8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
POLYFLEX 483-09 ENDOCARDIAL IMPLANTABLE PACINGLEAD
FDA 510(k)
FDA Class 3
·Cardiovascular
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209125647·
ARTHROSCAN VIDEO SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
TA-201 CLINICAL AUDIOMETER
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
INTER-LOCK SCREWDRIVER T25/3.5MM HEX/224MM
FDA Adverse Event
Malfunction
·SYNTHES HAGENDORF·Product code HXX·March 21, 2016
PINN MAR NEUT 28IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 6, 2014
PARALLAX ACRYLIC RESIN WITH TRACERS
FDA Adverse Event
Death
·NEUROTHERM·Product code NDN·November 29, 2012
FLUOROSTAR
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·September 2, 2010