6 results
·
25ms
·
Sources: EU EUDAMED, US FDA
DATA TERMINAL MODEL 722
FDA 510(k)
FDA Class 1
·Clinical Chemistry
VesoFlow Lite DVT Compression Device
FDA 510(k)
FDA Class 2
·Cardiovascular
HY-TEC SPECIFIC AND TOTAL IGE EIA SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
PRECISION®
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 30, 2014
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FPA·October 10, 2012
REPLY DR
FDA Adverse Event
Malfunction
·SORIN BIOMEDICA CRM S.R.L.·Product code DXY·August 3, 2010