8 results
·
23ms
·
Sources: EU EUDAMED, US FDA
OLYMPIC LIGHT-WARM
FDA 510(k)
FDA Class 1
·General Hospital
PATIENT EXAMINATION GLOVES (LATEX)
FDA 510(k)
FDA Class 1
·General Hospital
MODELS 6526,6527,6528 PERCU. TRANS. ANGIO. CATH.
FDA 510(k)
FDA Class 2
·General Hospital
PRODISC-L REVISIONS
FDA Adverse Event
Injury
·SYNTHES·Product code MJO·January 4, 2013
ACCENT DR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·November 10, 2010
ARROW-TREROTOLA PTD KIT
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL, INC. (SUBSIDIARY OF TELEFLEX, INC.)·Product code MCW·June 17, 2014
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·May 17, 2023
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·June 26, 2023