BEUDAMED
    7 results · 27ms · 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.

    ACE INTRA COMPARTMENTAL PRESSURE MONITOR

    FDA 510(k)
    FDA Unclassified ·Unknown

    g.Estim PRO

    FDA 510(k)
    FDA Class 2 ·Neurology

    SHEFFIELD PHARMACEUTICALS (STERILE) LUBRIGEL

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 16, 2014

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·December 14, 2012

    PUMP MMT-523NAP PRDGM INSULIN PURPLE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·October 13, 2010

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·December 11, 2024