7 results
·
21ms
·
Sources: EU EUDAMED, US FDA
NEOTECH UNIVERSAL ADAPTER
FDA 510(k)
FDA Class 1
·Anesthesiology
JKH Stimulator Plus
FDA 510(k)
FDA Class 2
·Neurology
NUMERIS COAGULATION SYSTEM WITH VISITRAX, MODEL(S) CSK-021;CSK-022; CSK-023; CSK-025
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NUMERIS TETHERED COAGULATION SYSTEM WITH VISITRAX
FDA Adverse Event
Death
·ATRICURE, INC.·Product code OCL·November 13, 2018
SYSTEM 6 SAGITTAL SAW
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·June 18, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·October 25, 2010
TOTAL ASR FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD - 8010379·Product code KXA·December 20, 2012