Packaging - KaVo INTRAsurg 300 Instructions For Use Manual

Surgical implant rotary system non optic unit
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Instructions for use INTRAsurg 300 / INTRAsurg 300 plus
6 Preparation methods DIN EN ISO 17664 | 6.3 Sterilisation in a steriliser in compliance with DIN EN 13060
CAUTION
Product damage
Contact corrosion
▶ Remove the sterilised item from the autoclave immediately after sterilising and
drying.
CAUTION
Crystallising saline solution
Malfunctions
▶ Rinse all hoses and drain them completely before they are sterilised.
Note
The user is responsible for observing the regulations and conditions for sterility.
After each patient, dispose of the coolant reservoir, rinse the hoses, and completely
drain and sterilise them.
Note
When treating patients who may have an acute, critical infectious disease, be sure
to observe the hygienic measures cited in applicable publications and reports. If
possible, use suitable disposable products to avoid the transmission of critical
pathogens. These protect the user, the patient and all participants in the surgery.
A microbiologically appropriate coolant liquid must be used. Only use prescribed
isotonic saline solution E NaCl 0.9 (identified as an infusion solution; follow the
instructions on the package insert) for cooling and spraying wounds. All materials
that are contaminated from the dental and medical fields must suitably processed
and sufficiently identified after cleaning and sterilisation (RKI recommendation,
www.rki.de).
See also: 6.1.3 Rinse the hoses, Page 47
The KaVo medical devices released for sterilisation have a maximum temperature
resistance of 138 ℃.

6.3.1 Packaging

The sterilisation bag must be large enough for the items to be sterilised so that the
bag is not stretched. The quality and use of the packaging of the items to be sterilised
must satisfy the applicable standards and be appropriate for sterilising.
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Intrasurg 300 plus

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