7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
MYODAC
FDA 510(k)
FDA Class 2
·Neurology
QIAstat-Dx Respiratory Panel
FDA 510(k)
FDA Class 2
·Microbiology
SONOWAND INVITE
FDA 510(k)
FDA Class 2
·Neurology
6461500 INFUSOR PUMP (1 LABEL)
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 11, 2010
UNICEL® DXC 600 PRO SYNCHRON® CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·October 26, 2010
OT DELICA LANCING DEVICE
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 21, 2012
TANDEM T:SLIM INSULIN DELIVERY SYSTEM
FDA Adverse Event
Injury
·TANDEM DIABETES·Product code LZG·June 9, 2014