BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    COMPUTE-RX-COMP (TM)

    FDA 510(k)
    FDA Class 2 ·Radiology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756991889·ANGIO PACK

    PIONEER SPINAL PROCESS FUSION PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO TITANIUM TRI-LOCK HIPS STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ANGIO PACK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code OEQ·March 1, 2021

    ARCHITECT C4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·July 31, 2018

    HEART START XL

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 7, 2013

    GUT SURGICAL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAL·November 24, 2010

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·July 2, 2014

    HYBRID INSERTION HANDLE

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HSB·November 12, 2019