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

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    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    PRISMA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

    *

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00346

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    Endo Carry-on Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964152207·Endo Carry-on Procedure Kit contains Basin, Enz...

    EsFlow B2 Syringe

    FDA UDI
    Spident Co., Ltd.·08809262954760·Nano-hybrid Flowable composite resin for poster...

    Single Use Biliary Stent V

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170185830·Single Use Biliary Stent V

    Kalitec Special

    FDA UDI
    Kalitec Direct LLC·B073DRK0100050·Tap, 6.5mm Cann, Quarter Square

    CYNOSURE PHOTOGENICA DL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    KAVO K.E.Y. LASER 1242

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019

    STERLING¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·March 19, 2013

    HAKIM PROG VALVE INLINE SIPHONGUARD

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC., MEDOS S.A.·Product code JXG·March 3, 2011

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008

    Kendall MONOJECT MAGELLAN 12cc Syringe with Safety Needle 20G X 1.5 inch Product Number: 5551822015

    FDA Recall
    Terminated ·Kendall Healthcare Products Co·Product code FMI·October 8, 2004