3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 23, 2012
6800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS SLC·Product code JAA·December 30, 2013
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 17, 2010