BEUDAMED
    184 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·December 4, 2008

    ULTRAPULSE ENCORE

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·September 16, 2011

    ENDOPATH XCEL

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·July 29, 2013

    AMS INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·October 31, 2013

    DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code NVN·August 11, 2023

    VISIAN ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·January 15, 2013

    2.4MM TI CORTEX SCREW SLF-TPNGWITH T8 STARDRIVE RECESS 12MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·May 3, 2013

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·July 18, 2012

    UNK VISCOELASTIC

    FDA Adverse Event
    Injury ·ALCON - BELGIUM / S.A. ALCON - COUVREUR N.V.·Product code LZP·February 22, 2012

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·June 8, 2012

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·June 21, 2012

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·June 14, 2012

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·July 20, 2012

    ANTERIOR CHAMBER LENS

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·July 20, 2012

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 16, 2012

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·January 30, 2012

    ASR UNI FEMORAL IMPL SIZE 46

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 20, 2012

    ICL (IMPLANTABLE COLLAMER LENS)

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code MTA·December 7, 2016

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD/ HUNTINGTON·Product code HQL·May 21, 2012

    OPTI-FREE REPLENISH

    FDA Adverse Event
    Injury ·ALCON - FORT WORTH / ALCON LABORATORIES, INC.·Product code LPN·May 25, 2012