sterilisability
Sterilisability is the property of an item—such as a medical device, laboratory instrument, packaging material, or consumable—that describes its ability to undergo a validated sterilization process to achieve a defined level of sterility without compromising its function or integrity. In practice, sterilisability depends on the material composition, design features, and the compatibility of the item with the chosen sterilant and cycle.
Common sterilization methods include steam sterilization (moist heat in autoclaves), dry heat, ethylene oxide gas, hydrogen
Validation and quality assurance involve demonstrating that a sterilization process reliably achieves the desired sterility level,
Packaging and handling are integral to sterilisability, as improper packaging can compromise sterility or prevent the
In healthcare and laboratory settings, sterilisability informs selection, validation, and regulatory compliance to ensure patient and