BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    ORTHORALIX 9200, ORTHORALIX 9200 PLUS, ORTHORALIX 9200 CEPH, ORTHORALIX 9200 PLUS CEPH

    FDA 510(k)
    FDA Class 2 ·Dental

    MODEL 3500 MR-COMPATIBLE PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DMI PC HOLTER SCANNER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANCHOR FAST ORAL ENDOTRACHEAL TUBE FASTENER # 9799

    FDA Adverse Event
    Injury ·HOLLISTER, INC.·Product code CBH·March 1, 2013

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·January 14, 2011

    CAPSURE Z NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014