BEUDAMED
    8 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.
    Filters Regulation: Us FDA ×

    TRIFIX PEDICLE SPINAL SCREW ASSEMBLY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SILHOUETTE SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Other ·CENTERPULSE SPINE-TECH·Product code MCV·November 14, 2003

    MODIFICATION TO: S4 SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STRETCHER TRANSIT ISOLATER #122

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RESERVOIR 1.8ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·March 5, 2013

    HEARTMATE II LVAD

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·February 8, 2011

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014

    NASAL-AIRE

    FDA Adverse Event
    Malfunction ·INNOMED TECHNOLOGIES·Product code BYE·January 6, 2003