BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    LUXTEC FIBEROPTIC CABLES

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    ESCOTEK-EST 221 VACUUM UNIT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    YD STRIP GPH U21

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PLATINUM PLUS?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code DQX·June 10, 2014

    TOTALCARE BARIATRIC

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·October 4, 2010

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 6, 2012

    PINN SECTOR HA ACET CUP 50MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·June 17, 2013

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·June 17, 2013

    CORAIL2 LAT COXA VARA SIZE 11

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS 3003895575·Product code KWA·October 10, 2013