BEUDAMED
    38 results · 51ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    RAINDROP NEAR VISION INLAY

    FDA Adverse Event
    Malfunction ·REVISION OPTICS, INC.·Product code LQE·October 29, 2017

    RAINDROP NEAR VISION INLAY

    FDA Adverse Event
    Malfunction ·REVISION OPTICS, INC.·Product code LQE·October 20, 2017

    RAINDROP NEAR VISION INLAY

    FDA Adverse Event
    Malfunction ·REVISION OPTICS, INC.·Product code LQE·September 20, 2017

    FUSED LIGHT CABLE, 5.0 MM X 274CM (9.0')

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FST·May 20, 2024

    IMPELLA

    FDA Adverse Event
    Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·April 30, 2026

    FUSED LIGHT CABLE, 5.0 MM X 274CM (9.0')

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FST·June 18, 2024

    UNK

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FST·June 17, 2024

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 1, 2016

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 8, 2016

    FUSED LIGHT CABLE, 5.0 MM X 274CM (9.0')

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FST·May 30, 2024

    4K LAPAROSCOPE, 30 DEG, 10 X 330MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·June 18, 2024

    4K LAPAROSCOPE, 30 DEG, 10 X 330MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·June 5, 2024

    4K SYNERGYID CAMERA HEAD, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·May 10, 2024

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING NETHERLANDS·Product code HQL·March 28, 2023

    4K LAPAROSCOPE, 30 DEG, 10 X 330MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·June 10, 2024

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·October 6, 2016

    FUSED LIGHT CABLE, 5.0 MM X 274CM (9.0')

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FST·June 18, 2024

    4K LAPAROSCOPE, 30 DEG, 10 X 330MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code GCJ·June 7, 2024

    O-ARM 1000 IMAGING SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 7, 2016

    FUSED LIGHT CABLE, 5.0 MM X 274CM (9.0')

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code FST·May 22, 2024