invoice or note of delivery. The
dealer, purchase date, type, and serial number must be clearly evident from
this document.

Summary of Contents for 815-1655

Page 1: ...Instructions for use elements 8 1...

Page 2: ...al com Manufacturer KaVo Dental GmbH Bismarckring 39 88400 Biberach Germany www kavo com Distributed by Kerr Australia Pty Limited Unit 6 12 Mars Road Lane Cove West New South Wales 2066 Australia 61...

Page 3: ...6 1 Check for malfunctions 19 6 2 Troubleshooting 19 6 2 1 Replacing the O rings on the motor coupling 19 7 Reprocessing steps in accordance with ISO 17664 21 7 1 Preparations at the site of use 21 7...

Page 4: ...9 Terms and conditions of warranty 30 Instructions for use elements 8 1 Table of contents 4 32...

Page 5: ...00 KERR 123 Homepage www kerrdental com Email KerrCustCare kavokerr com Target group This document is for dentists and dental office staff The section on startup is also intended for the service staff...

Page 6: ...not dispose this product into the ordinary municipal waste or garbage system Properly dispose of non corrugated fiberboard Properly dispose of polyethylene Properly dispose of all other plastics such...

Page 7: ...structions for use elements 8 1 1 User instructions CAUTION In cases which if not prevented can lead to minor or moderate in jury NOTICE In cases which if not prevented can lead to material damage 7 3...

Page 8: ...u deviate from this procedure it is essential to make sure that the re processing is effective Reprocess the product and accessories appropriately before disposal If there is any injury to soft tissue...

Page 9: ...uthorised purposes 2 4 Accessories and combination with other equipment Use of un authorised accessories or un authorised modifications of the device could lead to injury Only use accessories that hav...

Page 10: ...vicing and a func tion check Define the service interval depending on the frequency of use As a result of the use of NON KaVo original spare parts during the repair parts such as covers may become und...

Page 11: ...Instructions for use elements 8 1 3 Product description 2 6 Service and repair 3 Product description elements 8 1 PN 815 1655 11 32...

Page 12: ...ly trained user You need to comply with the following the applicable health and safety regulations the applicable accident prevention regulations these Instructions for use According to these regulati...

Page 13: ...Consult instructions for use Please note the electronic instructions for use Certification CE mark Communaut Europ enne Medical device labelling of medical devices Product characteristics Manufacturer...

Page 14: ...TICE Startup after refrigerated storage Malfunction 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 Temperature 20 C to 70 C 4...

Page 15: ...zard Reprocess and sterilise the product and accessories before disposal See also 2 7 Reprocessing steps in accordance with ISO 17664 Page 21 NOTICE Damage from soiled and moist cooling air Contaminat...

Page 16: ...ile the drive motor is rotat ing NOTICE Pressing the foot switch while attaching or detaching the medical device Property damage to the medical device Do not connect or remove the medical device while...

Page 17: ...y Pull on the dental bur to check if the clamping system works properly and if the dental bur is firmly clamped Wear gloves or a thimble when you check insert or remove the bits to prevent injury and...

Page 18: ...tal bur Lacerations and damage to the chuck system Do not touch the rotating dental bur Never push the push button while the dental bur is rotating Remove the dental burs from the medical device after...

Page 19: ...ose and cause injury Aspiration swallowing of parts and danger of suffocation Only use spare parts that comply with the specification for repair original KaVo spare parts comply with the specification...

Page 20: ...Instructions for use elements 8 1 6 Checking for malfunctions and troubleshooting 6 2 Troubleshooting 20 32 Push the O ring to the front and remove it Insert new O rings into the grooves...

Page 21: ...always wear protect ive gloves Remove the tool from the medical device Remove all residual cement composite or blood immediately Do not place in solutions or similar substances 7 2 Manual Reprocessing...

Page 22: ...ot meet these requirements the process must be concluded by disinfection of the unit s without packaging using a steam steriliser NOTICE Never disinfect the medical device with chloride containing pro...

Page 23: ...roducts use only disinfection agents that have been released by KaVo with respect to the compatibility of materials e g WL cid made by ALPRO Cover the medical device with the KaVo CLEANpac bag and pla...

Page 24: ...lly or in a washer disinfector only 7 3 1 Automated internal and external cleaning and internal and external disinfection KaVo recommends washer disinfectors according to EN ISO 15883 1 which are oper...

Page 25: ...each use i e after each cleaning disinfection and before each sterilisation Remove the tool from the medical device Cover the medical device with the KaVo CLEANpac bag and place it on the correspondin...

Page 26: ...the far right A MULTIflex adaptor must be mounted there Press the handpiece together with the guide bush of the chuck to be ser viced against the tip of the service coupling Press the button marked wi...

Page 27: ...tion and before each sterilisation Remove the tool from the medical device Service the product in the QUATTROcare See also 2 Instructions for use KaVo QUATTROcare 2104 2104A 2124A Servicing the chuck...

Page 28: ...parameters Select a suitable process from the following sterilisation processes depending on the available steriliser Steriliser with triple pre vacuum at least 3 minutes at 134 C 1 C 4 C 273 F 1 6 F...

Page 29: ...10 units 0 411 9691 Cellulose pad 100 units 0 411 9862 Spray head INTRA KaVo Spray 0 411 9911 Service coupling INTRA QUATTROcare 1 009 6143 Material summary Mat no Adaptor INTRAmatic CLEANspray and D...

Page 30: ...consequences that have arisen or may arise from natural wear improper handling cleaning or maintenance non compliance with operating maintenance or connection instructions calcination or corrosion co...

Page 31: ......

Page 32: ...1 013 9552 bd 20210302 02 en...

Reviews: