27 results
·
44ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·March 1, 2012
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·April 14, 2014
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·March 6, 2012
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·March 6, 2012
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·March 12, 2014
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·March 10, 2014
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code JWH·June 28, 2013
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code JWH·June 28, 2013
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code JWH·June 28, 2013
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·October 28, 2011
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·October 21, 2011
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·October 21, 2011
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·October 21, 2011
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·November 30, 2011
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE N.V.·Product code MBH·August 8, 2012
PROPLAN CMF GUIDES
FDA Adverse Event
Malfunction
·MATERIALISE NV·Product code JEY·March 2, 2012
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE NV·Product code MBH·February 14, 2012
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE NV·Product code MBH·June 11, 2013
ZIMMER PATIENT SPECIFIC INSTRUMENT
FDA Adverse Event
Malfunction
·MATERIALISE NV·Product code MBH·June 11, 2013
TRUMATCH CMF
FDA Adverse Event
Malfunction
·MATERIALISE NV·Product code HWT·August 18, 2025