BEUDAMED
    6 results · 21ms · 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 ×

    VESSEL DILATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TOPCON 3D OCT-1000 OPTICAL COHERENCE TOMOGRAPHY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    XPress BCD Breast Compression Device

    FDA 510(k)
    FDA Class 2 ·Radiology

    NONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 13, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 29, 2014

    VAPR ELECTRODE

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code GEI·January 14, 2011