BEUDAMED
    6 results · 28ms · 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 Regulation: Us FDA ×

    SYNCHRON SYSTEMS DAT LOW AND HIGH URINE CONTROLS 1

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    MODIFICATION OF MONO-PLUS(TM)

    FDA 510(k)
    FDA Class 2 ·Immunology

    COHERENT MARIE ARGON PHOTOCOAGULATOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SMARTSITE EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·June 25, 2014

    IDENTITY ADX XL DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·February 28, 2013

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·February 3, 2011