BEUDAMED
    13 results · 23ms · 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 Regulation: Us FDA ×

    ORTHODONTIC CERAMIC BRACKET

    FDA 510(k)
    FDA Class 2 ·Dental

    ULTRASOUND SCANNER TYPE 2102

    FDA 510(k)
    FDA Class 2 ·Radiology

    OPTIFLOW CATHETER #5641190 CATHETER ONLY #5643150 CATHETER KIT #5631000 CATHETERLESS TRAY-GENERIC (COMBINED WITH CATHETR

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

    VANGUARD M UNI FEMORAL LG

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code HRY·May 2, 2013

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·September 15, 2014

    XPRT SLEEP SURFACE

    FDA Adverse Event
    Malfunction ·STRYKER CORP DBA GAYMAR·Product code FNM·April 19, 2011

    BD TRUCOUNT TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·July 13, 2021

    BD TRUCOUNT TUBES

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code GKZ·July 15, 2021

    BD MULTITEST¿

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·February 9, 2024

    BD MULTITEST¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code GKZ·March 15, 2024

    BD MULTITEST¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·March 15, 2024

    BD MULTITEST¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD.·Product code GKZ·March 15, 2024

    BD TRUCOUNT¿ TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·May 2, 2025