8 results
·
24ms
·
Sources: EU EUDAMED, US FDA
IMPLANT PACING LEAD TINED #3390, MODIFICATION
FDA 510(k)
FDA Class 3
·Cardiovascular
Novo Surgical
FDA UDI
NOVO SURGICAL, INC.·G5869132030·osteotome caps, gas or steam permeable, latex-f...
SONY LMD-2451MT LCD MONITOR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BIOSCANNER BEYOND GLUCOSE ANALYZER AND TEST STRIPS
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CONSULT HCG TEST
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code JHI·March 4, 2025
MAXI MOVE
FDA Adverse Event
Injury
·ARJOHUNTLEIGH MAGOG INC·Product code FSA·June 10, 2014
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 14, 2013
RECONSTITUTION DEVICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MALTA·Product code FRN·December 2, 2010