BEUDAMED
    6 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.

    CUP BIOPSY FORCEP, 1.7MM

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

    IRON SET, ITEM NO. 65008

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MODIFICATION TO VERTEBROPLASTIC RADIOPAQUE BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 17, 2014

    IMPLANTABLE CHF PULSE GENERATOR

    FDA Adverse Event
    Product code NIK·October 16, 2010

    12.6CM TAPERED ATTACHMENT, BLACK MAX

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code HSZ·December 11, 2012