7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Minuteman G5 MIS Fusion Plate; Minuteman G1(Posterior Fusion Plate /HA Posterior Fusion Plate); HA Minuteman G3-R MIS Fusion Plate; Minuteman G3/HA Minuteman G3
FDA 510(k)
FDA Class 2
·Orthopedic
BD NEXIVA 22 GA X 1.00IN SP WITH MAXZERO
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 29, 2023
DYNATRAC, COD. 50-1A
FDA 510(k)
FDA Class 2
·Radiology
TRANSONIC ELSA SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code NIQ·November 4, 2008
UNKNOWN PRODUCT- CERAMIC ON CERAMIC HIP
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CORK·Product code MEH·August 29, 2011
CORDLESS DRIVER 3
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code HRX·July 18, 2013