BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    POWDER-FREE NITRILE EXAMINATION GLOVE, BLUE OR WHITE (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    COPRAN ZR/ORIGIN YZ

    FDA 510(k)
    FDA Class 2 ·Dental

    Magnetom Sola, Magnetom Altea and Magnetom Sola Fit

    FDA 510(k)
    FDA Class 2 ·Radiology

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 5, 2014

    ANKLE ARTHRODESIS NAIL, LEFT 10X150MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·July 8, 2010

    RENEW RECEIVER KIT, 16-CHANNEL

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·February 4, 2015

    ATTUNE RP TIB BASE SZ 4 CEM

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code NJL·December 11, 2019

    NGAGE NITINOL STONE EXTRACTOR

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FFL·September 18, 2017

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 4, 2013

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LWS·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014