BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    SUPERCATH 5 (26G)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO SPACE CPSXL BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    HYLAMER 10D 56 OR 68ODX32ID

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDIC·Product code JDI·June 17, 2013

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code MMI·July 22, 2011

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code LFL·September 22, 2008