|
3M
Attest Steam Packs -
The San-I-Pak
sterilization process can be monitored with a biological
indicator. We recommend the use of the 3M 1276 Attest Steam Pack.
This pack contains a biological indicator sample, indicator strips
and a record-keeping card. The  indicator
strips on the label and within the pack will change color to show
the pack was indeed steam processed. The biological indicator
located within the pack will show the ability of the San-I-Pak
to penetrate the barriers within the test pack, thus achieving
sterilization.
This pack
is a simple and effective method of challenging the sterilization
abilities of any autoclave system. With the San-I-Pak
unit the testing can be accomplished quickly and easily.
During a normal waste processing cycle the 3M Test Pack should
be placed in the chamber with the waste to be processed. By loading
the test kit last, near the door of the unit, it may be easily
retrieved upon completion of the processing cycle. The 3M 1276
Attest Steam Pack is designed to be the equivalent to the standard
linen pack (12" x 12" x 20", 12lbs.) which is recommended
by the Association of the Advancement of Medical Instrumentation
(AAMI). Note: This pack has been designed by 3M to duplicate
the Bowie Dick Towel Pack Testing of autoclaves. The test simulates
a load of waste, therefore does not require insertion into the
actual waste.
 After
removal from the San-I-Pak
the biological indicators contained within the 3M Test
Pack should be incubated at approximately 56°C. for 48 hours.
After incubation, the ample visually indicates growth or no growth
of the indicator spore. No color change (any growth) equals complete
sterilization.
The requirements
regarding the frequency of efficacy testing vary from state to
state. Please check with local authorities for the requirements
of your specific state.
Hospitals
Infection Control personnel may have a preferred method for testing
effectiveness if they are presently sterilizing infectious waste.
If not, San-I-Pak
can assist the facility with any method desired. Most
San-I-Pak
users employ either the 3M Attest Steam pack or the Therma-log
S Steam Sterilization Integrator for testing terminal destruction.
Many similar biological indicators containing Bacillus Stearothermophilus
are available. San-I-Pak
has been tested with the most stringent, recognized methods
throughout the United States. Results have been proven the San-I-Pak
to be one of the most effective, reliable system of steam
sterilization available for processing biohazardous waste.
Note: Strict
programming of the control electronics of all San-I-Pak
units prevent the discharge of un-sterilized waste. San-I-Pak
employs parametric motoring, which is superior to Biological
Test. The computer has a built-in steam table that enables constant
comparison of vessel temperature with vessel pressure. Other fail
safes such as time to vacuum, vacuum level, time to temperature,
droop control and vent time exceed conventional testing. In the
unusual occurrence of any discrepancy in the programmed parameters,
the process will be halted and then after correction cycle must
be restarted.
|
