BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    INTRASTENT DOUBLESTRUT LD

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SERIES 2000 ADJUSTABLE BED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GLENVEIGH VAGINAL TAMPONADE BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CIAGLIA BLUE RHINO PERCUTANEOUS TRACHEOSTOMY INTRODUCER SET WITH SHILEY

    FDA Adverse Event
    Injury ·COOK INC·Product code JOH·January 31, 2019

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 1, 2013

    PULSE GEN MODEL 103

    FDA Adverse Event
    Death ·CYBERONICS, INC.·Product code LYJ·February 11, 2011

    CAPSUREFIX

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014

    Daig Livewire Steerable, Product Number 401915; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026