B. Braun Aesculap Spine S4 Gebrauchsanweisung/Technische Beschreibung Seite 10

Aesculap Spine
4
S Spondylolisthesis Reduction Instrument (SRI)
Inspection, maintenance and checks
Damage
corrosion) to the product caused by
insufficient lubrication!
CAUTION Prior
lubricate moving parts (e.g.
joints, pusher components and
threaded
maintenance oil suitable for the
respective sterilization process
(e.g.
Aesculap STERILIT® I oil spray
JG600 or STERILIT® I drip
lubricator JG598).
Allow the product to cool down to room tempera-
ture.
After each complete cleaning, disinfecting, and
drying cycle, check that the instrument is: dry,
clean, operational, and free of damage (e.g. broken
insulation or corroded, loose, bent, broken, cracked,
worn or fractured components).
Dry the product if it is wet or damp.
Repeat cleaning and disinfection of products that
still show impurities or contamination.
Check that the product functions correctly.
Immediately put aside damaged or inoperative
products and send them to Aesculap Technical
Service, see Technical Service.
Check for compatibility with associated products.
8
(metal seizure/friction
to function checks ,
rods) with
for steam sterilization:
Packaging
Place the product in its holder or on a suitable tray.
Ensure that all cutting edges are protected.
Package trays appropriately for the sterilization
process (e.g. in Aesculap sterile containers).
Ensure that the packaging provides sufficient
protection against recontamination of the product
during storage (DIN EN ISO 11607).
Sterilization
Ensure that the sterilant can reach all external and
internal surfaces (e.g. by opening valves and
stopcocks).
Validated sterilization process:
– Disassemble the instrument.
– Steam sterilization through fractionated vacuum
process
– Steam sterilizer specified in DIN EN 285 and
validated in accordance with DIN EN ISO 17665
– Sterilization through
process at 134 °C/holding time 5 min
When sterilizing several instruments at the same
time in a steam sterilizer: ensure that the
maximum permitted load specified by the
manufacturer for the steam sterilizer is not
exceeded.
fractionated vacuum