BEUDAMED
    8 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.

    NICOLET EMG SATELLITE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    NA

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573024223·PROTRACTION FACE MASK 1/PK

    IMMULISA ANTI-BETA2 GLYCOPROTEIN I (B2GP1) IGM ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    AIRSONETT AIR-4

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HIRES 90K IMPLANT

    FDA Adverse Event
    Injury ·ADVANCED BIONICS LLC·Product code MCM·May 5, 2014

    PENUMBRA SYSTEM ASPIRATION PUMP

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code BTA·March 15, 2010

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·November 13, 2012

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018