BEUDAMED
    10 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.
    Filters Regulation: Us FDA ×

    URINE REAGENT STRIPS-3 PARAMETERS (MODIFICATION)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Zuma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981096847·Rasp, 32mm x 25mm x 18mm, 12 Deg

    3 TO 1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 14, 2011

    3-TO-1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHMAND·Product code DTQ·December 14, 2011

    FEEDING TUBE Y-PORT CONNECTOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NORMLGEL PROTECTIVE WOUND GEL

    FDA 510(k)
    FDA Unclassified ·Unknown

    VITROS 350 CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·November 27, 2017

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 11, 2013

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·January 10, 2011

    MDA ASSEMBLY

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 13, 2013