BEUDAMED
    8 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 ×

    SURESKIN THIN

    FDA 510(k)
    FDA Unclassified ·Unknown

    Eye Shield

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111161·FOX EYE SHIELD GARTERS WHITE PACK OF 50

    McKesson

    FDA UDI
    MCKESSON MEDICAL-SURGICAL INC.·00612479205383·Exam Shorts NON-WOVEN | BLUE xx-Large (25/bg,...

    AG-PLUS, MODEL 91210

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BI-CENTRIC SYSTEM

    FDA 510(k)
    FDA Class 1 ·Dental

    OBTAPE TRANSOBTURATOR SLING

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code OTN·February 1, 2013

    MICROFRANCE® INSTRUMENT

    FDA Adverse Event
    Malfunction ·XOMED MICROFRANCE MFG·Product code GEI·July 28, 2014

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·January 13, 2011