Medical Device Reporting Software
2 software items found
-
based in USA
The medical device reporting (MDR) requirements of 21 CFR 803 apply to manufacturers, importers, distributers, and device user facilities in the United States. Such facilities are required to report adverse device-related events to the Food and Drug Administration (FDA) or the ...
-
Manufactured by Cisa Group S.R.L.based in ITALY
. The communication between TraceCare® and the PLC of the machines is unidirectional, so the system is able to read information from the machines but cannot send commands, thus protecting from possible alterations to the medical devices. ...
Need help finding the right suppliers? Try XPRT Sourcing. Let the XPRTs do the work for you