BEUDAMED
    7 results · 34ms · 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 ×

    UNKNOWN_MEDICAL_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·May 27, 2014

    HUDSON/MODIFIED TRINKLE ATTACH

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·November 7, 2012

    X-SMART

    FDA Adverse Event
    Injury ·DENTSPLY MAILLEFER·Product code EKX·September 9, 2010

    BD SYRINGE 10ML REG PR SALINE FILL SPKG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·August 12, 2020

    BD POSIFLUSH SF SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·September 10, 2020

    BD POSIFLUSH XS PRE-FILLED FLUSH SYRINGE NACL 0.9%

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·September 15, 2020

    BD POSIFLUSH SF SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND CO.·Product code NGT·January 15, 2021