9 results
·
18ms
·
Sources: EU EUDAMED, US FDA
NURSE'S AID PATIENT ROTATION SYSTEM
FDA 510(k)
FDA Class 2
·Physical Medicine
MODULAR FOOT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ORIGIO® Handling without phenol red (Cat. No. 8310), ORIGIO® Handling with phenol red (Cat. No. 8311)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 19, 2013
TRUFILL DCS ORBIT MINI COMPLEX FILL
FDA Adverse Event
Malfunction
·CORDIS NEUROVASCULAR, INC.·Product code HCG·January 31, 2011
SYNCHROMED EL
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code LKK·August 1, 2014
COULTER ACT PAK REAGENT KIT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·September 24, 2014
COULTER ACT PAK REAGENT KIT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·May 26, 2015
COULTER ACT PAK REAGENT KIT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·May 5, 2015