8 results
·
17ms
·
Sources: EU EUDAMED, US FDA
OREX ISOLATION GOWN
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PACING/PSI KIT: 5 FR/6 FR 2-L
FDA Adverse Event
Malfunction
·ARROW INTERNATIONAL INC.·Product code LDF·April 15, 2015
METAL ENCLOSED SIDE FIRING FIBERS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OCTA-HEX (TM) IMPLANT RESTORATION SYSTEMS
FDA 510(k)
FDA Class 2
·Dental
FOOTSWITCH 1895420 XPS MULTIFUNCTIONAL
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED, INC.·Product code ERL·January 31, 2013
PHASEAL INFUSION ADAPTER
FDA Adverse Event
Malfunction
·CARMEL PHARMA AB.·Product code FPA·December 21, 2010
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·July 18, 2014
Bio-Rad brand ''TOX/See Drug Screen Test''; Catalog numbers: 1945182EX, 1945216, 194-5223
FDA Recall
Terminated
·Bio-Rad Laboratories Inc·Product code DIO·June 4, 2004