7 results
·
17ms
·
Sources: EU EUDAMED, US FDA
IMMUNODOT RUBELLA TEST
FDA 510(k)
FDA Class 2
·Microbiology
Snowden-Pencer
FDA UDI
STERIS CORPORATION·10885403153112·Snowden-Pencer ENDOPLASTIC DISSECTOR 8, 9-3/4 i...
DEFIB-PADS
FDA 510(k)
FDA Class 2
·Cardiovascular
PROPHY CARE SOLUTION
FDA 510(k)
FDA Class 1
·Dental
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Injury
·DEXCOM, INC.·Product code MDS·June 19, 2014
PD CYCLER 110 VOLT HOMECHOICEPRO AUTOMATED
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·October 28, 2010
RESTORIS MULTICOMPARTMENTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MAKO SURGICAL·Product code HAW·December 11, 2012