BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    JUDO 1 Guidewire, JUDO 3 Guidewire, JUDO 6 Guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JET-X BAR SYSTEM CLAMPS AND POSTS REPROCESSING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ULTRA SURGICAL GOWN & FLUID BARRIER SURGICAL GOWN

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    REAMER SHAFT, MOD. TRINKLE BIXCUT 8.0 X 284 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·December 18, 2012

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS·Product code MUZ·June 20, 2013

    EON MINI 16-CHANNEL RECHARGEABLE IPG

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 7, 2011

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC. USA·Product code LFR·September 22, 2008

    BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·July 22, 2018