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

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    PMT Expandable Cage (PMT EXP)

    FDA 510(k)
    FDA Unclassified ·Unknown

    HHM

    FDA UDI
    Sbo Hearing A/S·05714464029235·HHM F500 MINIRITE T C044

    Adler Instrument Company

    FDA UDI
    Adler, Inc.·00810123205844·Wheeler Plaque Tissue FCPS, TW 2.0mm

    SCANORA 3DX

    FDA 510(k)
    FDA Class 2 ·Radiology

    FLEXIBLE RUBBER ELECTRODES, MODELS: 1460265, 1460272, 1460274, 3444128, 3444129, 3444130

    FDA 510(k)
    FDA Class 2 ·Neurology

    ETHILON NYLON SUTURE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·November 6, 2014

    UNICEL ® DXC600I SYNCHRON ® ACCESS ® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code MMI·September 1, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 16, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025