Low Endotoxin Cleanroom Wipes
Low Endotoxin Cleanroom Wipes Engineered Clean to Meet the Exacting Standards of the Pharmaceutical, Healthcare, and Medical Device Industries.
Endotoxins pose a substantial risk to regulated industries. If not properly addressed within your cleaning protocols and environmental monitoring, the outcomes can be disastrous. While many cleaning procedures focus on kill rate and eradicating harmful living microorganisms with antibacterial reagents such as phenolic, quaternary ammonium solutions, radiation, and other forms of sterilization; there is a hidden menace still lurking on the surface that you cannot see. Enter pyrogens, fever inducing endotoxins left behind from dead gram-negative bacteria. While disinfectants excel at rendering the bacteria as non-viable, the byproducts that they shed, can be deadly.
Regulated industries are faced with a difficult task: Kill the bacteria, but also remove the dead bacteria. Using wipes that are not tested and validated for low endotoxins levels can exacerbate the situation and can often contribute to endotoxin contamination.
Low Endotoxin Wipes to the Rescue
Our new line of Low Endotoxin wipes are lot-to-lot tested to ensure they meet or exceed the requirements set by USP & FDA standards based on the maximum allowable thresholds for endotoxins across key regulated industries. In addition, we recommend using WFI (water for injection) in conjunction with a low endotoxin wipe for effective removal of disinfectant solutions and endotoxins after surface disinfection has taken place to ensure you have neutralized the threat of endotoxins in your environment.
- Implantable devices
- Instruments & Tools
- Surgical Kits
- Pharmaceutical Manufacturing
- Medical Device
- Healthcare / Surgical Suite
- Other key EPA, FDA regulated industries