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

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    Filters Regulation: Us FDA ×

    SAS ROTA TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SUBCUTANEOUS TISSUE EXPANDER

    FDA 510(k)
    FDA Unclassified ·Unknown

    Comus Locking Plate systems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEPUY ASR FEM IMPLANT SZ 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·March 5, 2013

    ENRHYTHM DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    Sof-Flex Multi-Lenqth Ureteral Stent Set, Global Product No. G14773 G15000 G14867 G14951 G17852

    FDA Enforcement
    Class II ·Terminated·Cook Inc.·February 12, 2020