The requirement for safety testing of clinical laboratory medical equipment is regarded as essential to ensure that apparatus does not pose a user or patient hazard. John Backes, sales and product manager, Rigel Medical, considers the implications of the new IEC standard for the in-service and post-repair testing of electromedical devices.
Log in or register FREE to read the rest
This story is Premium Content and is only available to registered users. Please log in at the top of the page to view the full text.
If you don't already have an account, please register with us completely free of charge.