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KLS Martin group marSeal5 plus Gebrauchsanweisung Seite 82

Bipolares versiegelungssystem
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  • DEUTSCH, seite 9
Prior to each sterilization, the instruments must undergo a complete visual inspection and functional check
for damage and wear, see section 6.5.1 "Inspection and Functional Check", page 80.
Damaged instruments or their components must be immediately appraised by the manufacturer or an
authorized partner and repaired or replaced, respectively.
Repeat the cleaning if a visual check reveals tissue residues on the instrument, or if the blade is still in the
instrument, see section 6.4 "Cleaning and Disinfection", page 77.
The maximum number of allowed reprocessing cycles must not be exceeded, see also
section 6.1 "Limitations and Restrictions on Cleaning, Disinfection and Sterilization", page 72.
Risk of infection in case of non-sterile handling!
Improper sterilization and non-sterile application can lead to serious health hazards to patients.
The operator/user is responsible for cleaning, sterilizing and re-sterilizing the instrument. It is essential
that national regulations, including restrictions, be observed.
Sterilization must be carried out according to a validated steam sterilization process, for example in a
sterilizer complying with DIN EN 285:2009 and validated in accordance with DIN EN ISO 17665-1:2006.
• Approved sterilization packaging (e.g. acc. to DIN EN 868, ISO 11607) must be used for sterilization,
subsequent transportation and storage.
• Sterilization packaging must comply with the applicable standards and norms.
Danger of infection and risk of damage in case of improper processing!
Non-sterile handling can cause severe health risks for the patient.
• After each use, remove and dispose of the blade holder according to the applicable regulations!
• Never reprocess and/or reuse blade holders! Processing can damage the instrument! Processing the
blade holders can damage the instrument!
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Bipolar Sealing System marSeal5 plus/ - Maryland
One indicator must be broken out of the cycle counter after
each application and before re-sterilization. Use a ballpoint
pen or a similar object to remove it. By pressing the indicator
slightly, it is broken out.
Instructions for Use
Revision 06

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Marseal5 plus maryland

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