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

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    CREATININE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704287776·RONGEURS CASPAR INTRAVERTEBRAL DISK 5 X 14 MILL...

    3 TO 1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 14, 2011

    3-TO-1 REDUCTION DRIVE

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHMAND·Product code DTQ·December 14, 2011

    BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS

    FDA 510(k)
    FDA Unclassified ·Unknown

    RESPIRONICS MONARCH MINI MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PORTEX SILICONISED PVC SOFT-SEAL CUFF ORAL/NASAL

    FDA Adverse Event
    Injury ·SMITHS HEALTHCARE MANUFACTURING S.A. DE C.V.·Product code BTR·February 8, 2024

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·February 11, 2013

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 24, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 10, 2011

    ev3 Pipeline Flex Embolization Device. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020