8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
SURGICAL PROCEDURE TRAY/LAPAROSCOPY CHOLECYSTECTOM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MICROMAX(TM) INSTRUMENT CASE
FDA UDI
Biomet Orthopedics, LLC·00880304438637·
DS60 TOOTHBRUSH SANITIZER
FDA 510(k)
FDA Class 1
·Dental
APPLICARD (EKG)
FDA 510(k)
FDA Class 2
·Cardiovascular
ENERGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 9, 2013
TAXUS (R) LIBERTÉ (R)
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 23, 2010
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 1, 2014
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·September 1, 2022