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77.6   P

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.

Seal each medical device individually in a sterilised item package!

 

 

Setup methods according to DIN EN ISO 17664

51

77.7   S

Sterilisation

Sterilisation in a steam steriliser (autoclave) in accordance with EN 13060/

ISO 17665-1 (e.g. KaVo STERIclave B 2200 / 2200 P)

CAUTION

Premature wear and malfunctions from improper servicing and care.

Reduced product life.

▶ Before each sterilisation cycle, service the medical device with KaVo

care products.

 

 

Setup methods according to DIN EN ISO 17664

52

CAUTION

Contact corrosion due to moisture.

Damage to product.

▶ Immediately remove the product from the steam steriliser after the

sterilisation cycle!

The KaVo medical device has a maximum temperature resistance up to

138 ℃ (280.4 °F).

Setup methods according to DIN EN ISO 17664

53

(Depending on the available autoclave,) select a suitable procedure from

the following sterilisation processes:

▪ Autoclave with three times initial vacuum:

at least 3 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4

°F)

Drying time: 20 min.

▪ Autoclave using the gravitation method:

at least 10 minutes at 134 °C -1 °C / +4 °C (273 °F -1.6 °F / +7.4

°F) or alternatively

Drying time: 30 min.

at least 60 minutes at 121 °C -1 °C / +4 °C (250 °F -1.6 °F / +7.4

°F)

Drying time: 30 min.

Use according to the manufacturer's Instructions for Use.

 

 

Setup methods according to DIN EN ISO 17664

54

Summary of Contents for INTRAmatic contra-angle 80 ES

Page 1: ...ger levels 8 2 2 Safety instructions 9 3 Product description 15 3 1 Purpose Proper use 16 3 2 Technical data 18 3 3 Transportation and storage conditions 19 Contents 1 4 4 First use 21 4 1 Check the a...

Page 2: ...Sterilisation 52 7 8 Storage 55 8 8 Tools and consumables 56 9 Terms and conditions of warranty 58 Contents 4 1 1 U User instructions Dear User Congratulations on purchasing this KaVo quality product...

Page 3: ...NING WARNING indicates a hazardous situation that can cause death or serious injury Safety 8 DANGER DANGER indicates a hazardous situation that can directly cause death or serious injury 2 2 S Safety...

Page 4: ...s at KaVo branches throughout the world Technicians specially trained by KaVo The following guidelines must be observed to ensure save use of the elec trically driven handpieces The service instructio...

Page 5: ...l device may only be used for the described application by a knowledgeable user The following must be observed the applicable health and safety regulations the applicable accident prevention regulatio...

Page 6: ...RH to 95 RH Product description 19 Air pressure 700 hPa to 1060 hPa 10 psi to 15 psi Protect from moisture Product description 20 4 4 F First use WARNING Hazard from nonsterile products Infection dan...

Page 7: ...eration 24 5 5 1 A Attaching the medical device Place the medical device on the LUX motor coupling and lock it into place Before each treatment pull on the medical device to see if it is securely seat...

Page 8: ...r or grinder is securely attached by pulling on it Operation 28 5 5 4 R Removing the milling tool or diamond grinder CAUTION Hazard from rotating tools Laceration Do not carelessly contact rotating to...

Page 9: ...1 T Troubleshooting Exchanging the O rings on the motor coupling CAUTION Hazard from improper care of the O rings Malfunctions or complete failure of the product Do not use Vaseline or other grease o...

Page 10: ...fectors 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 medicle...

Page 11: ...ing 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 U...

Page 12: ...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 disinfecta...

Page 13: ...le tip in the opening and spray Carry out the servicing according to the instructions in the section Care with KaVo Spray Setup methods according to DIN EN ISO 17664 48 7 7 5 2 C Care products and sys...

Page 14: ...KaVo care products Setup methods according to DIN EN ISO 17664 52 CAUTION Contact corrosion due to moisture Damage to product Immediately remove the product from the steam steriliser after the steril...

Page 15: ...to this KaVo medical device KaVo provides the end customer with a warranty of proper function and guarantees zero defects in respect of material and processing for a period of 24 months from data of i...

Page 16: ...consequences are derived 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 pu...

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