BEUDAMED
    10 results · 24ms · Sources: EU EUDAMED, US FDA

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    Klassic Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N ANTISERA TO HUMAN TRANSFERRIN

    FDA 510(k)
    FDA Class 2 ·Immunology

    EMBRYO VIEWER SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Widex

    FDA UDI
    Widex A/S·05706069793000·Widex UNIQUE U-PA (Lime green ) 100, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069819106·Widex UNIQUE U-FS (Lime green ) 100, Telecoil, ...

    PROTECTA XT DR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·June 8, 2013

    HYALGAN

    FDA Adverse Event
    Injury ·FIDIA FARMACEUTICI S.P.A.·Product code MOZ·June 23, 2011

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD., UK·Product code KWY·September 8, 2008

    iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015

    ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023