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AAMI 11140-4
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AAMI 11140-4 2007 Edition, January 1, 2007 Sterilization of health care products — Chemical indicators — Part 4: Class 2 indicators as an alternative to Bowie and Dick test for detection of steam penetration
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Description / Abstract:
This part of ISO 11140 specifies the performance for a Class 2
indicator to be used as an alternative to the Bowie and Dick-type
test for steam sterilizers for wrapped health care goods
(instruments, etc., and porous loads).
NOTE The Bowie and Dick-type test is used for routine testing of steam sterilizers and validation of steam sterilization processes.
An indicator complying with this part of ISO 11140 incorporates a specified material which is used as a test load. This test load may, or may not, be re-usable. This part of ISO 11140 does not specify requirements for the test load, but specifies the performance of the indicator in combination with the test load with which it is intended to be used. The indicator specified in this part of ISO 11140 is intended to identify poor steam penetration but does not necessarily indicate the cause of this poor steam penetration.
This part of ISO 11140 does not include test methods to establish the suitability of these indicator systems for use in sterilizers in which the air removal stage does not include evacuation below atmospheric pressure.
NOTE The Bowie and Dick-type test is used for routine testing of steam sterilizers and validation of steam sterilization processes.
An indicator complying with this part of ISO 11140 incorporates a specified material which is used as a test load. This test load may, or may not, be re-usable. This part of ISO 11140 does not specify requirements for the test load, but specifies the performance of the indicator in combination with the test load with which it is intended to be used. The indicator specified in this part of ISO 11140 is intended to identify poor steam penetration but does not necessarily indicate the cause of this poor steam penetration.
This part of ISO 11140 does not include test methods to establish the suitability of these indicator systems for use in sterilizers in which the air removal stage does not include evacuation below atmospheric pressure.