35 results · 35ms · Sources: EU EUDAMED, US FDA

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CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·October 22, 2024

MICRO INCISION VACUUM PACK

FDA Adverse Event
Injury ·BAUSCH & LOMB·Product code HQC·July 1, 2013

MICRO INCISION VACUUM PACK

FDA Adverse Event
Injury ·BAUSCH & LOMB·Product code HQC·July 1, 2013

MICRO INCISION VACUUM PACK

FDA Adverse Event
Injury ·BAUSCH & LOMB·Product code HQC·July 1, 2013

MICRO INCISION VACUUM PACK

FDA Adverse Event
Injury ·BAUSCH & LOMB·Product code HQC·July 1, 2013

MICRO INCISION VACUUM PACK

FDA Adverse Event
Injury ·BAUSCH & LOMB, INC.·Product code HQC·July 1, 2013

MICRO INCISION VACUUM PACK

FDA Adverse Event
Injury ·BAUSCH & LOMB·Product code HQC·July 1, 2013

CARDIOSAVE HYBRID, 3.1 EDITION

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·July 26, 2024

CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·December 21, 2023

IMPAX CV REPORTING

FDA Adverse Event
Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

FILTERWIRE EZ EMOBLIC PROTECTION SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - SAN JOSE·Product code NFA·February 24, 2011

ASCENSIA BREEZE2

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE, LLC·Product code NBW·February 15, 2008

CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·December 5, 2024

CARDIOSAVE HYBRID, TYPE G PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·November 23, 2025

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·April 14, 2018

CARDIOSAVE HYBRID, TYPE G PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·May 23, 2024

CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·November 11, 2025

CARDIOSAVE HYBRID TYPE D PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·January 30, 2024

HF SENSOR DELIVERY SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC. - CARDIOMEMS·Product code MOM·May 31, 2023

CHAIT PERCUTANEOUS CECOSTOMY CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KNT·June 16, 2023