3 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MPRI·Product code DTB·June 10, 2014
8800
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·October 4, 2010
CUSTOMER CURVED QUICK-CONNECT
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS MAHWAH·Product code LXH·November 2, 2012