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

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    G21 SpaceFlex Hip

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bernafon

    FDA UDI
    Bernafon AG·05711584087152·ZR1, KIT 312 2.4G NFM 85 L BE ZERENA 1

    9.2MHZ PENCIL PROBE 10'

    FDA UDI
    PARKS MEDICAL ELECTRONICS, INC.·00816787021509·

    AIXPLORER

    FDA 510(k)
    FDA Class 2 ·Radiology

    STELLAR FIDUCIAL MARKER, MODEL GFMIA

    FDA 510(k)
    FDA Class 2 ·Radiology

    RESTORE ADVANCED RECHARGEABLE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·October 7, 2008

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 20, 2013

    FILTER, INTRAVENOUS,PALL POSIDYNE ELD

    FDA Adverse Event
    Malfunction ·PALL POSIDYNE ELD, INTRAVENOUS FILTER·Product code FPB·July 30, 2011