BEUDAMED
    5 results · 19ms · 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 ×

    SUPREME EP CATHETER 5F, QUADRIPOLAR, JSN

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DRF·August 5, 2009

    X-FLOW PROSTATECTOMY CATHETER

    FDA Adverse Event
    Malfunction ·COLOPLAST A/S·Product code EZL·October 8, 2024

    SMARTLIFE LARGE ASEPTIC HOUSING

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS, INSTRUMENTS DIV.·Product code HWE·April 8, 2014

    SWARTZ BRAIDED TRANS. GUIDING INT., 8F, LAMP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, AF DIVISION·Product code DYB·October 11, 2012

    PROXIMATE** PLUS MD MULTI-DIRECTIONAL RELEASE SKIN STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDT·August 10, 2010