175 results · 24ms · Sources: EU EUDAMED, US FDA

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NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·April 8, 2011

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·August 30, 2013

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·November 16, 2010

ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

FDA Adverse Event
Injury ·COOK INC·Product code MIH·December 1, 2010

PUREFLOW SL

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KPO·July 30, 2008

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·July 7, 2014

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·October 19, 2012

DIALYSATE SACK WITH CONCENTRATE (SAK-302)

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KPO·March 7, 2023

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·October 23, 2009

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·April 18, 2014

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code FKR·May 5, 2023

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·April 17, 2014

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·August 7, 2018

ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAT·August 7, 2018

SYNVISC ONE

FDA Adverse Event
Injury ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·June 8, 2018

NXSTAGE SYSTEM ONE

FDA Adverse Event
Injury ·NXSTAGE MEDICAL, INC.·Product code FII·July 27, 2007

VALIANT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·October 1, 2014

BAK VISTA INTERBODY FUSION SYS

FDA Adverse Event
Injury ·ZIMMER·Product code MAX·December 28, 2014

BAK/CERVICAL (BAK/C)

FDA Adverse Event
Injury ·SULZER SPINE TECH·Product code MAX·July 21, 2003

BAK/CERVICAL (BAK/C)

FDA Adverse Event
Injury ·SULZER SPINE TECH·Product code MAX·June 4, 2003