According to HIPAA, ePHI is, “any protected health information that is created, stored, transmitted, or received in any electronic format or media.” Any medical device which retains this information can prove to be a weakness in your facility’s defense of patient ePHI...
Evidence has been presented that semi-critical devices, devices that come in contact with mucous membranes or non-intact skin, such as endoscopes and endocavity probes, cause more healthcare associated infections than non-critical or critical medical devices...
Our CS Medical team receives a lot questions regarding Annual Device Verification, so we’ve put together a list of some of the most common concerns and their responses:
There are at least three solid reasons for making the change to automation and propelling your healthcare facility into the future.
Too many facilities have no standardized way of storing transesophageal echocardiogram (TEE) ultrasound probes. Some facilities have used transportation cases to store their TEE probes, but that is not their intended use and is actually prohibited in several countries.
