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

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CENTRIMAG BLOOD PUMP, CAN

FDA Adverse Event
Injury ·THORATEC SWITZERLAND GMBH·Product code QNR·March 30, 2026

ROTAFLOW 2-PUMPS CONSOLE

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DTQ·May 28, 2015

CENTRIMAG BLOOD PUMP, CAN

FDA Adverse Event
Injury ·THORATEC SWITZERLAND GMBH·Product code QNR·May 31, 2026

CENTRIMAG BLOOD PUMP, CAN

FDA Adverse Event
Injury ·THORATEC SWITZERLAND GMBH·Product code QNR·May 31, 2026

CENTRIMAG BLOOD PUMP, CAN

FDA Adverse Event
Injury ·THORATEC SWITZERLAND GMBH·Product code QNR·May 31, 2026

CENTRIMAG BLOOD PUMP, CAN

FDA Adverse Event
Injury ·THORATEC SWITZERLAND GMBH·Product code QNR·March 30, 2026

A.M.G. PMP PEDIATRIC STE CA

FDA Adverse Event
Injury ·EUROSETS S.R.L.·Product code DTZ·March 30, 2026

A.M.G. PMP PEDIATRIC STE CA

FDA Adverse Event
Injury ·EUROSETS S.R.L.·Product code DTZ·March 26, 2026

CENTRIMAG BLOOD PUMP, CAN

FDA Adverse Event
Injury ·THORATEC SWITZERLAND GMBH·Product code KFM·March 26, 2026

HLM TUBING SET W/BIOLINE COATING

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DTZ·April 24, 2015

QUADROX-ID AD.O.FIL.

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DTZ·December 9, 2014

HLS SET ADVANCED 7.0

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·November 24, 2020

HLS SET ADVANCED 7.0

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY GMBH·Product code DTZ·November 4, 2020

CUSTOM TUBING PACK

FDA Adverse Event
Injury ·DATASCOPE CORP·Product code DTL·July 28, 2015

QUADROX-ID

FDA Adverse Event
Injury ·MAQUET CARDIOPULMONARY AG·Product code DTZ·October 17, 2014

UNKNOWN DISTRIBUTED DIALYZER

FDA Adverse Event
Injury ·*·Product code FJI·April 24, 1996

EVOKE SCS SYSTEM

FDA Adverse Event
Injury ·SALUDA MEDICAL PTY LTD·Product code LGW·October 10, 2023

UNKNOWN DISTRIBUTED DIALYZER

FDA Adverse Event
Injury ·*·Product code FJI·April 24, 1996

UNKNOWN DISTRIBUTED DIALYZER

FDA Adverse Event
Injury ·*·Product code FJI·April 24, 1996

TERUMO TAF175 (HF/CR/1.75/M)

FDA Adverse Event
Injury ·TERUMO CORP·Product code FJI·April 24, 1996