BEUDAMED
    7 results · 41ms · 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 ×

    THE UNIVERSAL BONE CEMENT RESISTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CENTURY SERIES HOLTER SCANNER SYSTEM, MODELS C3000, C2000 AND C1000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CERVICAL PASSIVE MOTION

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    CART 9734056 S7 STAFF SHRT 100-120V INTL

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·August 13, 2024

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 22, 2013

    CAPSURE Z

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    UNKNOWN DEPUY PINNACLE HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KXA·July 9, 2014