BEUDAMED
    8,189 results · 35ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code DQK·September 24, 2025

    SILK SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·March 27, 2023

    SILK SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·March 27, 2023

    SILK SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·March 27, 2023

    SILK SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·March 27, 2023

    SILK SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·March 27, 2023

    SILK SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·March 27, 2023

    SILK SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAP·March 27, 2023

    TYTIN

    FDA Adverse Event
    Malfunction ·KERR CORPORATION·Product code DZS·April 9, 2014

    TYTIN

    FDA Adverse Event
    Malfunction ·KERR CORPORATION·Product code DZS·April 9, 2014

    TYTIN

    FDA Adverse Event
    Malfunction ·KERR CORPORATION·Product code DZS·April 9, 2014

    TYTIN

    FDA Adverse Event
    Malfunction ·KERR CORPORATION·Product code DZS·October 16, 2014

    TYTIN

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code DZS·January 19, 2012

    TYTIN

    FDA Adverse Event
    Malfunction ·KERR CORPORATION·Product code DZS·October 16, 2014

    TYTIN

    FDA Adverse Event
    Malfunction ·KERR CORPORATION·Product code DZS·October 16, 2014

    LADARVISION

    FDA Adverse Event
    Injury ·ALCON - ORLANDO TECHNOLOGY CENTER·Product code DZS·April 25, 2007

    LADAR6000 SYSTEM

    FDA Adverse Event
    Injury ·ALCON - ORLANDO TECHNOLOGY CENTER·Product code DZS·April 25, 2007

    SILHOUETTE IC IMPLANT

    FDA Adverse Event
    Other ·BIOLET INTERNATIONAL INC.·Product code DZS·May 4, 2007

    LASER HEX IMPLANT

    FDA Adverse Event
    Other ·BIOLOK INTERNATIONAL, INC.·Product code DZS·May 4, 2007

    TYTIN REGULAR SET SPHERICAL SILVER AMALGAM

    FDA Adverse Event
    Malfunction ·KERR CORP.·Product code DZS·August 14, 1997