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77.3.3   D

Disinfection: Machine disinfection - external and internal

KaVo recommends thermodisinfectors in accordance with EN ISO 15883

that are operated with alkaline cleaning agents at a pH of max. 10 (e.g.

Miele G 7781 / G 7881 – validation was performed with the ""VARIO-TD"

programme, "neodisher

®

 mediclean" cleaning agent, "neodisher

®

 Z" neu‐

tralisation agent, and "neodisher

®

 mielclear" rinsing agent and extends only

to the compatibility of materials with respect to KaVo products).

For program settings as well as cleansers and disinfectants to be used,

please refer to the Instructions for Use of the thermodisinfector (com‐

plying with max. pH value of 10).

In order to prevent negative effects on the medical device, make sure

that the interior and the exterior of the medical device are dry, and then

lubricate immediately with care agents from the KaVo care system.

 

 

 

Setup methods according to DIN EN ISO 17664

47

77.4   D

Drying

Manual drying

Blow off the outside and inside with compressed air until water drops

are no longer visible.

Machine drying

The drying procedure is normally part of the cleaning program of the ther‐

modisinfector.

Follow the instructions for use of the thermodisinfector.

 

 

 

 

 

 

Setup methods according to DIN EN ISO 17664

48

77.5   C

Care products and systems - Servicing

WARNING

Sharp cutters or grinders in the medical device.

Risk of injury from sharp or pointed cutters or grinders.

▶ Remove cutter or grinder.

CAUTION

Premature wear and malfunctions from improper servicing and care.

Reduced product life.

▶ Perform proper care regularly!

 

Setup methods according to DIN EN ISO 17664

49

Note
KaVo only guarantees that its products will function properly when the care

products used are those listed as accessories, as they were tested for

proper use on our products.

7.5.1   C

Care products and systems - Servicing: Care with KaVo Spray

KaVo recommends servicing the product after each time it is used, i.e. after

each automatic cleaning and before each sterilisation.

Remove cutter or grinder.

 

Cover the product with the CLEANpac bag.

Place the product on the cannula and press the spray button for one

second.

 

 

 

Setup methods according to DIN EN ISO 17664

50

Summary of Contents for INTRAcompact contra-angle 0768 LHC

Page 1: ...danger levels 8 2 2 Safety instructions 9 3 Product description 16 3 1 Purpose Proper use 17 3 2 Technical Data 19 3 3 Transportation and storage conditions 20 Contents 1 4 4 First use 22 4 1 Check th...

Page 2: ...e 52 Contents 3 7 6 Packaging 55 7 7 Sterilisation 56 7 8 Storage 58 8 8 Auxiliary equipment 60 9 Terms and conditions of warranty 61 Contents 4 1 1 U User instructions Dear User Congratulations on pu...

Page 3: ...death or serious injury Safety 8 DANGER DANGER indicates a hazardous situation that can directly cause death or serious injury 2 2 S Safety instructions WARNING Hazard to the care provider and patien...

Page 4: ...nging the speed and the direction of rotation The dental treatment unit connected must have control equipment for changing the speed and direction of rotation A note is to be included in the documents...

Page 5: ...ial cavities and crown preparations removal of fillings processing of tooth and restoration surfaces A medical device according to relevant national statutory regulations Product description 17 P Prop...

Page 6: ...s hazardous to start up the product after it has been stored refrigerated This can cause the product to malfunction Prior to start up very cold products must be heated to a temperature of 20 C to 25 C...

Page 7: ...ing to a minimum of 50 cm3 min First use 24 5 5 O Operation 5 1 A Attaching the medical device WARNING Release of the medical device during treatment A medical device that is not properly locked in pl...

Page 8: ...meter max 5 mm Operation 28 WARNING Use of unauthorised tools Injury to the patient or damage to the medical device Observe manufacturer instructions and use the tool properly Only use tools that do n...

Page 9: ...efully press the pushbutton with your thumb and simultaneously remove the tool Operation 32 DANGER Hazard from defective checking system The tool can fall out and cause injury Pull on the tool to chec...

Page 10: ...o the grooves Troubleshooting 36 6 6 2 2 T Troubleshooting Cleaning the spray nozzle CAUTION Hazard from insufficient amount of spray water Insufficient spray water can cause the medical device to ove...

Page 11: ...nfector com plying with max pH value of 10 In order to prevent negative effects on the medical device make sure that the interior and the exterior of the medical device are dry and then lubricate imme...

Page 12: ...sinfect in a thermodisinfector or manually Setup methods according to DIN EN ISO 17664 44 7 7 3 1 D Disinfection Manual disinfection external KaVo recommends the following products based on material c...

Page 13: ...ed air until water drops are no longer visible Machine drying The drying procedure is normally part of the cleaning program of the ther modisinfector Follow the instructions for use of the thermodisin...

Page 14: ...oduct See also Instructions for use K KaVo SPRAYrotor 7 5 3 C Care products and systems Servicing Servicing with KaVo QUATTROcare Cleaning and care unit with expansion pressure for effective cleaning...

Page 15: ...are products Setup methods according to DIN EN ISO 17664 56 CAUTION Contact corrosion due to moisture Damage to product Immediately remove the product from the steam steriliser after the sterilisation...

Page 16: ...r repair 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 mandat...

Page 17: ...1 004 8195 kb 20101015 03 en...

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