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

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    AMERICAN DILATATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209117963·KIT, IFAK - CUSTOM

    ANATOMICAL SHOULDER INVERSE/REVERSE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Med-Tainer Single Deposit Container

    FDA 510(k)
    FDA Class 2 ·General Hospital

    REPLY

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code NVZ·June 6, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·October 5, 2010

    INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·November 30, 2012

    ANATOMICAL SHOULDER REVERSE, HUMERAL CUP, 0°, RETRO

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSD·November 21, 2018

    ANATOMICAL SHOULDER REVERSE, SCREW SYSTEM, 4.5-18

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWT·November 21, 2018

    ANATOMICAL SHOULDER REVERSE, HUMERAL INSERT, PE, 36-0

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWS·November 21, 2018

    ANATOMICAL SHOULDER FRACTURE, HUMERAL STEM, 7-130

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWS·November 21, 2018