Steris SYSTEM 1 endo User Manual

Quality Assurance Operator Manual T6800 Rev B
SYSTEM 1 endo Liquid Chemical Sterilant Processing System
8-1
QUALITY ASSURANCE
8
Documentation is a critical element in any Quality Assurance Program.
The printout that is provided for every cycle is a record containing the
key points recommended by the Association for the Advancement of
Medical Instrumentation (AAMI), the Association of Operating Room
Nurses (AORN), and the International Association of Healthcare Central
Service Material Management (IAHCSMM).
The printouts should be saved as part of your total Quality Assurance
Program. Depending on your state, regional, and your hospital and
departmental policies, you may wish to make a copy of the printout
for long term records. If a printout is missing for a load for any reason,
the load must be reprocessed using a fresh container of S40 Sterilant
Concentrate. If a printout is missing for a load due to a printer problem
or missing printer paper, refer to Section 9, Maintenance, or call
Customer Service.
Part 1:
Documentation
WARNING: If a printout
from the SYSTEM 1 endo
Processor is missing for
a load, the load must be
reprocessed.

Steris SYSTEM 1 endo Specifications

General

Brand	Steris
Model	SYSTEM 1 endo
Category	Laboratory Equipment
Language	English