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

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    1-Step Culture Medium

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SLEEVE WITH ZIPLOOP FIXATION DEVICES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VITAL SERUM CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 19, 2020

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 14, 2013

    ENDOPATH XCEL BLUNT TIP TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·October 9, 2008

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·August 4, 2011

    CD HORIZON ASTUTE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code NQP·April 16, 2021