9 results
·
29ms
·
Sources: EU EUDAMED, US FDA
CERAMIC ORTHODONIT APPLIANCE
FDA 510(k)
FDA Class 1
·Dental
NAR Kit
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209107735·KIT, VEHICLE TRAUMA RESPONSE (V-TRK)
CARDIOSCOPE J200
FDA 510(k)
FDA Class 2
·Cardiovascular
GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive Only; GEM Flex Coil 16-S Array, 1.5T Receive Only
FDA 510(k)
FDA Class 2
·Radiology
PINNACLE MTL INS NEUT40IDX58OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·October 30, 2013
12/14 ARTICUL 40MM M SPEC+1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·October 30, 2013
DETACHATIP MULTI-USE GRASPERS, BLUNT NOSE DISSECTOR, 5MMX 33CM
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code GEI·June 5, 2014
LIBERTY CYCLER SET, SINGLE CONN./EXT. DL
FDA Adverse Event
Malfunction
·REYNOSA MFG·Product code FKX·November 12, 2012
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 29, 2010