7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
GMP CIQ ELISA TEST KIT
FDA 510(k)
FDA Class 2
·Immunology
MINI TIGHTROPE
FDA 510(k)
FDA Class 2
·Orthopedic
LIFEPAK 12, 20, 500, CR PLUS
FDA 510(k)
FDA Class 3
·Cardiovascular
LIFEPAK CR(R) PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·December 10, 2018
36MM COCR MOD HEAD +9MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·May 27, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·November 15, 2012
OLYMPUS RESECTION ELECTRODE
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 7, 2010