8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
INSTATEMP
FDA 510(k)
FDA Class 2
·General Hospital
ANGIOGRAPHIC GUIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
LCD Monitor (MD310C, MD310G, MD210G)
FDA 510(k)
FDA Class 2
·Radiology
THRUWAY GUIDE WIRES
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·March 7, 2011
LOGIC TIBIA IMPLANT PSC INSERT, SZ 4, 11MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·July 5, 2023
CODMAN* DISP PERFORATOR
FDA Adverse Event
Injury
·Product code HBF·April 24, 2014
PROMUS ELEMENT ¿
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 3, 2012
DYNAMIC COMPRESSION CABLE PLATE SS 9 HOLE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDQ·July 27, 2010