27 results
·
23ms
·
Sources: EU EUDAMED, US FDA
SILVERSEAL
FDA 510(k)
FDA Unclassified
·Unknown
Baltic Denture System BDLoad
FDA UDI
Merz Dental GmbH·D7091033587·Baltic Denture System BDLoad BDLoad ↓ Mm6 PLSEu...
BABIES BEST WATER TEETHER / GUM SOOTHER, VARIOUS
FDA 510(k)
FDA Class 2
·Dental
CLEARGLIDE PRECISION BIPOLAR DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 16, 2018
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 2, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 16, 2009
CLEARGLIDE EVH LONGVIEW W/SCIS
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 23, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 16, 2009
CLEARGLIDE EVH SMALL W/SCISSOR
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·October 16, 2009
CLEARGLIDE EVH LONGVIEW W/SCIS
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 9, 2009
USS NUT F/USS-VAR-AXIS-SCR USS-PEDICSCR+
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code NKB·April 3, 2013
BIOPSY GUIDE
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·February 11, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·April 23, 2008
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 24, 2009
CLEARGLIDE EVH SMALL W/SCISSOR
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 3, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 16, 2009