BEUDAMED
    20 results · 61ms · Sources: EU EUDAMED, US FDA

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    INVISALIGN

    FDA Adverse Event
    Other ·ALIGN TECHNOLOGY, INC.·Product code NXC·March 13, 2012

    INVISALIGN SYSTEM

    FDA Adverse Event
    Other ·ALIGN TECHNOLOGY, INC.·Product code NXC·January 11, 2011

    BALLOON MINI ONE BUTTON

    FDA Adverse Event
    Other ·APPLIED MEDICAL TECHNOLOGY, INC.·Product code KNT·February 13, 2013

    INVISALIGN SYSTEM

    FDA Adverse Event
    Other ·ALIGN TECHNOLOGY, INC.·Product code NXC·January 11, 2011

    RELIEVA ULTIRRA SINUS BALLOON CATHETER

    FDA Adverse Event
    Other ·ACCLARENT·Product code LRC·July 10, 2013

    I.T.I LSF ACETABULAR CUP LINER

    FDA Adverse Event
    Other ·OSTEOIMPLANT TECHNOLOGY INC·Product code KWB·May 18, 1999

    ORASURE ORAL SPECIMEN COLLECTION DEVICE

    FDA Adverse Event
    Other ·ORASURE TECHNOLOGIES, INC.·Product code LIO·August 24, 2006

    7F FRCEZOR CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Other ·CRYOCATH TECHNOLOGIES, INC.·Product code NFC·July 13, 2005

    THERAPYNOTES (ELECTRONIC HEALTH RECORD)

    FDA Adverse Event
    Other ·UNKNOWN·Product code SAP·March 23, 2026

    ADVANTIM TOTAL CONDYLAR TIBIAL INSERT

    FDA Adverse Event
    Other ·WRIGHT MED TECHNOLOGY, INC.·Product code JWH·April 5, 2011

    RELIEVA ULTIRRA SINUS BALLOON CATHETER

    FDA Adverse Event
    Other ·ACCLARENT·Product code LRC·May 10, 2013

    RELIEVA SPIN SINUPLASTY SYSTEM

    FDA Adverse Event
    Other ·ACCLARENT·Product code LRC·April 11, 2013

    INDEPENDENCE IBOT 4000 MOBILITY SYSTEM

    FDA Adverse Event
    Other ·INDEPENDENCE TECHNOLOGY, L.L.C.·Product code IMK·March 3, 2008

    MINI ONE

    FDA Adverse Event
    Other ·APPLIED MEDICAL·Product code KNT·January 9, 2013

    RELIEVA SPIN SINUPLASTY SYSTEM

    FDA Adverse Event
    Other ·ACCLARENT·Product code LRC·February 25, 2013

    INDEPENDENCE IBOT 4000 MOBILITY SYSTEM

    FDA Adverse Event
    Other ·INDEPENDENCE TECHNOLOGY, L.L.C.·Product code IMK·June 30, 2008

    GT, MINI-ONE

    FDA Adverse Event
    Other ·Product code KNT·October 26, 2011

    REHABILICARE

    FDA Adverse Event
    Other ·REHABILICARE·Product code LIH·October 16, 2005

    PLUM XL PLS MIC/MAC

    FDA Adverse Event
    Other ·HOSPIRA, INC.·Product code FRN·June 17, 2010

    RELIEVA SOLO PRO BALLOON CATHTER

    FDA Adverse Event
    Other ·ACCLARENT·Product code LRC·June 10, 2013