BEUDAMED
    7 results · 18ms · 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.

    MODEL 109 SERIES BLOOD PRODUCTS IRRADIATORS

    FDA 510(k)
    FDA Unclassified ·Unknown

    SUNGLASSES-NONPRESCRIPTION INCLUDING PHOTOSEN.

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    DRAINAGE TUBE RESTRAINT/WOUND COVER

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTMES INC.·Product code LZG·November 29, 2010

    SYMMETRY SR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 15, 2014

    INTOUCH

    FDA Adverse Event
    Injury ·STRYKER MEDICAL·Product code FNL·December 7, 2012

    BD BACTEC FX, INSTRUMENT TOP, PACKAGED

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·February 22, 2021