Single Use Device (SUD) Reprocessing

The hazardous practice known as single use device (SUD) reprocessing occurs when medical devices intended for single patient use are reprocessed, cleaned and sterilized, for repeated use.  According to the Association of Medical Device Reprocessors, since 2000 more than 55 million devices have been reprocessed and redistributed for multiple surgical usages. Single use devices are often reprocessed repeatedly, either until they fail or until multiple uses result in obvious wear.

In partnership with a global medical device manufacturer, OpSec has developed the only device that signals surgeons when a SUD has been reprocessed.  OpSec’s reprocess indicator label can be implemented on medical devices of various sizes and configurations.  Our indicator contains multiple layers of proprietary anti-counterfeit technology that prevents tampering and reproduction.  When the label is exposed to liquids that are used to clean devices, a covert message is rendered visible, warning the user of SUD reprocessing.