BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    SAS SALMONELLA E,N,X ANTISERUM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Zuma™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981037659·Trial, 32mm x 25mm x 14mm, 8 Deg. Zuma™ Trials ...

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221118097·3M™ Victory Series™ Second Molar Bands, 955-214...

    CAT-3 CATECHOLAMINE ASSAY KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    IMMULITE (TM) TOTAL T3

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·February 11, 2013

    FORTIFY DR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·January 10, 2011

    INTERSTIM

    FDA Adverse Event
    Malfunction ·NEURO - VILLALBA·Product code EZW·July 24, 2014

    Allura Exper FD Series. System codes 722003 722010 722022 722005 722011 722019 722001 722002 722006 722012 722008 722013 722020 722025 722015 722023 722038 889006 889016 889009 722005 The device is an X-Ray Generator.

    FDA Enforcement
    Class II ·Terminated·Philips North America, LLC·March 25, 2020