8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
TXIT D.A.U. BARBITURATE ASSAY (MODIFICATION)
FDA 510(k)
FDA Class 2
·Clinical Toxicology
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113171·PS Insert, Size 3 x 14mm
DIGI-PRO TENS, MODEL WL-2204 AND WL-2205
FDA 510(k)
FDA Class 2
·Physical Medicine
WELLDOC DIABETES MANAGER SYSTEM AND DIABETES MANAGER RX SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·April 29, 2016
DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 16, 2015
FREESTYLE
FDA Adverse Event
Injury
·Product code NBW·December 10, 2010
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·December 17, 2012