BEUDAMED
    9 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.

    C.L.A.T.

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981124106·18x15x8mm, 7 Degree, No Profile Integrated Spacer

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·00889981124109·No Profile Spacer, 18x15x8mm, 7 Degree, Sterile

    THERMAL CAUTERY PROBE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Palm TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    NIM-ECLIPSE® CONTROLLER

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code GWF·December 9, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 15, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·November 26, 2012

    LENSX LASER SYSTEM

    FDA Adverse Event
    Injury ·ALCON LENSX, INC.·Product code OOE·June 17, 2015