10 results
·
26ms
·
Sources: EU EUDAMED, US FDA
LATERALASE, MODIFIED
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
THROMBELASTOGRAPH
FDA 510(k)
FDA Class 2
·Hematology
EMIT QST ETHOSUXIMIDE ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
LIGASURE ADVANCE PISTOL GRIP
FDA Adverse Event
Malfunction
·COVIDIEN LP·Product code GEI·May 7, 2014
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 6, 2010
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 9, 2013
JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023
JAWS "HIQ+", 5 X 330 MM, SCISSORS, METZENBAUM
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·March 30, 2023
SHAFT "HIQ+", 5 X 330 MM
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·May 23, 2023
JAWS "HIQ+", 5 X 330 MM, GRASPING FORCEPS, CROCEOLMI
FDA Adverse Event
Malfunction
·OLYMPUS WINTER & IBE GMBH·Product code HET·March 15, 2023