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COMPLIANCE INFO_1987-2019
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COMPLIANCE INFO_1987-2019
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Last modified
4/19/2023 4:04:55 PM
Creation date
8/25/2021 3:57:02 PM
Metadata
Fields
Template:
EHD - Public
ProgramCode
4500 - Medical Waste Program
File Section
COMPLIANCE INFO
FileName_PostFix
1987-2019
RECORD_ID
PR0450001
PE
4522
FACILITY_ID
FA0002864
FACILITY_NAME
DAMERON HOSPITAL
STREET_NUMBER
525
Direction
W
STREET_NAME
ACACIA
STREET_TYPE
ST
City
STOCKTON
Zip
95203
APN
13715304
CURRENT_STATUS
01
SITE_LOCATION
525 W ACACIA ST
P_LOCATION
01
P_DISTRICT
001
QC Status
Approved
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SJGOV\cfield
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EHD - Public
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Lr <br />INFORMATION BULLETIN <br />ATIO Disposable Biological -PLUS Test Pack INFORMATION BULLETIN <br />No. 41380 <br />with SteriGage® Integrator and Small Biological Catalog Number: <br />Indicator for Steam Sterilization 41380 <br />For use in 250°F (121 °C) gravity or 270°F (132°C) pre -vacuum steam <br />sterilizers. <br />• New, accurate, pre-packaged disposable test pack for use with every load in 250°F (121°C) gravity or 270°F <br />(132°C) pre -vacuum steam sterilizers. <br />• Immediately indicates whether a sterilization cycle was adequate, before the load has been released. <br />• Each pack contains a SteriGage® Steam Sterilization Integrator for immediate results, and a small Biological <br />Indicator with Bacillus stearothermophilus spores. <br />• Pre -packed for consistent, accurate results. <br />• Equivalent to biological test packs recommended by AAMI.* <br />• Helps reduce the risk of recalls. <br />• Enclosed in shelf packs to maintain proper humidity levels. <br />• Saine proven technology as all ATI test packs. <br />Routine monitoring of steam sterilization cycles with a test pack is an important and necessary quality control <br />function for the Central Supply Department. Test packs are utilized because they pose the greatest challenge to the <br />sterilization cycle. <br />ATI Disposable Biological -PLUS Test Packs for Steam Sterilizers are specifically made for testing every load in <br />gravity 250°F (121°C) and 270°F (132°C) pre -vacuum steam sterilizers. Each pack consists of a SteriGage Steam <br />Sterilization Integrator and a Biological Indicator (BI) specially positioned in a small package of porous substrate <br />with a moisture impervious, quality CSR wrap. The test pack is closed with a label which has a steam process <br />indicator on its border. After sterilization, the SteriGage Integrator can be read immediately. Results of this testing <br />can be recorded on the area provided on back of the SteriGage Integrator and on the record card inside the pack. The <br />BI is incubated at this time. <br />Although small in size, ATI test packs have been carefully constructed to provide extremely accurate results. <br />Rigorous clinical testing has shown that ATI test packs are equivalent to AAMI biological test packs. <br />Where and how they are used: <br />Use a Biological -PLUS Test pack in every load to determine if the parameters of sterilization have been met. It <br />should be placed horizontally in the bottom front of a fully loaded steam sterilizer. Run the sterilizer through a <br />normal cycle. Make sure the recording chart is in operation and properly marked (this becomes part of the test <br />record). <br />After the sterilizer cycle, open the test pack and read the SteriGage Integrator. The Integrator will clearly <br />indicate ACCEPT or REJECT. When an ACCEPT reading has been obtained, it is safe to assume that the pack <br />containing the Integrator has been exposed to adequate sterilization conditions. If the Integrator indicates REJECT, <br />the proper conditions for sterilization have not been met. Immediate action should be taken when results indicate that <br />sterility may not have been achieved. Record results on the back of the Integrator or on the record card and save as a <br />permanent record. <br />(over) <br />
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