CONTAINS SHOULD BE CONSIDER FOR FOOD, SPECIES,COSMETICS AND MEDICAL DEVICES
Sterilization is a term referring to any process that eliminates (removes) or kills all forms of microbial life, including transmissible agents (such as fungi, bacteria, viruses, spore forms, etc.) present on a surface, contained in a fluid, in medication, or in a compound such as biological culture media. Sterilization can be achieved by applying the proper combinations of heat, chemicals, irradiation, high reassure, and filtration
The term has evolved to include the disabling or destruction of infectious proteins such as prions related to Transmissible Spongiform Encephalopathies (TSE).
Ethylene oxide sterilization is a chemical process consisting of four primary variables: gas concentration, humidity, temperature and time. Ethylene oxide is an agent that disrupts the DNA of microorganisms, which prevents them from reproducing. ETO sterilization assures that a safe and sterile product will be delivered to the market each and every time.
Regulatory and Safety :- From last few year, the European Nerus and regulation enabled Medical Devices manufacturers to have dramatically improved the safety levels of Ethylene Oxide usage in indicated context to rationalize the ethylene oxide sterilization process while increasing its level of security.
Features : –
- Complete adherence to quality systems
- Use of Biological Indicators as basis of product release.
- Automatic sterilisation systems
- Customized process parameters and customer-specific support is available
