BEUDAMED
    6 results · 20ms · 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 ×

    P.F.C. TOTAL HIP SYSTEM POROUS COATED MODULAR ACET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UUHC REPROCESSED COMPRESSION SLEEVE DEVICES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNICEL DXC SYNCHRON SYSTEMS GLUCOSE REAGENT (GLUH)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·November 11, 2010

    S-ROM*SLEEVE PRX ZTT, 18D-SML

    FDA Adverse Event
    Injury ·DEPUY IRELAND·Product code LPH·January 28, 2013

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·July 14, 2014