7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Blood Pressure Monitor (B73, BE23T)
FDA 510(k)
FDA Class 2
·Cardiovascular
19-INCH (48 CM) COLOR LCD MONITOR CDL1902A
FDA 510(k)
FDA Class 2
·Radiology
The UltraPulse system (UltraPulse and UltraPulse DUO models,members of the modified Lumenis Family of UltraPulse SurgiTouch
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SCISSORS, BLUNT, 5 FR., 34 CM
FDA Adverse Event
Malfunction
·KARL STORZ SE & CO. KG·Product code GCJ·July 31, 2025
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·December 3, 2008
ENDEAVOR SPRINT RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·September 13, 2011
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013