BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    XIDF-AWS801, Angio Workstation, v5.31

    FDA 510(k)
    FDA Class 2 ·Radiology

    PASS LP SPINAL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CDX DIGITAL X-RAY IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    PASS LP - LIGAPASS

    FDA Adverse Event
    Injury ·MEDICREA INTERNATIONAL·Product code JDQ·April 26, 2013

    PASS LP

    FDA Adverse Event
    Injury ·MEDICREA INTERNATIONAL·Product code MNI·July 12, 2013

    SOLYX SIS SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 3, 2013

    AED PRO

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 17, 2011

    ASCENSION MRH

    FDA Adverse Event
    Injury ·ASCENSION ORTHOPEDICS, INC.·Product code KWI·August 26, 2008

    PASS LP - LIAPASS

    FDA Adverse Event
    Injury ·MEDICREA TECHNOLOGIES·Product code MNI·March 29, 2013