6 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
AQUAPHOR R GAUZE
FDA 510(k)
FDA Unclassified
·Unknown
Loss of Pulse Detection
FDA 510(k)
FDA Class 2
·Cardiovascular
A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512
FDA 510(k)
FDA Class 2
·Cardiovascular
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 13, 2014
INTERMATE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code FRN·November 21, 2012
ACCU-CHEK ® INFORM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·September 23, 2010