BEUDAMED
    8 results · 20ms · 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 ×

    M.U.S.T. Sacral Illiac Screw and Pelvic Trauma System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRULY AUTOMATIC ARM BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AGILIS ES STEERABLE INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CONTINUUM KNEE

    FDA Adverse Event
    Malfunction ·ZIMMER TMT·Product code HSH·October 2, 2008

    ECHELON*FLEX60 LONG

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 27, 2013

    PENTA 60-CM LENGTH PADDLE LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 21, 2011

    HANDLE ACETABULAR PRESS

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025

    ACETABULAR PRESSURIZER SMALL

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LXH·May 23, 2025