BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    AQUA TRAP

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    PRE VUE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    C.L.E.D. MEDIUM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    LOGIC TIBIA PS MOD INSRT SZ 2 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 16, 2024

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·May 28, 2014

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 15, 2012

    SOLETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·September 9, 2010