BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    ESOPHAGEAL Z-STENT

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

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113126·PS Insert, Size 2 x 18mm

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113189·STERILIZING CASE SMALL KATENA IOP

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110935·STERILIZING CASE NARROW

    SNAP EEG MONITOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    TEK USA E-GENERATOR INTEGRATED LED HANDPIECE (HIGH & LOW SPEED AIR TURBNINE DENTAL HANDPIECE)

    FDA 510(k)
    FDA Class 1 ·Dental

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CHD·December 10, 2010

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 8, 2014

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·December 17, 2012

    HUMAPEN ERGO TEAL/CLEAR

    FDA Adverse Event
    Injury ·ELI LILLY AND COMPANY·Product code FMF·March 17, 2017