BEUDAMED
    6 results · 17ms · 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.

    PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO

    FDA 510(k)

    DPX-L AND DPX-ALPHA, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    HEX, QUAD, OR RAIL BLOCK MANIFOLD ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PINNACLE MTL INS NEUT40IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·February 11, 2013

    RF3000 RADIOFREQUENCY GENERATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SAN JOSE·Product code GEI·July 24, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011