7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BERA SH 221 BRIAN STEM AUDIOMETER
FDA 510(k)
FDA Class 1
·Microbiology
SONOSITE MAXX SERIES ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Servo-air Lite Ventilator System
FDA 510(k)
FDA Class 2
·Anesthesiology
POWERPACK
FDA Adverse Event
Malfunction
·ICC-NEXERGY·Product code IYN·September 3, 2013
COUGAR XT HYDRO TRACT GUIDE WIRE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DQX·November 6, 2012
DUROM US ACETABLILAR COMPONENT 48/42 H
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·March 26, 2014
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·September 1, 2010