13 results · 21ms · 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.

ENDOPATH ETS

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·November 7, 1997

RU NOVOSIBIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013

ST JOSEPHS PHOENIX, AZ 1

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code DWF·July 31, 2009

RU NOVOSIBRIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013

RU NOVOSIBIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DWF·October 16, 2013

CP87170 DE MUENCHEN

FDA Adverse Event
Death ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code OSI·April 16, 2013

MICROCAPS ARTHROWAND

FDA Adverse Event
Other ·ARTHROCARE CORP.·Product code GEI·June 18, 2008

HOMECHOICE AUTOMATED PD SET WITH CASSETTE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 18, 2011

CP87641 GB SOUTHAMPTON

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DWE·March 22, 2010

SITE-RITE 8 ULTRASOUND SYSTEM 20MM PINPOINT GT PROBE (REMANUFACTURED)

FDA Adverse Event
Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code IYO·November 9, 2022

ENDOPATH ETS FLEX

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·February 6, 1998

D 100 PH.I.S.I.O. NEWBORN HOLLOW FIBER MEMBRANE OXYGENATOR WITH RESERVOIR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code DTZ·March 28, 2017