BEUDAMED
    6 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.

    ENZYGNOST + ANTI-CMV IGG TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Vaccess™ CT Low-Profile Power-Injectable Implantable Port; Vaccess™ CT Power-Injectable Implantable Port; PowerPort™ duo M.R.I. ™ Implantable Port

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MFCD 1219, MFCD 1219 TS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 5, 2014

    *

    FDA Adverse Event
    Injury ·ARROW INTERNATIONAL, INC. (SUBSIDIARY OF TELEFLEX, INC·Product code DQX·November 15, 2012

    OCTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 30, 2010