What is the FDA and what does it even mean to say that a product has been cleared for use by the FDA and how is such clearance obtained?
In this age of instant information at our fingertips, technologies that retain all information on a patient procedure and make it easily transportable via thumb drive are very attractive. But are they compliant with laws and standards set by HIPAA and by accrediting agencies, like TJC?
When you’re considering purchasing an automated TEE ultrasound probe reprocessor for your facility. At CS Medical, we recognize that every facility has different preferences and needs, so we provide several state of the art options to take into consideration:
As you have been thinking about or reviewing existing SOP’s (Standard Operating Procedures), a key factor that is important to always remember is your staff and the complex job they are tasked to complete.
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...
Do we have any reason to believe our water is always safe for consumption? More importantly, do we know that our municipal water is safe for rinsing semi-critical devices, like TEE probes and endoscopes, so as to retain high-level disinfection status?
Are you prepared to provide records of every single cleaning, disinfection, and maintenance event for your TEE probes?
When reprocessing transesophageal echocardiogram (TEE) ultrasound probes, sometimes the numerous steps can feel overwhelming