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 ×

    MCCAIN INSTRUMENT TMJ/SM. JOINT ARTHROSCOPIC SURG

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARRHYTHMIA CENTRAL-OGP-7201

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PERCUTANEOUS NEPHROSTOMY SETS (SCHULLER)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 16, 2014

    VENTAK PRIZM

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 19, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 16, 2012