7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
UNIVERSAL STERNUM SPREADER AND I.M.A. RETRACTOR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Panther Fusion GBS Assay
FDA 510(k)
FDA Class 1
·Microbiology
CADD MEDICATION CASSETTE RESERVOIR
FDA 510(k)
FDA Class 2
·General Hospital
CADD MEDICATION CASSETTE
FDA Adverse Event
Malfunction
·NULL·Product code FPA·February 4, 2022
TERUMO VIRTUOSAPH VEIN HARVESTING SYSTEM
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·October 1, 2010
RIATA ACTIVE FIXATION LEAD
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code LWS·January 13, 2014
EON
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 14, 2012