7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
ORTHODERM CONVERTIBLE
FDA 510(k)
FDA Class 2
·Physical Medicine
PHYSIOLOGICAL MONITOR 2100
FDA 510(k)
FDA Class 2
·Cardiovascular
OK FLASH STERILIZATION INDICATOR
FDA 510(k)
FDA Class 2
·General Hospital
FAST-CATH¿ HEMOSTASIS INTRODUCER, CATH-LOCK¿ LOCKING HUB, 12 CM SHEATH, 8.5 F
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code DYB·January 22, 2024
HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES, INC.·Product code LWR·November 3, 2010
OMNIPOD INSULIN PUMP
FDA Adverse Event
Malfunction
·INSULET CORPORATION·Product code LZG·November 16, 2012
COULTER LH 780 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·June 25, 2014