BEUDAMED
    13 results · 21ms · 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 ×

    Rio Vial-to-Bag Drug Reconstitution Device

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583033044·ET20, KIT 312 NFM 90 PB R BE ENCHANT 20

    HEARTWAY POWER MOBILITY SCOOTER, S9

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TYRO-97 (HOFOCON A), ONSI 56 (HOFOCON), RIGID GAS PERMEABLE SPHERICAL, ASPHERIC, TORIC AND BIFOCAL CONTACT LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MEDFUSION

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·April 17, 2023

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 4, 2011

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code NVN·January 13, 2014

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·June 20, 2013

    1823260-2017-02143

    FDA Adverse Event
    Malfunction ·September 29, 2017

    1823260-2017-00779

    FDA Adverse Event
    Malfunction ·April 14, 2017

    1823260-2017-02426

    FDA Adverse Event
    Malfunction ·October 26, 2017

    1823260-2017-02427

    FDA Adverse Event
    Malfunction ·October 26, 2017

    COBAS 6000 E 601 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 10, 2017