Endotoxin Challenge Vials™
Endotoxin Challenge Vials™
Product Overview
UPDATE (May 2020):
We are discontinuing the performance of a sterility test for our Endotoxin Challenge VialsTM. As part of the production process, the stoppers are autoclaved prior to use. Additionally, all glassware is depyrogenated at extremely high temperatures well in excess of standard depyrogenation process conditions. These conditions provide for ample assurance that the vials and stoppers are suitable for production of Endotoxin Challenge VialsTM. Post filling, the product is lyophilized. Since there is no remaining water, conditions would not support growth of any organism to degrade the product. Therefore, there is no added value or additional quality assurance in performing a sterility test after production.
For use in oven validation studies, contains > 1,000 EU/vial. The vials may be tested using any of our endotoxin detection kits
Request More InfoBenefits
Does not contain filler
Applications
For oven validation studies
Storage and Content
> 1000 EU/VialSDS, CoA, and Instructions
Safety Data Sheets (SDS)
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Certificate of Analysis (CoA)
Please enter Lot Number, including all zeros, located on the product label and please take into account that it is case sensitive.