BEUDAMED
    9 results · 22ms · 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 FDA Adverse Event ×

    DANEK PLATE AND SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code KWQ·February 19, 1999

    BD ALLERGY SYRINGE TRAY WITH BD SAFETYGLIDE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code MEG·August 15, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·HUDSON OXYGEN THERAPY SALES·Product code CAT·July 1, 1992

    EFFERGRIP DENTURE ADHESIVE CREAM

    FDA Adverse Event
    Injury ·JOHNSON AND JOHNSON GROUP OF CONSUMER COMPANIES·Product code KOL·December 4, 2008

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 16, 2011

    RESTORE ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 29, 2013

    ATHENA PATIENT MONITORING SYSTEM - ADULT

    FDA Adverse Event
    Injury ·S & W MEDICO TEKNIK-ALBERTSLUND, DENMARK·Product code KMI·January 21, 1992

    AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·June 6, 2013

    AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·July 11, 2013