9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
CONPHAR AIRWAYS
FDA 510(k)
FDA Class 1
·Anesthesiology
ACA ALCOHOL CALIBRATORS
FDA 510(k)
FDA Class 2
·Clinical Toxicology
CABLE READY CABLE GRIP SYSTEM CABLE BUTTON
FDA 510(k)
FDA Class 2
·Orthopedic
YSI MODEL 791/799 DISP TEMP PROBE & 7900 EX CABLE
FDA 510(k)
FDA Class 2
·General Hospital
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 6, 2014
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·October 15, 2012
ISERT ASPHERIC INTRAOCULAR LENS
FDA Adverse Event
Malfunction
·HOYA SURGICAL OPTICS, INC.·Product code HQL·August 4, 2010
INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, LUMBAR
FDA Adverse Event
Injury
·SYNTHES USA·Product code MAX·November 18, 2015
INTERVERTEBRAL FUSION DEVICE WITH INTEGRATED FIXATION, LUMBAR
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code OVD·November 18, 2015