BEUDAMED
    6 results · 18ms · 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 ×

    P.F.C.(TM) MODULAR KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODEL EEG 4400 WITH OPTIONAL ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Neurology

    MICRO-BETA U100 SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR

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

    ALTRX +4 NEUT 36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 22, 2010

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 3, 2012