BEUDAMED
    13 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    DLP CORONARY OSTIAL PERFUSION CANNULAE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACCESS THYROGLOBULIN REAGENTS ON THE ACCESS IMMUNOASSAY SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Immunology

    ELITTECH CLINICAL SYSTEMS ALP IFCC SL

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LAB BOVIE PENCIL

    FDA Adverse Event
    Malfunction ·COVIDIEN VALLEY·Product code GEI·April 17, 2008

    VERSAFITCUP CC TRIO CUP O 50 MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL, SA·Product code LZO·December 18, 2013

    PROLENE POLYPROPYLENE SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAW·January 23, 2009

    PROLENE POLYPROPYLENE SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAW·January 23, 2009

    PROLENE POLYPROPYLENE SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAW·January 23, 2009

    NONE

    FDA Adverse Event
    MEDTRONIC EMERGENCY RESPONSE SYSTEMS·Product code LDD·May 5, 2006

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 1, 2014

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC·Product code GAS·June 16, 2011

    MOZEC¿ RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·September 20, 2022

    MOZEC¿ RX PTCA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·September 20, 2022