Sutter Bison 730100-33 Manuel D'instructions page 11

Program steps
Process
Sterilization temperature
Sterilization time (holding time at
sterilization temperature)
Drying time
a Do not sterilize in hot air!
a Do not sterilize in STERRAD
a In case of potential contact with prions (CJD – risk of contamination), destroy the inst-
rument and do not use it again.
Storage / Transportation:
Store in a dry place. Protect from sunlight. Store and transport in secure containers /
packaging.
For returns, products must be cleaned, disinfected, and packed in sterile packaging.
Please note:
The instructions listed above have been validated by the manufacturer as suitable for
preparing a medical device for reuse. It is the responsibility of the reconditioner to ensure
that actual reconditioning with the equipment, materials, and personnel used in the recon-
ditioning facility achieves the desired result.
Serious incidents that occur in relation to the product must be reported to the manufacturer
and the responsible public authority in the member state in which the user and/or patient
resides.
The product may only be repaired by the manufacturer or an agent expressly authorized by
the manufacturer. Otherwise the warranty and any possible additional liability claims against
the manufacturer are voided.
Any change to the product or deviation from these instructions for use waives the liability
of Sutter Medizintechnik GmbH.
Changes reserved. Current version available at www.sutter-med.de.
®
STERRAD is a trademark of Johnson & Johnson, Inc.
FIG A: components
FIG B: assembly and functional test
FIG C: disassembly
FIG D: hazard notice
Parameters
Fractionated vacuum (3x)
132 °C (max. 138 °C plus tolerance
according to EN ISO 17665)
Min. 3 minutes
Not specified
®
!
English
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