BEUDAMED
    7 results · 25ms · 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 ×

    ANGIO-SEAL DEVICE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL PUERTO RICO, B.V.·Product code MGB·November 14, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 16, 2011

    PWRD ECH FLEX 45MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 29, 2013

    BLUNT TIP SCREW, ÿ 4X46MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·October 28, 2024

    VISTASEAL DUAL APPLICATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code MZM·October 10, 2025

    VISTASEAL DUAL APPLICATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code MZM·July 8, 2025

    GEM MICROVASCULAR ANASTOMOTIC COUPLER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code MVR·August 21, 2025