BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    ULTRASOUND SYSTEM SONIMAGE HS1, LINEAR PROBE L18-4, CONVEX PROBE C5-2

    FDA 510(k)
    FDA Class 2 ·Radiology

    DEBAKEY DOYEN INTESTINAL CLAMP FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896024113·DEBAKEY DOYEN INTESTINAL CLAMP FORCEPS STRAIGHT...

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CGA·April 28, 2000

    BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE REGENERATION

    FDA 510(k)
    FDA Class 2 ·Dental

    MEMOMETAL INTRA-MEDULLARY BONE FASTENER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD ECLIPSE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·November 13, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 5, 2014

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 29, 2013

    UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·May 26, 2011