BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    STERRAD 100 STERILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ROBICSEK PROBE/RETRACTOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RICHARD-ALLAN CLAMP COVERS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    UNKNOWN DEPUY CEMENT

    FDA Adverse Event
    Injury ·DEPUY CMW ¿ REG. # 9610921·Product code LOD·January 15, 2013

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·July 7, 2014

    HS HAND CONTROLLED CURVED SHEA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GEI·February 4, 2008