58 results · 22ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SENSTION PLUS 7.SFR 40CC INTRA AORTIC BALLOON CATHETER

FDA Adverse Event
Death ·GETINGE / DATASCOPE CORP.·Product code DSP·February 25, 2021

SOLITAIRE FR

FDA Adverse Event
Death ·COVIDIEN·Product code NRY·January 6, 2015

SOLITAIRE FR

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·December 20, 2024

SOLITAIRE FR

FDA Adverse Event
Death ·COVIDIEN (IRVINE)·Product code NRY·May 17, 2018

SOLITAIRE FR

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·August 7, 2024

PREMICATH 1FR PICC

FDA Adverse Event
Death ·VYGON CORP.·Product code LJS·April 7, 2014

ST JUDE VICTORY MODEL 5816

FDA Adverse Event
Death ·ST JUDE MFR·Product code DXY·March 11, 2009

WHIRLPOOL

FDA Adverse Event
Death ·ARJO MFR CO·Product code ILJ·September 22, 1995

PREMICATH

FDA Adverse Event
Death ·VYGON GMBH·Product code LJS·July 29, 2021

ACCU-CHEK COMFORT CURVE

FDA Adverse Event
Death ·ROCHE DIAGNOSTICS·Product code CFR·January 15, 2004

SURESTEP

FDA Adverse Event
Death ·LIFESCAN, INC.·Product code CFR·March 5, 2002

METER C - OT PROFILE

FDA Adverse Event
Death ·LIFESCAN, INC.·Product code CFR·February 20, 2002

PRECISION PCX

FDA Adverse Event
Death ·MEDISENSE, INC·Product code CFR·March 27, 2002

PRECISION XTRA MONITOR

FDA Adverse Event
Death ·MEDISENSE, INC.·Product code CFR·February 26, 2002

ACCU-CHEK COMFORT CURVE

FDA Adverse Event
Death ·ROCHE DIAGNOSTICS·Product code CFR·March 14, 2002

ACCU-CHEK ADVANTAGE

FDA Adverse Event
Death ·ROCHE DIAGNOSTICS·Product code CFR·December 5, 2003

PRECISION QID GLUCOSE METER

FDA Adverse Event
Death ·MEDISENSE, INC.·Product code CFR·August 7, 2000

ACCU-CHEK COMFORT CURVE

FDA Adverse Event
Death ·ROCHE DIAGNOSTICS·Product code CFR·June 9, 2000

ONE TOUCH BASIC

FDA Adverse Event
Death ·LIFESCAN, INC.·Product code CFR·May 19, 2000

ONE TOUCH II

FDA Adverse Event
Death ·LIFESCAN, INC.·Product code CFR·May 30, 2000