B.Braun Aesculap BA720R Instrucciones De Manejo/Descripción Técnica página 7

►
Turn cutting cylinder 2 while pulling it out of bearings 20, see Fig. 4.
This completes the dismounting of cutting cylinder 2.
20
Fig. 4
Mounting the cutting cylinder
Note
To prevent transport damage, cutting cylinder 2 is protected by a piece of
cardboard on delivery. Remove the cardboard protection only after cutting
cylinder 2 has been mounted completely.
►
Insert the cutting cylinder 2 into the two bearings 20, see Fig. 4.
►
Hold cutting cylinder 2 at shaft 10 and press it into bearings 20 until
it clicks into position, see Fig. 3.
►
Turn shaft 10 and check cutting cylinder 2 for correct seating.
►
Close upper part 17 on lower part 14, see Fig. 2.
►
Turn cutting device 4 upside down so that the four screws 11 are vis-
ible, see Fig. 1.
►
Tighten screws 11 by hand.
►
Return cutting device 4 to its upright position.
►
Remove the piece of cardboard from cutting cylinder 2.
This completes the mounting of cutting cylinder 2.
6. Validated reprocessing procedure
The reprocessing instructions for the skin mesh der-
matome may differ from these instructions for use!
WARNING These instructions for use describe only the opera-
tion and reprocessing of the skin mesh dermatome
as of series number 4000.
►
For upgrades, please contact your national
B. Braun/Aesculap agency.
6.1 General safety instructions
Note
Adhere to national statutory regulations, national and international stan-
dards and directives, and local, clinical hygiene instructions for sterile pro-
cessing.
Note
For patients with Creutzfeldt-Jakob disease (CJD), suspected CJD or possi-
ble variants of CJD, observe the relevant national regulations concerning
the reprocessing of products.
2
20
Note
Mechanical reprocessing should be favored over manual cleaning as it gives
better and more reliable results.
Note
Successful processing of this medical device can only be ensured if the pro-
cessing method is first validated. The operator/sterile processing technician
is responsible for this.
The recommended chemistry was used for validation.
Note
If there is no final sterilization, then a virucidal disinfectant must be used.
Note
For up-to-date information about reprocessing and material compatibility,
see also the Aesculap Extranet at https://extranet.bbraun.com
The validated steam sterilization procedure was carried out in the Aesculap
sterile container system.
6.2 Single-use products
Infection hazard for patients and/or users and
impairment of product functionality due to reuse.
Risk of injury, illness or death due to contamination
WARNING
and/or impaired functionality of the product!
►
Do not reprocess the product!
Designation
Carrier plate
6.3 General information
Dried or affixed surgical residues can make cleaning more difficult or inef-
fective and lead to corrosion. Therefore the time interval between applica-
tion and processing should not exceed 6 h; also, neither fixating pre-
cleaning temperatures >45 °C nor fixating disinfecting agents (active
ingredient: aldehydes/alcohols) should be used.
Excessive measures of neutralizing agents or basic cleaners may result in
a chemical attack and/or to fading and the laser marking becoming
unreadable visually or by machine for stainless steel.
Residues containing chlorine or chlorides e.g. in surgical residues, medi-
cines, saline solutions and in the service water used for cleaning, disinfec-
tion and sterilization will cause corrosion damage (pitting, stress corro-
sion) and result in the destruction of stainless steel products. These must
be removed by rinsing thoroughly with demineralized water and then dry-
ing.
Additional drying, if necessary.
Only process chemicals that have been tested and approved (e.g. VAH or
FDA approval or CE mark) and which are compatible with the product's
materials according to the chemical manufacturers' recommendations
may be used for processing the product. All the chemical manufacturer's
application specifications must be strictly observed. Failure to do so can
result in the following problems:
■
Optical changes of materials, e.g. fading or discoloration of titanium or
aluminum. For aluminum, the application/process solution only needs
to be of pH >8 to cause visible surface changes.
■
Material damage such as corrosion, cracks, fracturing, premature aging
or swelling.
en
Article no.
BA721
BA722
BA723
5