BEUDAMED
    43 results · 27ms · 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.

    ENDOSCOPIC LIGHT SOURCE XL202/L3

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

    Mallinckrodt Medical

    FDA registration
    Mallinckrodt Medical·7 products·🇮🇪 Ireland

    SHILEY

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL·Product code JOH·September 6, 2018

    PNS MAGNETIC STIMULATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SENOJ IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    BRÅNEMARK SYSTEM MK III TIU RP 3.75X10MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·October 30, 2024

    NOBELACTIVE INTERNAL RP 4.3X11.5MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·October 30, 2024

    NOBELPARALLEL CC NP 3.75X11.5MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·November 4, 2024

    MALLINCKRODT

    FDA Adverse Event
    Injury ·MALLINCKRODT MEDICAL·Product code BTR·June 3, 2019

    MALLINCKRODT

    FDA Adverse Event
    Injury ·MALLINCKRODT MEDICAL·Product code BTR·June 4, 2019

    MALLINCKRODT

    FDA Adverse Event
    Injury ·MALLINCKRODT MEDICAL·Product code BTR·June 3, 2019

    NOBELPARALLEL CC NP 3.75X11.5MM

    FDA Adverse Event
    Malfunction ·NOBEL BIOCARE AB·Product code DZE·November 4, 2024

    PARAPAC 'MEDIC' (K020899)

    FDA Adverse Event
    Death ·SMITHS MEDICAL INTERNATIONAL·Product code BTL·August 6, 2004

    8020889-1999-00023

    FDA Adverse Event
    Malfunction ·December 11, 1999

    8020889-1999-00030

    FDA Adverse Event
    Malfunction ·December 31, 1999

    8020889-1999-00029

    FDA Adverse Event
    Malfunction ·December 31, 1999

    8020889-1999-00028

    FDA Adverse Event
    Malfunction ·December 22, 1999

    8020889-1999-00031

    FDA Adverse Event
    Malfunction ·December 31, 1999

    8020889-1999-00022

    FDA Adverse Event
    Malfunction ·December 11, 1999

    8020889-2018-00051

    FDA Adverse Event
    Malfunction ·MALLINCKRODT MEDICAL·Product code BTR·May 14, 2018