BEUDAMED
    12 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 Regulation: Us FDA ×

    PRIMAPORE I.V.

    FDA 510(k)
    FDA Class 1 ·General Hospital

    EDGELOCK

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GLUCOSE-6-PHOSPHATE DEHYDROGENASE

    FDA 510(k)
    FDA Class 2 ·Hematology

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 25, 2014

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code MMI·January 3, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Malfunction ·Product code KDJ·November 9, 2010

    SELECTSECURE MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVN·July 17, 2024

    ATTAIN STABILITY QUAD MRI SURESCAN

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code OJX·July 17, 2024

    SELECTSECURE MRI SURESCAN

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code NVN·July 17, 2024

    ATTAIN STABILITY QUAD MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code OJX·July 17, 2024

    1.5MM SYSTEM TWIST DRILL WITH J NOTCH 1.1 X 50MM, 15MM STOP

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HBE·July 9, 2020

    1.5MM SYSTEM TWIST DRILL WITH J NOTCH 1.1 X 50MM, 15MM STOP

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HBE·September 9, 2021