Following superbug outbreaks after issues with reprocessing certain medical devices, the US Food and Drug Administration (FDA) on Thursday released a list of devices that the agency will require ...
The US Food and Drug Administration’s (FDA) Center for Devices and Radiological Health (CDRH) recently warned two foreign medical device companies – a manufacturer of microcatheters and a laparoscopic ...
The latest interim results from US Food and Drug Administration (FDA)–mandated postmarket surveillance studies of duodenoscopes continue to show unacceptably high contamination rates after ...
It might surprise you that Europe, and specifically the European Union (EU), is lagging far behind the United States when it comes to the re-use of single-use devices. After all, Europe is usually ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results