BEUDAMED
    162 results · 59ms · 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.
    Filters FDA Adverse Event ×

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Death ·BIOSENSE WEBSTER (ISRAEL) LTD.·Product code DQK·March 2, 2017

    IMPELLA

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·April 20, 2026

    IMPELLA

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·April 2, 2026

    IMPELLA

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·March 12, 2026

    IMPELLA

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·March 18, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 9, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·May 20, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 11, 2026

    IMPELLA CPSA C9+ SET, OUS

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 11, 2026

    PURGE CASSETTE GEN 2, STERILE, NON QSK

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 9, 2026

    DAVINCI X

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·July 1, 2024

    AXILLARY INSERTION KIT

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code DYB·March 5, 2026

    PURGE CASSETTE GEN 2, STERILE, NON QSK

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·March 6, 2026

    IMPELLA CONTROLLER, PACKAGED, US

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·March 6, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 23, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·May 29, 2026

    IMPELLA

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·May 14, 2026

    IMPELLA

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·April 2, 2026

    TEMPORARY NON-ROLLER TYPE LEFT HEART SUPPORT BLOOD PUMP

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code OZD·March 31, 2026

    IMPELLA

    FDA Adverse Event
    Death ·ABIOMED, INC. - 1220648·Product code PYX·April 13, 2026