14 results · 56ms · Sources: EU EUDAMED, US FDA

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i3 Membrane GmbH

FDA registration
i3 Membrane GmbH·1 product·🇩🇪 Germany

EXCOR BLOOD PUMP PU VALVES, 15 ML IN/OUT Ø9 MM

FDA Adverse Event
Malfunction ·BERLIN HEART GMBH·Product code DSQ·March 9, 2018

EXCOR BLOOD PUMP PU VALVES, 15 ML IN/OUT Ø9 MM

FDA Adverse Event
Malfunction ·BERLIN HEART GMBH·Product code DSQ·December 21, 2018

EXCOR BLOOD PUMP PU VALVES, 25 ML IN/OUT Ø9MM

FDA Adverse Event
Malfunction ·BERLIN HEART GMBH·Product code DSQ·March 9, 2018

EXCOR®

FDA Adverse Event
Malfunction ·BERLIN HEART GMBH·Product code DSQ·October 17, 2025

EXCOR BLOOD PUMP PU VALVES, 25ML IN/OUT Ø9MM

FDA Adverse Event
Malfunction ·BERLIN HEART GMBH·Product code DSQ·June 21, 2016

EXCOR BLOOD PUMP PU VALVES, 25 ML IN/OUT Ø9 MM

FDA Adverse Event
Malfunction ·BERLIN HEART GMBH·Product code DSQ·June 7, 2019

BLOOD PUMP PU VALVES 25 ML, IN/OUT Ø9 MM

FDA Adverse Event
Injury ·BERLIN HEART GMBH·Product code DSQ·March 11, 2024

BLOOD PUMP PU VALVES 30 ML, IN/OUT Ø9 MM

FDA Adverse Event
Injury ·BERLIN HEART GMBH·Product code DSQ·March 11, 2024

HLM TUBING SET W/BIOLINE COATING

FDA Adverse Event
Death ·MAQUET CARDIOPULMONARY AG·Product code DWE·February 11, 2019

TUBING SETS

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DWE·March 13, 2025

BLOOD PUMP PU VALVES 30 ML, IN/OUT Ø9 MM

FDA Adverse Event
Injury ·BERLIN HEART GMBH·Product code DSQ·April 15, 2024

BLOOD PUMP PU VALVES 15 ML, IN/OUT Ø9 MM

FDA Adverse Event
Injury ·BERLIN HEART GMBH·Product code DSQ·April 23, 2024

Maquet Cardiopulmonary GmbH / Getinge Quadrox-iD Pediatric Diffusion Membrane Oxygenator with Bioline Coating, Sterile REF: BEQ-HMOD 30000

FDA Recall
Open, Classified ·GETINGE US SALES LLC·Product code DTZ·November 13, 2019