BEUDAMED
    869 results · 31ms · Sources: EU EUDAMED, US FDA

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    BIOTENE MOUTH SPRAY (ORIGINAL)

    FDA Adverse Event
    Other ·ULTRADENT PRODUCTS INC/ORA TECH LLC·Product code LFD·October 14, 2015

    BIOTENE MOUTH SPRAY (SAVANNAH)

    FDA Adverse Event
    Other ·ULTRADENT PRODUCTS, INC./ORA TECH LLC·Product code LFD·October 9, 2015

    ORA-50 RF GENERATOR

    FDA Adverse Event
    Other ·ORATEC INTERVENTIONS, INC.·Product code GEI·September 22, 1999

    OLYMPUS THUNDERBEAT 5MM, 35CM, PISTOL GRIP

    FDA Adverse Event
    Other ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GEI·September 22, 2012

    2.4X10MM STERNALOCK SELF DRILLING SCREW

    FDA Adverse Event
    Other ·BIOMET MICROFIXATION·Product code HWC·October 2, 2008

    2.4X12MM STERNALOCK SELF DRILLING SCREW

    FDA Adverse Event
    Other ·BIOMET MICROFIXATION·Product code HWC·October 2, 2008

    MAND INF MED DISTRACTOR

    FDA Adverse Event
    Other ·BIOMET MICROFIXATION·Product code JEY·January 15, 2009

    NAVIGATION SOFTWARE 1.6.3 SMITH & NEPHEW

    FDA Adverse Event
    Other ·BRAINLAB AG·Product code HAW·June 20, 2011

    LATEX EXAM GLOVES

    FDA Adverse Event
    Other ·ALLEGIANCE HEALTHCARE CORP·Product code LYY·July 30, 1998

    INTROCAN SAFETY

    FDA Adverse Event
    Other ·B. BRAUN MEDICAL INC.·Product code FOZ·February 10, 2006

    INTROCAN SAFETY

    FDA Adverse Event
    Other ·B. BRAUN MEDICAL INC.·Product code FOZ·February 10, 2006

    BRAINLAB KNEE NAVIGATION SYSTEM (BONE FIXATOR)

    FDA Adverse Event
    Other ·BRAINLAB AG·Product code OLO·October 31, 2012

    YELLOFIN STIRRUPS

    FDA Adverse Event
    Other ·THE OR GROUP·Product code FWZ·January 2, 2003

    YELLOFIN STIRRUPS

    FDA Adverse Event
    Other ·THE OR GROUP·Product code FWZ·January 13, 2003

    MEDTRONIC

    FDA Adverse Event
    Other ·MEDTRONIC·Product code KNS·September 6, 2005

    M3 MICRO-MLC FOR SIEMENS

    FDA Adverse Event
    Other ·BRAINLAB AG·Product code IYE·August 8, 2011

    UV-ABSORBING COLLAMER FOLDABLE INTRAOCULAR LENS.

    FDA Adverse Event
    Other ·STAAR SURGICAL COMPANY·Product code HQL·November 29, 2001

    KLI

    FDA Adverse Event
    Other ·ACMI CORPORATION·Product code KNS·January 26, 2005

    2.4MM STERNALOCK 12 HOLE, LADDER PLATE

    FDA Adverse Event
    Other ·BIOMET MICROFIXATION, INC.·Product code HRS·March 27, 2008

    STOCKERT 70 RF ABLATION GENERATOR

    FDA Adverse Event
    Other ·STOCKERT GMBH·Product code LPB·March 25, 2004