10 results
·
26ms
·
Sources: EU EUDAMED, US FDA
CARDIOTHERM-500X
FDA 510(k)
FDA Class 2
·Cardiovascular
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293999·
NA
FDA UDI
KEY SURGICAL, INC.·10849771050060·Steinmann Pins, Single diamond, threaded, 0.177...
10PR - Premium - Poly Red
FDA UDI
Certified Safety Manufacturing, Inc.·00766588777184·10PR - Premium - Poly Red
STAIN, R-250, COOMASSIE BRILLIANT BLUE
FDA 510(k)
FDA Class 1
·Immunology
TRILOGY LONGEVITY CONSTRAINED LINER
FDA 510(k)
FDA Class 2
·Orthopedic
COCR FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·February 23, 2018
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·April 24, 2014
SYNCARDIA TEMPORARY TOTAL ARTIFICIAL HEART
FDA Adverse Event
Other
·SYNCARDIA SYSTEMS, INC.·Product code LOZ·September 10, 2012
BUTTON REPLACEMENT GASTROSTOMY DEVICE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code KNT·July 28, 2010