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

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    Filters Regulation: Us FDA ×

    MODIFICATION TO LUCENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CERALOY SOLDER

    FDA 510(k)
    FDA Class 2 ·Dental

    STREERABLE PTCA GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PVA FOAM EMBOLIZATION PARTICLES

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·March 26, 2018

    ASR ACETABULAR CUPS 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 29, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·April 5, 2011

    UNK

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·July 23, 2008