BEUDAMED
    6 results · 36ms · 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 ×

    BARCO INC

    FDA Adverse Event
    Malfunction ·BARCO INC·Product code FWB·December 16, 2021

    BARCO INC

    FDA Adverse Event
    Injury ·BARCO INC·Product code FWB·October 6, 2023

    DAVINCI SI

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·November 12, 2024

    VISIONPRO SYNK 26" WIRELESS LED DISPLAY INTERNATIONAL KIT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·November 28, 2023

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARCH, INC.·Product code FTL·February 7, 2012

    BARD CROSSER CTO RECANALIZATION CATHETER

    FDA Adverse Event
    Malfunction ·FLOWCARDIA, INC. A SUBSIDIARY OF BARC, INC.·Product code DQY·April 9, 2013