6 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
LATEX PATIENT EXAMINATION GLOVE (POWDERFREE/HYPOALLERGENIC) (MODIFICATION)
FDA 510(k)
FDA Class 1
·General Hospital
BUECHEL-PAPPAS HUMERAL STEM COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
RADIATION BEAM DATA ACQUISTIOIN SYSTEMS
FDA 510(k)
FDA Class 2
·Radiology
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MPRI·Product code DTB·February 11, 2013
DURATA STS OPTIM ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 16, 2014