8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
DETERMIN. OF SALICYLATE IN SERUM/PLAST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
HISTOACRYL FLEXIBLE PACK 5
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code MPN·December 3, 2019
SHUNTONG
FDA 510(k)
FDA Class 1
·General Hospital
BARD ATLAS PTA BALLOON DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
CONTOUR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GDW·April 30, 2014
ADVIA CENTAUR CP VITAMIN B 12 ASSAY
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code CDD·November 20, 2012
IKARIA
FDA Adverse Event
Injury
·IKARIA·Product code MRN·September 14, 2010
VERSYS FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER, TURPEAUX INDUSTRIAL PARK·Product code JDI·March 31, 2016