BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    GENESIS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ArgenZ HT+ 95x20 OM1

    FDA UDI
    ARGEN CORPORATION, THE·D818122768·Dental porcelain/ceramic restoration kit

    SECRMARK BIOPSY SITE MARKING SYSTEM

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

    AMT POLYAXIAL PEDICLE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 21, 2013

    RAPIDPOINT 405

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code GKR·September 26, 2014

    DEPUY ASR XL FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·June 3, 2011