BEUDAMED
    7 results · 24ms · Sources: EU EUDAMED, US FDA

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    Sterile Products of the APTUS System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 6, 2002

    PERIFIX CATHETER CONNECTOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KERATOR

    FDA 510(k)
    FDA Class 2 ·Dental

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·November 4, 2008

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·September 1, 2011

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 17, 2013