27 results · 23ms · Sources: EU EUDAMED, US FDA

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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