BEUDAMED
    9 results · 28ms · 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 ×

    BISFIL-II(CHEMICAL CURABLE POSTERIOR/ANTERIOR)

    FDA 510(k)
    FDA Class 2 ·Dental

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690129950·Retaining Bolt, Congruent or Ultra Insert, Revi...

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707030829·WEB 1ST MOL BANDS W/G8325-03 UL 2

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209114306·

    DEPUY CMW 1 GENTAMICIN BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SkinStylus SteriLock MicroSystem (MP1209SL)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·June 6, 2014

    ECHELON*FLEX60

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 30, 2012

    ACCU-CHEK ® INFORM TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 5, 2010