BEUDAMED
    9 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 ×

    CLINITRON ELEXIS

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    OSOM HCG COMBO TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Acumed Ankle Plating System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARTICULEZE M HEAD 36MM +12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·February 5, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 1, 2011

    UNKNOWN DEPUY SZ. 28X32 10 DEG LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code KWA·July 18, 2014

    FLEXNAV DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code NPT·May 13, 2024

    1.5MM SYSTEM 4 HOLE LONG STRAIGHT PLATE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·December 12, 2017

    NAVITOR TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NPT·May 13, 2024