BEUDAMED
    6 results · 33ms · 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.

    PERNECZKY CLIP APPLIER/REMOVER

    FDA 510(k)
    FDA Class 2 ·Neurology

    CHURCHILL - HBC VENTED BALL CHECK IV SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AUTOMATED DISPOSABLE SOFT TISSUE BIOPSY ASPIR. DEV

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

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·February 11, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·January 10, 2011

    SIENTRA SILICONE GEL-FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·SIENTRA, INC·Product code FTR·July 18, 2014