8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
UROLOGICAL CATHETERS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Fist Assist Devices Model FA-1
FDA 510(k)
FDA Class 2
·Physical Medicine
MEROX BIPOLAR HIGH IMPEDANCE LEAD MODELS: MEX 53/13-BP; 60/15-BP; 45-JBP; 53-JBP
FDA 510(k)
FDA Class 3
·Cardiovascular
BIOFLO DURAMAX
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS INC.·Product code MSD·April 25, 2025
TPRLC 133 MP TYPE1 PPS HO 11.0 5MM T1
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code KWA·November 22, 2019
XENFORM
FDA Adverse Event
Other
·TEI BIOSCIENCES INC.·Product code FTM·April 25, 2014
LYNX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·October 31, 2012
OT VERIO2 METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 2, 2015