BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    CIRCON ACMI GEN SURG INSTRU FOR MINI INVASIVE SURG

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    OPTYX

    FDA 510(k)
    FDA Class 2 ·Neurology

    LAPAROFLATOR ELECTRONIC 3509

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

    SYNCHRON (R) SYSTEMS CREATININE REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code CGX·July 2, 2011

    3002 SECURE II MED-SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·December 7, 2012

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code FKX·December 6, 2010

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·July 4, 2014

    BD BBL MGIT PANTA ANTIBIOTIC MIXTURE, LYOPHILIZED

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·February 4, 2021

    BD BBL¿ MGIT¿ OADC ENRICHMENT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 13, 2024

    BD BBL¿ MGIT¿ OADC

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·June 3, 2025

    BD BACTEC¿ MGIT¿ MYCOBACTERIA GROWTH INDICATOR TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·July 2, 2025

    BD BBL MGIT MYCOBACTERIA GROWTH INDICATOR TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·June 7, 2024

    BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·February 29, 2024

    BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·February 23, 2024

    BD BBL¿ MGIT¿ OADC

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·February 10, 2025