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

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    NUVO VERDE LED LIGHTING SYSTEM

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

    OAKLEY, INC.

    FDA registration
    OAKLEY, INC.·4 products·🇺🇸 United States

    COMPOSIX KUGEL MESH, MODEL 0010201,0010202,0010203,0010204,0010205

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

    TCI-31 LIFELONG OVULATION TESTER

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    D 903 AVANT ADULT HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·February 27, 2014

    CP840442 DE LEIPZIG

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·May 12, 2010

    D903 DIDECO AVANT 2 VAVD PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·February 19, 2014

    CP025369 DE LEIPZIG

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·August 3, 2011

    CP85315 IT MODENA

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·January 14, 2013

    IT PADOVA

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·August 8, 2013

    CP84050 FR LA REUNION

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·May 17, 2012

    CP84042 DE LEIPZIG %

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DWE·April 20, 2011

    D905 DIDECO EOS SINGLE HVR

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·September 25, 2013

    D903 DIDECO AVANT VAVD PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·August 16, 2013

    NORIAN ROTARY MIXER

    FDA Adverse Event
    Malfunction ·NORIAN·Product code MQV·April 29, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·May 10, 2011

    RENASYS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.·Product code JWH·July 29, 2008

    C20441 IL HAIFA

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·March 28, 2012

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC.·Product code FTL·June 14, 2011

    D905 EOS OXYGENATOR (PHISIO TREATED)

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·July 13, 2018