BEUDAMED
    6 results · 33ms · 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.
    Filters Regulation: Us FDA ×

    HANDIDAM

    FDA 510(k)
    FDA Class 1 ·Dental

    WAKO(TM) IGM-HA DIRECT

    FDA 510(k)
    FDA Class 2 ·Immunology

    SCI-PRO, PROPHYLAXIS PASTE

    FDA 510(k)
    FDA Class 1 ·Dental

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 19, 2014

    BONE SCREWS, CROSS-PIN, MP, SELF-DRILLING, 2,0X4MM

    FDA Adverse Event
    Other ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code JEY·October 25, 2010

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 3, 2012