BEUDAMED
    56 results · 27ms · Sources: EU EUDAMED, US FDA

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    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL·Product code HQL·June 15, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    COLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

    BIORAPTOR KNOTLESS SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW INC MANSFIELD MANUFACTURING SITE·Product code MBI·March 5, 2013

    EVERA XT VR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 7, 2014

    STERLING BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·February 15, 2011

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

    FDA Adverse Event
    Injury ·STAAR SURGICAL CO.·Product code HQL·June 21, 2006

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIEC

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 9, 2021

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·September 29, 2021

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·January 27, 2023

    HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 13, 2022

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·May 13, 2021

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·June 17, 2021

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·November 9, 2021

    MEDTRONIC SURGICAL TISSUE VALVE

    FDA Adverse Event
    Injury ·HEART VALVES SANTA ANA·Product code DYE·June 14, 2021