BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 15, 2012

    NA

    FDA Adverse Event
    Malfunction ·STERILMED, INC.·Product code NLQ·January 22, 2014

    CAPSURE EPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·August 10, 2010

    NEURO SPG-1X1"-STERILE- 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·February 20, 2025

    NEURO SPNG-1/2X3"-STRL- 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025

    NEURO-SP-1/2X1/2"-STRL 20/CS

    FDA Adverse Event
    Malfunction ·MEDSORB DOMINICANA, S.A.·Product code EFQ·February 7, 2025